| Miltenyi Biotec Inc. |
|
|
9/4/2010
|
| Technical Sales Consultant |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=367955
|
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Sr. Scientist - Pharmacology |
| Job Requirements and Qualifications
Education: PhD with training in pathology, cell biology or related fields, expertise in oncology preferred but not required.
Must have at least 5 years experience in biotech/pharmaceutical industry.
Strong experimental skills in human disease model development, mammalian tissue culture, vector transduction and imaging-related technology.
Oncology experience is preferred. Experience in IHC is a plus.
A thorough understanding of molecular oncology and immunology.
Demonstrated experience in in vivo human disease model and an excellent publication record.
Supervisory experience preferred.
Excellent organizational, time management, communication, and interpersonal skills.
Strong oral and written skills, and experience maintaining a record of studies in the form of notebooks, technical reports, summaries, protocols, and quantitative analyses.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Some travel may be required.
|
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Senior Clinical Quality Assurance Specialist |
| Job Requirements and Qualifications
BA/BS degree in biological sciences, nursing or related discipline, or equivalent experience required
Strong knowledge of government regulations, guidelines and standards for investigation of new pharmaceutical products is required
Experience in QA audits of Clinical Investigators
Experience in QA audits of Clinical documents associated with clinical trials
Experience in system/process audits
Experience in development of SOPs
Working knowledge and understanding of drug development and global clinical regulatory environment
Ability to manage multiple projects
Effective organizational skills
Effective team player and detail oriented
Strong attention to detail, good organizational skills, ability to work independently
Solid oral and written communication skills with ability to communicate effectively and professionally with medical personnel
Knowledge Requirements:
Knowledge of the code of federal regulations, European Directives, ICH/GCP practices. The candidate will also have a working knowledge of clinical auditing processes. Previous participation in regulatory inspections is a plus.
Experience:
A minimum of 3-5 years working experience as a clinical quality assurance auditor.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 25-35%
|
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/4/2010
|
| Medical Strategist |
| Knowledge and Skills
MD
Ideally internal medicine background with broad range of experience, especially in oncology and neuropsychiatry
Ideally, agency, med-ed and/or pharma industry experience
CommonHealth is an equal opportunity employer
|
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/4/2010
|
| Medical Writer |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD, PharmD, MD) oncology experience required
Knowledge of assigned therapeutic areas
Experience writing peer-reviewed articles, distilling complex technical information for a variety of medical audiences
Familiarity with RefMan or similar database program, Word, PowerPoint
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
Problem Solving
Balancing work quality with timelines
Adopting the writing style to the target audience
Managerial Direction
Make decisions regarding content and style in consultation with program management and account management
Self management to adhere to agreed T&E schedules, budgets, and to alert team to potential deviations and overages
We are an equal opportunity employer
|
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/4/2010
|
| Medical Director |
| Requirements:
2+ years experience in patient care or medical education
Advanced degree in biomedical sciences (PharmD, PhD, MD)
Developing educational concepts and content through critical analysis of data, distilling complex technical information for a variety of medical audiences, working with opinion leaders
Knowledge of CME procedures
Writing proposals
Editing documents
Clinical research and publication experience is a plus.
Ability to provide independent medical direction
Strong written and verbal communication and presentation skills.
Software: Microsoft Word, PowerPoint, reference database programs such as Refman
Familiarity or interest in pharmaceutical marketing
Must work well in a team-oriented environment
Ability to meet deadlines while working on multiple, parallel projects
Develop solid understanding of the market and goals advocated by the medical and marketing clients
We are an equal opportunity employer.
|
| Boston Scientific |
Valencia |
CA |
9/3/2010
|
| Marketing Manager |
| Experience:
· Prefer minimum of 3 years experience in a medical-related industry in a product management, sales or marketing position with product launch experience.
· Field medical sales, technical and/or marketing communications experiences a plus.
SPECIALIZED KNOWLEDGE & SKILLS:
· Must have excellent communication skills, including the ability to listen to clinical and customer needs, prioritize needs/requirements and communicate them to cross-functional teams, including physicians.
· Must have exceptional leadership, presentation, negotiation and interpersonal skills, particularly in working effectively as a member of a team.
· Must be able to work in a fast paced environment and foster constructive relationships with internal and external customers.
· Must have excellent and professional written and verbal skills.
· Must have excellent analytical skills.
· Must have good presentation skills.
EDUCATION and TRAINING:
· Bachelor’s degree
· MBA preferred
PHYSICAL ENVIRONMENT / WORKING CONDITIONS:
· Must have the ability to handle the stresses of 25% or more travel schedule. Ability to independently manage a moderate travel schedule. Ability to be flexible in working extended schedules, including some weekends.
RESPONSIBILITY FOR PERSONNEL:
Direct Supervision: None
Indirect Supervision: None
INTERNAL CONTACTS: All levels of Sales, Engineering, Management staff, department heads, Marketing, Purchasing, Finance, Human Resources, QA, Regulatory and Clinical staff.
EXTERNAL CONTACTS:
Vendors: Vendors for all types of marketing services used in the development and promotion of medical devices; specifically, advertising agencies, market research firms, sales training organizations, graphics developers, etc.
Consultants: Scientific and health care industry consultants.
Customers: Clinicians (Referring Physicians, Implanting Physicians, Allied Health Care Providers), Hospitals and Hospital Systems, Patients, Payer Organizations, etc.
Other: University Professors and Research groups working in the Bioengineering field and the Implantable Device field.
Boston Scientific is an Equal Opportunity Employer, EEO/AA
|
| Sysmex |
Mundelein |
IL |
9/3/2010
|
| Manager, Technical Assistance Manager |
| 4- Year Bachelor's Degree in Medical Technology or Biomedical Engineering - Operations management experience and direct or indirect experience working in the clinical laboratory environment. Call Center experience helpful, technical troubleshooting with medical diagnostic equipment a plus. Demonstrated analytical and technical skills used in strategic planning and forecasting using MS Excel/database knowledge. The successful candidate must be able to communicate effectively with all levels in the organization. Strong project and team management skills required.
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. |
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/4/2010
|
| Medical Oncology Copywriter |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD or PharmD) oncology experience required
Knowledge of assigned therapeutic areas
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
Problem Solving
Balancing work quality with timelines
Adopting the writing style to the target audience
Managerial Direction
Make decisions regarding content and style in consultation with program management and account management
Self management to adhere to agreed T&E schedules, budgets, and to alert team to potential deviations and overages
We offer a competitive salary, excellent benefits, and a great working environment.
We are an equal opportunity employer.
|
| Sysmex |
Mundelein |
IL |
9/3/2010
|
| Director of Hematology, Marketing |
Find a Better Way...
...to use your skills and experience.
This is the time to let your talent come to life. To maximize your knowledge and use it for the greater good. To work with the best professionals using state-of-the-art technology, and improve lives with your innovative ideas and ambitious dreams. Find a better way: the Sysmex Way.
...to improve the lives of others.
Headquartered in Kobe, Japan, Sysmex America is located in Mundelein, Illinois. Renowned worldwide for the very finest in quality, innovative diagnostic equipment and information-management systems, we apply science to enhance the quality of life on a global scale. Our agile, resourceful team is committed to realizing critical breakthroughs in laboratory diagnostics, information technology, workflow analysis and life sciences for the clinical laboratory.
...to build a promising future.
We currently have a great opportunity available for a Director of Hematology, Marketing. This position is accountable for managing and marketing all hematology instrument, urinalysis, complementary instrument product lines plus reagents and controls. The position is responsible for creating "best of breed" marketing and sales programs, product life cycle management, promotional material, competitive material and developing thought leaders and marketplace influencers to assist Sysmex in achieving their business objectives. To provide in-depth market and industry knowledge, competitive analysis to assist in developing product and market business plans to achieve sales and market share goals. Establish a core of resident Sysmex technical and product knowledge for existing and competitive products. Launch new product to Sysmex commercial operations that achieve mid-term plan goals. The Director of Hematology proactively communicates and works in alignment with all departments within Sysmex, conducts all activities with professional demeanor, within legal, regulatory and Sysmex standards. The Director should demonstrate a positive attitude, strong interpersonal skills, an ability to manage products and people, complete projects within establishes time-lines to meet departmental and company objectives, determine market data needs and obtain necessary sales and marketing data in order to make good business decisions. The position is responsible for all aspects of the management and personnel development of a Hematology Marketing Team.
Essential Duties and Responsibilities: - Lead a marketing team of product management staff, responsible for management and development of personnel.
- Product Life Cycle Management of existing and future Sysmex Hematology instruments. Product Life Cycle Management of Urinalysis, Digital Imaging and Erythrocyte Sedimentation Product Lines.
- Analyze complex diagnostic healthcare marketplace and customer data, anticipate future marketplace trends, prepare strategies to support Sysmex America sales and financial targets.
- Internal and external champion for the Sysmex IVD product lines, providing technical, tactical and scientific marketing support to all departments within Sysmex America Inc.
- Lead new product launch teams, leading cross functional teams to introduce new products to the marketplace.
- Develop anti-competitive, scientific and market information to be used by Sysmex Customer facing staff.
- Develop sales programs to support Sysmex sales targets and financial objectives.
- Develop and monitor forecasts for hematology instrument, reagent and control product lines.
- Provide information to R&D and Sysmex Corporation on US market trends, current and future customer requirements. Participate on global Sysmex IVD product teams and committees as required.
- Provide strong leadership, develop and retain successful product management staff, communicate at all levels of the organization on marketing trends and analysis, product information and marketing programs.
- Other duties as required.
 Language Skills: No foreign language skills required; international travel experience desirable
Computer Skills: MS Office, including moderate to advanced PowerPoint
Communication Skills: Solid oral and written communications skills, presentation and influencing skills, and the ability to deal directly with professional and managerial level customers
Other Skills: Experience in project management, product management, advertising & promotion, tradeshows, market research, vendor relationships and team leadership.
Decision Making Ability: Ability to provide justification for capital and expense budget items.
Project Management Ability: Ability to lead project teams.
Problem-Solving Ability: Ability to solve complex marketing problems, including integration of marketing campaigns
Other Abilities: Self-starter with the ability to work independently and as part of a team.
Education/Knowledge Required: B.S. in Marketing, Biological Science or Physical Science; MBA highly desirable
Certificates, Licenses, Registrations: MLT, MT or equivalent highly desirable
Experience Level: 10-15 Years Experience in IVD Marketing or Sales Experience Other Qualifications Proven business-to-business marketing and team management experience. Knowledge of clinical laboratory instrumentation preferably Hematology, in vitro diagnostic market and/or LIS.
Find a better way—and make the world a better place with a company that cares: Sysmex.
You'll be rewarded with competitive compensation and benefits, as well as a highly progressive, team environment where ideas are treated like gold, and people truly matter. Learn more about us, and about your own ability to succeed.
Visit us on-line at:
http://www.sysmex.com/us/467.htm
(NO THIRD PARTY)
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. |
| Miltenyi Biotec Inc. |
|
|
9/3/2010
|
| Flow Cytometry Sales Specialist |
| Ph.D., M.S., or B.S. degree in biological sciences, immunology, molecular biology, or similar field with 5 to 8 years related experience with a minimum of 3 years of flow cytometry experience; or equivalent combination of education and experience. Prefer sales experience in capital equipment or diagnostic instruments.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA |
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/3/2010
|
| Medical Oncology Copywriter |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD or PharmD) oncology experience required
Knowledge of assigned therapeutic areas
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
We offer a competitive salary, excellent benefits, and a great working environment.
We are an equal opportunity employer
|
| Optimer Pharmaceuticals Inc, Inc |
San Diego |
CA |
9/4/2010
|
| Senior Medical Director of Pharmacovigilance |
| Educational/Experience Requirements
•MD degree with a minimum of five years industry experience in drug safety surveillance and pharmacovigilance.
•Experience in development of risk management plans is essential.
•Knowledge of global pharmaceutical regulations and guidances highly desirable.
•Clinical experience and sound medical judgment,
•Excellent analytical skills and the ability to both write and review medical reports.
•Excellent written and oral communication skills.
•Excellent interpersonal, organizational, and team-building skills.
Interested candidates e-mail resume and include job title in subject line to:
careers@optimerpharma.com
About Optimer Pharmaceuticals
Optimer Pharmaceuticals, Inc. is a biopharmaceutical company focused on discovering, developing and commercializing innovative anti-infective products to treat serious infections and address unmet medical needs. Optimer has two late-stage anti-infective product candidates under development. Fidaxomicin, formerly known as OPT-80, is the only antibiotic therapy currently in Phase 3 worldwide clinical development for Clostridium difficile infection. Pruvel™ (prulifloxacin) is an antibiotic which has completed two Phase 3 clinical trials for the treatment of infectious diarrhea in travelers. Additional information can be found at http://www.optimerpharma.com
|
| Custom Learning Designs |
Belmont |
MA |
9/3/2010
|
| Medical Director |
| • Ability to understand a medical topic in depth and apply that knowledge to creating high-quality medical content
• Review medical content for content accuracy, appropriate use of references, and clarity of information
• Produce high-quality scientific writing and demonstrate fastidious attention to detail
• Provide direction to internal staff on the creation of well-designed, accurate, medical content
• Ability to work under deadline pressures and juggle multiple projects
• Assist in proposal development and client presentations and meetings, requiring occasional travel
Qualifications:
• MD, PharmD, or PhD in life sciences or related field with expertise in multiple therapeutic areas
• Familiarity with drug development and medical, legal, and regulatory review a plus
• Computer literacy |
| Miltenyi Biotec Inc. |
Auburn |
CA |
9/4/2010
|
| Marketing Product Manager |
| Requirements:
Bachelor’s or graduate degree in the life sciences, Ph.D. or MBA preferred. Candidates must have in-depth technical knowledge and 5 years of experience in Immunology/Hematology; or equivalent combination of education and industry experience.
We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply go to: https://home.eease.com/recruit/?id=490467 |
| Kardium, Inc. |
Richmond |
British Columbia |
9/4/2010
|
| Director, Regulatory Affairs and Quality Assurance |
| The successful candidate will have:
• Strong project management, problem-solving, and negotiating skills
• Ability to execute tasks with minimal instruction and guidance
• Skill at analyzing and summarizing data.
• Ability to write clear, understandable technical documentation.
• Extreme attention to detail.
• Ability to manage and prioritize multiple projects.
• A track record of being highly productive
• Strong drive to succeed
• Experience building and leading a team
The successful candidate will preferably have:
• Participated in the implementation of an ISO 13485 quality system
• 4-year degree in a scientific or technical discipline; advanced degree helpful
• 3-5 years of regulatory experience in the biotechnology industry
• Strong working knowledge of medical devices regulations (FDA, EU, and Health Canada)
• Experience bringing a Class III device through a PMA process
If you are interested in such a position, please send an email with your resume to jobs@kardium.com with a subject line of "Director, Regulatory Affairs and Quality Assurance |
| Kardium, Inc. |
Richmond |
C02 |
9/3/2010
|
| Biomedical Engineer (Cardiovascular Devices) – Join a Fast Growing Medical Device Company! |
| Candidate profile:
• A solid background in biomedical engineering with industry R&D experience
• Experience with medical image segmentation, processing, and analysis
• Experience in Design of Experiments (DoE) and statistics
• Mechanical design background with hands-on experience in both laboratories and machine shops
• Superior math and physics skills
• Experience with SolidWorks, Matlab, and LabView
• The ability to coordinate activities within a multi-disciplinary team
• Familiarity with medical device regulatory affairs and quality systems
Responsibilities:
• The design and execution of experiments serving to characterize, refine, and optimize device designs regarding device function and performance.
• Coordination and documentation of cadaver and in vivo device testing conducted off-site
• Acquisition and analysis of medical imaging datasets to build knowledge of heart chamber size and morphology
• Collaboration with mechanical, software, and electronics engineering teams to provide them with input and feedback on device designs
• Development of analytical tools to help interpret test results
• Work in the clinic to better understand user and therapeutic system requirements
The Biomedical Engineer position is an on-site role located in Vancouver, Canada. Vancouver, home of the 2010 Winter Olympic and Paralympic Games, is a vibrant and diverse urban center surrounded by abundant natural attractions. The city is internationally ranked as one of the ‘Best Places To Live’ by the Mercer Consulting Quality of Living Survey.
To apply for this position, please email your resume to jobs@kardium.com with a subject line of "Biomedical Engineer (Cardiovascular Devices)". |
| Sysmex |
Houston |
TX |
9/4/2010
|
| Health Systems Application Specialist |
The qualified candidate we seek must possess the following: - Bachelors Degree in Clinical Laboratory Science. Medical Technologist degree
- Working knowledge and solid CLIA/COLA experience
- Strong Hematology experience preferred.
- ASCP or CLS certification required
- 3-5 Years Experience (Supervisory experience highly desirable)
- Proficient with Microsoft Suite; PowerPoint, Excel, Word, Internet Explorer
- Strong written and oral communications skills required. Highly visible position to the external customer requiring extensive interpersonal contact. Professional conduct necessary at all times even under stressful conditions.
- Strong presentation and persuasive skills highly desirable.
- Demonstrated ability to analyze and evaluate technical data. Ability to assemble thoughts and conclusions into cogent and persuasive format, present professionally and gain acceptance / buy-in.
- Demonstrated ability to plan moderately complex technical evaluations and projects. (e.g. instrument evaluations / implementations)
- Demonstrated ability to both independently and collaboratively solve complex technical and reagent problems (e.g. instrument trouble shooting)
Find a better way and make the world a better place with a company that cares: Sysmex.
You'll be rewarded with competitive compensation and benefits, as well as a highly progressive, team environment where ideas are treated like gold, and people truly matter. Learn more about us, and about your own ability to succeed.
Visit us on-line at:
http://www.sysmex.com/us/467.htm
(NO THIRD PARTY)
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing.
APPLY ONLINE |
| Sysmex |
Mundelein |
IL |
9/4/2010
|
| Inside Sales Manager |
Qualified Candidate Criteria: - Bachelors degree, with 5 plus sales experience and 3 years sales management experience.
- CRM experience a plus. Professional, concise communication skills required to allow confirmation of potential customer needs and present viable solutions.
- English, Spanish a plus. Must have exceptional written and verbal communication skills. Must be able to interact effectively with various members of a wide range of departments within the company. Ability to work well with others in a professional manner.
Find a better way and make the world a better place with a company that cares: Sysmex. You'll be rewarded with competitive compensation and benefits, as well as a highly progressive, team environment where ideas are treated like gold, and people truly matter. Learn more about us, and about your own ability to succeed.
Visit us on-line at: www.sysmex.com/us/467.htm
-NO THIRD PARTIES-
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. |
| Sysmex |
Mundelein |
IL |
9/4/2010
|
| Inside Sales Representative |
Qualified Candidate Criteria: - Bachelors degree preferred or equivalent experience
- Minimum of 1-2 years sales experience
- Experience with CRM system, MS Office
- Professional, clear communicator allowing confirmation of potential customer needs and present viable solutions
- Language skills: English, Spanish a plus
- Ability to interact effectively with various members of a wide range of department within the company
- Ability to work well with others in a professional manner
Find a better way and make the world a better place with a company that cares: Sysmex. You'll be rewarded with competitive compensation and benefits, as well as a highly progressive, team environment where ideas are treated like gold, and people truly matter. Learn more about us, and about your own ability to succeed.
Visit us on-line at: www.sysmex.com/us/467.htm
-NO THIRD PARTIES-
We are proud to be an EEO/AA employer M/F/D/V. We maintain a drug-free workplace and perform pre-employment substance abuse testing. |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Manager, Cost Accounting |
| • Must have a BS degree in Accounting & at least 10 years accounting experience.
• Must have at least 5+ years manufacturing experience with strong knowledge of SAP.
• A CPA or CMA is preferred but not required.
• Must be proficient in excel and have strong communication skills in all levels of management.
• Must have supervisory experience and work independently.
• Must be a self starter and be highly motivated. |
| Shimadzu Scientific Instruments, Inc. |
Pleasanton |
CA |
9/4/2010
|
| Field Service Engineer |
| A minimum of an AA in Electrical Engineering or Technology (BA in a Life Science Field preferred) with 3 years of field exposure with related instrument repair or the equivalent experience.
Incumbent should have knowledge of electronics, SSI Product Lines, Strong Organizational and Customer relationship Skills and be computer literate. |
| Shimadzu Scientific Instruments, Inc. |
Madison |
WI |
9/3/2010
|
| Field Service Engineer |
| A minimum of an AA in Electrical Engineering (Balcehlor's in a Life Science preferred) or Technology with 3 years of field exposure with related instrument repair or the equivalent experience.
Incumbent should have knowledge of electronics, SSI Product Lines, Strong Organizational and Customer relationship Skills and be computer literate. |
| Shimadzu Scientific Instruments, Inc. |
Los Angeles |
CA |
9/3/2010
|
| Field service Engineer |
| A minimum of an AA in Electrical Engineering (a bachelor's in a Life Science preferred) or Technology with 3 years of field exposure with related instrument repair or the equivalent experience.
Incumbent should have knowledge of electronics, SSI Product Lines, Strong Organizational and Customer relationship Skills and be computer literate. |
| Shimadzu Scientific Instruments, Inc. |
Raleigh/Durham |
NC |
9/3/2010
|
| Life Science Account Manager |
| A minimum of a B.S. degree in Chemistry, or a closely related field, at least two (2) years of laboratory experience, five + (5) years of LCMS/GCMS experience. Sales experience is a plus but not a requirement.
The incumbent must have excellent problem solving, technical, application and operational skills related to Chemistry and Mass Spectrometers; in order to solve customer and regional problems and ensure customer satisfaction. |
| Shimadzu Scientific Instruments, Inc. |
Baltimore |
MD |
9/3/2010
|
| Field Sales Engineer- Analytical Instrumentation |
| A Degree in one of the Life Sciences, three years successful sales experience with one or more of our equivalent product lines and the individual must possess a valid driver’s license.
Expertise and thorough knowledge needed in the operation of all analytical instruments, strong sales skills, time and territorial management and computer literacy. A working knowledge in report preparation, chemistry, customer relations, and telemarketing is required. |
| Shimadzu Scientific Instruments, Inc. |
Columbia |
MD |
9/3/2010
|
| Product Specialist - Liquid Chromatography |
| Incumbent must be proficient at effectively troubleshooting operational, application and other instrument problems in a methodical efficient manner. Additionally, incumbent must be able to act independently in matters not governed by policy to ensure customer satisfaction. Incumbent must have a Bachelor’s degree in the physical or natural sciences with at least two years of technical applications experience in the appropriate product line (HPLC) or the equivalent experience in maintenance and/or repair of analytical instrumentation.
Please visit our website for a complete job description and to use our apply online feature - www.ssi.shimadzu.com/employment.
SSI is an EOE -M/F/D/V |
| Eveo |
San Francisco |
CA |
9/4/2010
|
| Scientific Content Director |
| EXPERIENCE/SKILLS REQUIREMENTS
- Advanced life science (PhD, PharmD, MS) or medical (MD, DO) degree;
- 5+ years managing science content development within an agency focused on the pharma/biotech space, preferably digital
- 10+ years’ medical/scientific writing/editing experience
Job Description:
http://docs.google.com/View?id=dqfmzsf_10fzfw9tgv |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Manager, Cost Accounting |
| Scope Measures
This position will have an impact on the future pilot plant’s operating & capital budgets, headcount within their function, newly created policies and procedures related to the pilot plant. This position will also make decisions and have an impact on the configuration of the SAP & LIMS configuration related to the cost accounting manufacturing environment.
Knowledge/Skills/Abilities Required
• Must have a BS degree in Accounting & at least 10 years accounting experience.
• Must have at least 5+ years manufacturing experience with strong knowledge of SAP.
• A CPA or CMA is preferred but not required.
• Must be proficient in excel and have strong communication skills in all levels of management.
• Must have supervisory experience and work independently.
• Must be a self starter and be highly motivated. |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Director, Downstream Operations |
| Scope Measures
The individual will play a critical role in the commissioning, startup, and routine operation of the Morphotek pilot plant whose purpose is to produce material for toxicology, and phase I and phase II clinical trials to support Morphotek’s clinical development pipeline. Specifically, this person will contribute to the success of the operation by ensuring that the downstream suites, equipment, staff and infrastructure can support manufacture of materials for global clinical supplies. The individual will also be responsible to maintain and/or enhance the production area systems and technology to remain compliant to regulations and to ensure successful transfer of new products in development.
Knowledge/Skills/Abilities Required
• BS, MS or PhD in biological sciences or engineering
• 10-15 yrs of practical scientific experience
• Minimum of 10 yrs in a multi-discipline cGMP environment, commissioning and managing downstream production areas.
• Knowledgeable in purification, formulation, downstream equipment operation, and CIP/SIP operations.
• Knowledgeable in technology transfer, equipment scale-up, equipment validation and facility startup.
• Ability to identify, investigate, and solve process and equipment problems.
• Strong working knowledge of cGMP, EMEA, and JP regulations.
• Excellent written and communication skills.
• Excellent interpersonal skills.
• Team player who can excel in a “hands-on” entrepreneurial environment.
• Ability to supervise, mentor, train, and develop staff |
| Shimadzu Scientific Instruments, Inc. |
Columbia |
MD |
9/4/2010
|
| Product Coordinator/Molecular Spectroscopist |
| Incumbent must be proficient at effectively troubleshooting operational, application and other instrument problems in a methodical efficient manner. Additionally, incumbent must be able to act independently in matters not governed by policy to ensure customer satisfaction. Incumbent must have a Bachelor’s degree in the physical or natural sciences with at least seven years of technical applications experience in the appropriate product line or the equivalent experience in maintenance and/or repair of analytical instrumentation. |
| openQ |
Charlottesville |
VA |
9/3/2010
|
| Data Services Project Manager |
| Skills:
• Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics
• Solid understanding and experience with spreadsheet programs
• Excellent verbal and written communication skills
• Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control
• Prior experience interfacing with customers about data-related projects
• Strong team player and the proven ability to work independently
Education:
• Minimum of Masters level degree in life sciences field (PhD preferred) and at least 3 years relevant experience in a life sciences-driven data company.
|
| Shimadzu Scientific Instruments, Inc. |
Baton Rouge |
LA |
9/4/2010
|
| Field Service Engineer - Analytical Instrumentation |
| KNOWLEDGE REQUIREMENT:
Incumbent should have knowledge of electronics, SSI Product Lines, Strong Organizational and Customer relationship Skills and be computer literate.
EDUCATION AND/OR EXPERIENCE:
A minimum of an AA in Electrical Engineering or Technology with 3 years of field exposure with related instrument repair or the equivalent experience.
|
| Miltenyi Biotec Inc. |
Oakland |
CA |
9/3/2010
|
| Technical Sales Consultant - Bay Area, CA |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=517835 |
| Snowdon, Inc |
Monmouth Junction |
NJ |
9/3/2010
|
| Medicinal Chemist |
| The successful candidate will have a BS/MS in organic or medicinal chemistry and have had at least 5 years experience in an industrial drug discovery organization.
Snowdon seeks highly motivated scientists with exceptional communication and presentation skills, who can excel in a highly goal-oriented entrepreneurial atmosphere. To be considered for this position, please send a cover letter, resume and research summary (no more than 5 pages) to humanresources@snowdonpharma.com. No relocation will be offered; local candidates only, please.
|
| Chantest |
Cleveland |
OH |
9/3/2010
|
| Staff Scientist - Electrophysiology |
| Minimum qualifications are a BS/BA in biology, chemistry or related science with at least one year of laboratory experience. Prior experience in an electrophysiology laboratory is a plus, but is not required.
ChanTest provides a competitive benefits package. Salary is commensurate with experience. Please send your resume with salary requirement to: humanresources@chantest.com or fax to 216-332-1706. Equal Employment Opportunity. |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Oncology Business Planning / Senior Manager, Demand Innovation |
| Knowledge/Skills/Abilities Required
• BA/BS in Marketing or Business Related Field
• 5-7 Years of progressive commercial experience in the biotech/pharmaceutical industry with a minimum of 2 or more years in the Oncology specialty
• Self motivated and passionate about Oncology and the goals of the Morphotek PCU
• Domestic & International Travel Required >50%
• Candidate must work from Morphotek offices unless traveling for business related duties
• Must have permanent work authorization in the U.S. |
| Morphotek®, Inc. |
Exton |
PA |
9/4/2010
|
| Senior Scientist, Antibody Core Development |
| Knowledge/Skills/Abilities Required
• Ph.D., 3 years post-doctoral experience
• Strong background and expertise in molecular biology, recombinant protein or antibody expression and purification (bacterial and mammalian) as well as biochemical and functional characterization of proteins and antibodies is required.
• Familiarity with GS expression systems, FACS analysis, Vector NTI software, Robotics systems/programming, and QPCR light cycler a plus. |
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/3/2010
|
| VP Management Supervsior |
| Must have at least:
•8+ years in business
•8+ years marketing advertising agency experience on professional marketing accounts
•6+ years in healthcare/pharmaceutical marketing
•6+ years as a leader of account management personnel
•Minimum four (4) year degree required; Master’s Degree/MBA a plus
•Strong knowledge of the pharmaceutical and healthcare industry
•Oncology experience preferred, prostate experience a plus
•Outstanding leadership skills
•Outstanding team building skills
•Experience managing a brand and coordinating multiple disciplines required (i.e. professional, consumer, digital, med ed)
•Innovative thinker who also has the ability to foster innovative thinking in others
•Proven relationship building with client Brand Managers, Team Leaders, and Directors of Marketing (or equivalent)
•Can point to meaningful successes that they have "owned"
•Track record of innovative business solutions and successes
•Excellent communication, presentation and time management skills
•Writes extremely well -- writes presentation decks on their own
•Sound financial skills -- has prepared budgets, staffing plans, and statement/scope of work plans
•Centrally engaged in the agency process (not a peripheral player or bench-warmer)
•Detail-oriented, drives for results
•High strategic fluency
•High digital fluency
•Production and process fluency – must be able to help with process when necessary
•Experience working within a pharmaceutical company is a plus
•Launch experience a must
•Microsoft Excel and PowerPoint proficiency is a plus
We are an equal opportunity employer. |
| Miltenyi Biotec Inc. |
San Diego |
CA |
9/3/2010
|
| Technical Sales Consultant - San Diego |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=502699 |
| Ogilvy CommonHealth Worldwide |
Parsippany |
NJ |
9/4/2010
|
| EVP Level Managing Director |
| Must have at least:
•20+ years in business
•10+ years marketing advertising agency experience on professional marketing accounts
•5+ years in healthcare/pharmaceutical marketing
•5+ years as a leader of account management personnel
•Minimum four (4) year degree required; Master’s Degree/MBA a plus
•Strong knowledge of the pharmaceutical and healthcare industry
•Experience in working with and leading multi-faceted teams and managing multiple businesses
•Outstanding leadership skills
•Outstanding team-building skills
•Ability to be both a great team leader and a great teammate
•Demonstratable experience as a "change agent' in current position
•Proven relationship building with senior executive level clients
•Can point to meaningful successes that they have "owned"
•Excellent communication, presentation and time management skills
•Writes extremely well -- writes presentation decks on their own
•Sound financial skills -- understands basic accounting principles and can read and understand financial reports
•Centrally engaged in the agency process (not a peripheral player or bench-warmer)
•Detail-oriented, drives for results
•Ability to work in a matrix
•Very high strategic fluency
•High digital fluency
•Production and process fluency – must be able to help with process when necessary
•Experience managing a brand and coordinating multiple disciplines required (i.e. professional, consumer, digital, Med Ed, CRM, Managed Markets)
•Experience working within a pharmaceutical company is a plus
•Relevant therapeutic category experience is a plus
•Some proficiency in Microsoft Excel a plus |
| HireLifeScience.com |
Somerset |
NJ |
9/4/2010
|
| The HireLifeScience.com Career Fair - 9/21/10 |
| Required qualifications to attend:
Candidates must possess a 4 year life science related degree and 2 years professional experience working for a Life Science related company. You may pre-register at http://career.hirelifescience.com/ An invitation to attend will be sent if the minimum qualifications are met. |
| New England Biolabs, Inc. (NEB) |
Ipswich |
MA |
9/3/2010
|
| Director Quality Management Systems |
| The ideal candidate will have:
•Demonstrated knowledge of ISO 9001 guidelines, ISO 13485 guidelines, cGMP’s and other regulatory requirements for the manufacture, testing, and release of biological products.
•Demonstrated ability to write SOPs, quality methods and product specifications.
•Excellent written and oral communication skills, proven organizational and leadership skills, and the ability to work cooperatively in an interdisciplinary, team environment.
•Working knowledge of MS Office, SharePoint and familiarity with database design.
•Strong interpersonal skills with the ability to develop constructive and cooperative working relationships with others and maintaining them over time.
Qualifications:
•B.S/B.A. degree in Biology, Chemistry, Engineering or related science field, with a broad working knowledge of basic molecular biology techniques. A minimum of 8 years experience, preferably in the pharmaceutical or biotechnology industry, with at least 5 years of experience in Quality Assurance or Quality Control.
New England Biolabs, Inc. is an equal opportunity employer M/F/D/V
|
| New England Biolabs, Inc. (NEB) |
Ipswich |
MA |
9/3/2010
|
| Postdoctoral Fellowship – Bioinformatics |
| Qualifications:
•Ph.D. in computational biology or related field.
•A strong record of scientific publication.
•Creative data visualization skills.
•A positive attitude and a strong work ethic.
This position offers exciting opportunities for broad research training, collaboration with academic institutions, publishing in peer-reviewed journals and participation in national and international conferences.
New England Biolabs, Inc. is an equal opportunity employer M/F/D/V
|
| Miltenyi Biotec Inc. |
Orlando |
FL |
9/4/2010
|
| Technical Sales Consultant - Orlando, FL |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=521160 |
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Associate Director, CMC Regulatory |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Director, Regulatory Labeling & Promotional Compliance |
|
| Millennium Pharmaceuticals |
Boston |
MA |
9/3/2010
|
| Clinical Program Manager |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Manager, Regulatory Submission Management |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Director, IT Operations |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Clinical Research Manager II |
|
| Millennium Pharmaceuticals |
Boston |
MA |
9/3/2010
|
| Clinical Research Associate |
|
| Millennium Pharmaceuticals |
Albany |
NY |
9/3/2010
|
| Senior Manager, Global Medical Affairs Outreach |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Clinical Scientist |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr. Manager, Regulatory Submission Management |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Science Liaison - Gulf |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Assoc Director/Director of Publications |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Senior SharePoint Engineer |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Assoc Dir, Molecular Medicine |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Associate Director, International Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr. Manager/Associate Director, Labeling & Promotional Compliance |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Science Liaison - Great Lakes East |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Senior Scientist, Molecular Medicine Imaging |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| MEDICAL DIRECTOR |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Director |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Clinical Research Manager II |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr Software Engineer |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Southwest Regional Director, Medical Science Liaisons |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Director; Business Analysis & Project Management |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Dir, Strategic Clinical Sourcing |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Product Manager/Sr Product Manager |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Oncology Sales Specialist - Queens, NY |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Science Liaison - Northeast |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Medical Science Liaison - Southwest |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Post-Doc Research Fellow - Pharmacovigilance and Risk Management |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
9/3/2010
|
| Sr Research Associate |
|
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Vice President, Market Development, HAI |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer (Computer) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer (Computer) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Tubes Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| TOOLING ENGINEER |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Tig Weld thru - Cut - D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Technical Writer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Technical Service Contact Center Manager |
| See above |
| BD (Becton, Dickinson and Company) |
St. Louis |
MO |
9/3/2010
|
| Technical Applications Specialist-Research Flow Cytometry |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Systems Validation Specialist II |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Syringe Specialist-All Shifts |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer- Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Optical Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Staff Engineer or Scientist - Chemical Engineering and Biocompatibility |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Staff Engineer - Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Sr. Product Engineer (PVA Platform) |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr. Optics/Laser Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. NetWeaver Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Sr. Industrial Designer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sr. Global Marketing Manager - Tubes |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sr Systems Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Specialist - B Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Software Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Sharepoint Developer (VBScript / JavaScript) |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Setup Instruct & Repair - 2nd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Set-up Instruct and Repair B/D Shift (Reposted liting bidding restrictions for time in Job for Flush Associates) |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Set Up - D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Senior Systems Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Security Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
9/3/2010
|
| Senior Regulatory Compliance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Quality Engineer - Customer Support |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Senior Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Project Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Senior Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Senior Molding Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Senior Mechanical Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SENIOR MANUFACTURING SUPPORT ENGINEER |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Manager, Clinical Programs |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer- Electrical/Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Senior Engineer - Process/Project |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Clinical Trial Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Senior Business Partner ? Learning and BDU |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Senior Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| SECURITY OFFICER |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Scientist- Chemistry |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Scientist - In Vivo |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus East |
NE |
9/3/2010
|
| SCF Setup (Setup Instruct Repair) 2nd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SAP Technical Architect / Solutions Architect |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| SAP Security Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sales Contract Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Sales Contract Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Safety Intern |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Research Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Repair Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| R&D Manager Advanced Product Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| R&D Director, Preanalytical Diagnostics |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Quality Management Principal Engineer - Instruments |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Control Microbiology Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Quality Assurance Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| QM Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| QC Associate I - BDB |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Project Statistician |
| See above |
| BD (Becton, Dickinson and Company) |
Miami |
FL |
9/3/2010
|
| Project Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Project Manager/System Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Project Engineer R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Broken Bow |
NE |
9/3/2010
|
| Production Shift Facilitator - 12 hr shift - Blue Nights |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Production Planner II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator IV |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Product Manager - Software |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
9/3/2010
|
| Product Manager - Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Product Manager - Cell Culture Environment |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Madison |
WI |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Process and Automation Development Engineer-PosiFlush |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Principal Polymer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer- Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer, Mechanical/Environmental |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer Technical Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Principal Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Plastics Molding Engineer - Injection Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Plastics Molding Engineer - Injection Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Pilot Lab Operator III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Phone Support Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Packaging Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
9/3/2010
|
| Packaging Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Needles Setup Instruct & Repair - 1st Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Needles Coordinator - 3rd shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Needle Products Associate 3rd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Molding Technology Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Molding Process Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Mold Technician - D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Mold Maker - 1st |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Medical Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Material Handler III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Material Handler III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Material Handler III |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Material Handler III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Material Controller II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Master Data Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Marketing Communications Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
9/3/2010
|
| Manufacturing Technician I, Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
9/3/2010
|
| Manufacturing Technician I, Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manufacturing Integrator, Process Development |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
9/3/2010
|
| Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manufacturing Director - Plastics/SAIS |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Manufacturing Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
9/3/2010
|
| Manufacturing Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
9/3/2010
|
| Manufacturing Associate 1 |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manager, R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Manager, R&D |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manager, Corporate Safety and Industrial Hygiene |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Manager Software Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Manager R&D - Software Development |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Manager R&D - Mechanical Engineering and Design |
| See above |
| BD (Becton, Dickinson and Company) |
Teterboro |
NJ |
9/3/2010
|
| Manager of Flight Operations |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Manager International Taxes & Audits |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Manager Clinical Research Associates |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IT Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IT Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IT Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| IT Project Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| IT Programmer / Business Analyst - 1st shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IT Compliance Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IP Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| IP Docketing Clerk |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Inventory Control Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
San Francisco |
CA |
9/3/2010
|
| Instrument Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Instrument Assembly Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| IECO Setup, Instuct & Repair 2nd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Global IT Service Planner |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Financial Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus East |
NE |
9/3/2010
|
| Finals Inspector 3rd Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus East |
NE |
9/3/2010
|
| Finals Inspector 2nd shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Facility Technician 1st Shift |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Facilities Maintenance Technician III Electrician |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Extruder Operator |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus West |
NE |
9/3/2010
|
| Environmental Engineer - 1st Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
9/3/2010
|
| Electrical Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
9/3/2010
|
| Electrical Controls Technician I B/D Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Director, R&D, WW Self Administration of Injectable Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director, Global Medical Affairs, Advanced Treatment Technologies |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director R&D - Systems Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director R&D - Electrical and Software Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director Quality Engineering |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Director of Marketing, Prefilled Initiative |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Director of Manufacturing - Process Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Director of Global Health Policy and Practice |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Data Base Administrator II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| CRM Data Administrator |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Cost and Budget Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Commodity Specialist - Team Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Clinical Trial Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Clinical Principal Statistician |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Clinical Laboratory Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
9/3/2010
|
| Chemistry Lab Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Channel Protection Manager - Forensic Accounting |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
9/3/2010
|
| Channel Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
9/3/2010
|
| Buyer/Planner |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
9/3/2010
|
| Biological Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
9/3/2010
|
| Biochemist I - BDB |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| BDM PS US Purchasing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Back-up Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Associate Medical Director, Medical Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
9/3/2010
|
| Associate Medical Director, Medical Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Associate Medical Director |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
9/3/2010
|
| Assembly Technician I, Repair Center |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Applications Programmer (.NET) |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Regulatory Affairs Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
9/3/2010
|
| Consolidations Team Leader |
| See above |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Analyst Marketing Research |
Education/Experience Qualified candidates must have a Bachelor degree; MBA degree is desirable. Minimum of 4 years of pharmaceutical experience; and 3 years of marketing research experience is also required. Ability to proficiently use Microsoft Office tools; read, analyze, and incorporate secondary data; and analyze data tabulations are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Houston |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Houston Central, TX |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Fort Myers |
FL |
9/3/2010
|
| Hospital Sales Representative - Fort Myers, FL |
Education and Experience Guidelines:
Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence. |
| Daiichi Sankyo, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Santa Monica, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Manager, Medical Writing |
Education/Experience Qualified candidates must have a PharmD, PhD in biological sciences. MD is strongly preferred. Otherwise exceptional candidates with a MS or BS/BA may be considered. Minimum requirement of 3 years experience with PharmD or PhD, 5 years with Masters’ Degree or 7 years with a BA/BS. Experience in writing regulatory documents (protocols, Investigator Brochures [IBs], Clinical Study Reports (CSRs), clinical sections of the CTD [2.5, 2.7.3, 2.7.4], integrated summaries of efficacy and safety [ISE and ISS], briefing books, and regulatory responses) in the pharmaceutical or CRO environment required; ability to interpret and organize scientific data; and general understanding of clinical research, biostatistics, electronic publishing, and relevant industry guidelines (GCP, eCTD, and ICH). Marketing submission experience (NDAs or MAAs) preferred but not required. Daiichi Sankyo develops or has developed drugs in the following therapeutic areas: cardiovascular diseases, metabolic diseases, inflammation and immunology, infectious diseases, and oncology. Relevant therapeutic area experience preferred. Ability to quickly get up to speed on a therapeutic area, project, or indication with little to no coaching, work concurrently on several complex projects, meet aggressive deadlines, and adjust priorities rapidly as the situation demands. Strong interpersonal and communication skills (both verbal and written) are also required as the individual must be able to work in a team environment and coordinate with the team to move documents forward to completion. Must be a self-motivated person who can work with limited guidance/supervision. Excellent writing skills with a clear concise style and excellent grammar, punctuation, and spelling; proficiency in a Microsoft Windows environment; and strong MS Word skills and ability to work with templates. Excellent attention to details, especially as related to accuracy of numbers/statements and consistency within and across documents. |
| Daiichi Sankyo, Inc. |
Fredericksburg |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fredericksburg, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Syracuse |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Syracuse, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Saint Paul |
MN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Saint Paul, MN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Lead Applications Administrator, CP&A |
Education/Experience Qualified candidates must have a bachelors degree or commensurate experience and a minimum of 5 years IT experience, 2 years of experience developing and supporting web applications using Oracle, Java, Java web services, Java EJB, XML; 2 years using Oracle, SQL, PL/SQL and 2 years with application configuration, upgrades, rollout and support experience. Experience in the pharmaceutical industry, managed markets contracting, with exposure to Commercial, Medicaid, Medicare, GPO and other federal markets and with I-Many CLM and Revenue Management Suite is highly preferred. Knowledge of pharmaceutical industry pricing, contracting practices and key contract management processes (Rebates and Admin Fees, Membership) is highly preferred. Good SQL and analytical skills and the ability to evaluate user requirements and capability to design and develop solutions to meet those requirements are important in this role. Oracle SQL, PL/SQL, Web Development, DHTML, Java EJB, J2EE/Java, Java Webservices, XML and JBoss are required skills; BI Tools are a plus in this role. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Staff Biostatistician |
Education/Experience Qualified candidates must have a MS or PhD in Statistics, Biostatistics, or Mathematics. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills.Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Sales Representative, Primary Care 2 - Jacksonville West, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Albuquerque |
NM |
9/3/2010
|
| Specialty Sales Representative - Albuquerque, NM |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Massapequa |
NY |
9/3/2010
|
| Sales Representative, Primary Care 3 - Massapequa, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Walnut Creek |
CA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Walnut Creek, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Denver |
CO |
9/3/2010
|
| District Manager, Primary Care 3 - Denver, CO |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Asheboro |
NC |
9/3/2010
|
| Sales Representative, Primary Care 2 - Asheboro, NC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Lafayette |
IN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Lafayette, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Baltimore |
MD |
9/3/2010
|
| Hospital Sales Representative, Baltimore NE, MD |
Education and Experience Guidelines:
Bachelor's Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence |
| Daiichi Sankyo, Inc. |
Orange |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Orange, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr Analyst HR Technology SAP Specialist |
Education/Experience Qualified candidates must have a Bachelor's degree in Computer Science, Information Systems, or related field or commensurate experience. A minimum of 3 years experience of HRIS experience including atleast 1 year experience working with reporting in SAP HR - PA, OM, Compensation modules and creating custom queries. Proficiency or experience in PD, LSO, BW, MSS, ESS reporting is a plus. Strong knowledge of HR technology and practices, system technical architecture, office application products database elements, relationship and query concepts/report writing skills; proficient in developing queries; and writing business user specs and possess a strong understanding of relational databases are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Grand Rapids |
MI |
9/3/2010
|
| District Manager, Primary Care 3 - Grand Rapids, MI |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Human Resources Intern |
| div>Education/Experience Qualified candidates must be currently enrolled in at least their junior year of an accredited undergraduate or graduate program with a concentration in Human Resources or related field. Prior experience in a corporate business environment is preferred; experience in Human Resources Department a plus. It is required that you are proficient with Microsoft Office (Word, Excel, and Power Point). Strong interpersonal skills, communication skills (oral and written), and time management skills are essential. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Director Human Resources Business Partner - Field |
| Education/Experience Qualified candidates must have a Bachelor’s degree; Master's degree is preferred. Minimum of 10 years of progressive Human Resources experience with at least 3 years supervising HR professionals is required. Experience of the pharmaceutical industry and working with field based functions in highly preferred. You will be accountable for the confidentiality of employee data and required to travel to business area offices on a quarterly basis. Must be willing to travel 15% of the time. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Manager, National Market Analysis |
Education/Experience Qualified candidates will have a Bachelor's Degree; MBA preferred. A minimum of 5-7 years of pharmaceutical industry experience in marketing, market research or business analysis function is required. Experience in sales analysis and secondary data analysis is also essential; pharmaceutical sales experience is a plus. Qualified candidates will have excellent written and or communication skills, as well as the ability to present complex data in a clear and concise manner. Additionally, it is required that candidates have a familiarity with IMS, Wolters Kluwer, SDI, and other data sources as well as a familiarity with Business Objects and MS Access. A high level of proficiency with Microsoft Office (Word, Excel, Powerpoint, Outlook) is essential. Knowledge of databases, SPSS, and SQL (structured query language) is preferred. Must be able to travel 10% of time. |
| Daiichi Sankyo, Inc. |
Monterey |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Monterey, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| Specialty District Manager, Columbus, OH |
Requirements:
BS/BA Degree. Two or more years of Primary Care or Specialty District Management experience. |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| District Manager, Primary Care 3 - Columbus, OH |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Louisville |
KY |
9/3/2010
|
| Sales Representative, Primary Care 1 - Louisville South, KY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| District Manager, Primary Care 3 - Oklahoma City, OK |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Baltimore |
MD |
9/3/2010
|
| Sales Representative, Primary Care 3 - Baltimore West, MD |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Cruces |
NM |
9/3/2010
|
| Sales Representative, Primary Care 3 - Las Cruces, NM |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Director, Procurement |
Education/Experience Qualified candidates must have a bachelor's degree in Business, Supply Chain, Engineering or a related field with a minimum of 10 years of procurement experience including a minimum of 5 years of strategic sourcing experience or commensurate experience in related functions; MBA is preferred. Candidates must have prior experience with proven success in the implementation of procurement best practices; successfully developed and implemented effective business strategies which call for the coordination of activity from more than one functional area; and in the pharmaceutical/healthcare industry. Strong financial/analytical acumen; "Hands On” management style; and intuitive ability for critical thinking and quantitative analysis are important skills in this role. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Director, Regulatory Operations |
Education/Experience BS or MS degree in Life Sciences is essential. Experience in the pharmaceutical industry with more than 15 years of direct regulatory affairs experience. Working knowledge of laws, regulations and guidelines is essential. Experienced in filing INDs, NDAs in both paper and electronic formats. Experienced in managing an operations group. Basic computer skills (MS Word, Excel and Acrobat) are vital. Knowledge of InSight Publisher and Microsoft Project are a plus. Excellent interpersonal skills are required. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Coordinator, Organization and Talent Development |
Education/Experience Qualified candidates must have a high school degree or equivalent with a minimum of 4 years administrative office experience. Experience in a Human Resources and/or Training environment is strongly preferred. Some college experience is desired. Experience working with internal and external personnel management level is preferred. Excellent organizational and follow up skills; experience working in detailed environment; ability to prioritize and balance numerous priorities and meet deadlines in a challenging fast paced environment are critical skills in this role. Expert level knowledge of MS Office is also required. Experience using training management and newsletter software and SAP is preferred. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Chesapeake |
VA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Chesapeake, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Associate Director, Accounting |
Education/Experience Qualified candidates must have a Bachelor’s Degree in Business Administration, Finance or Accounting required, MBA and/or CPA preferred. Seven to Ten years experience in financial reporting or financial analysis and accounting combined with strong project management skills. The Finance Department's responsibilities are primarily project related in nature and require employees to demonstrate the following skills; teamwork, initiative, problem solving, creativity, and decision making abilities. Strong financial and accounting skills with equal strength in general business acumen. Strong interpersonal skills to effectively interact and influence people from other functional areas. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Sr. Director, Clinical Development, Oncology |
Education/Experience Qualified candidates must have a MD and a minimum 5 years of pharmaceutical development experience and at least 3 years of hands-on experience managing a major, multi-country, clinical program. Must be an Oncologist. Knowledge of pharmaceutical business, worldwide drug development and regulatory process. Expertise in complex clinical trial design (i.e. factorial design, etc.) and complex implementation (i.e. including Steering Committees, Safety Monitoring Boards, etc.) as well as the interpretation of scientific data. Independent thinking, creativity and innovation. Ability to deliver high quality products. Strong interpersonal skills and ability to interface effectively with multinational development teams in a multicultural working environment. Excellent communication, presentation and negotiation skills with emphasis on building consensus. Ability to effectively manage interactions with academic thought leaders ensuring optimal cooperation for achieving program and department goals. Ability to anticipate and facilitate issue resolution in a multicultural working and business environment. |
| Daiichi Sankyo, Inc. |
Allentown |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Allentown, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Vegas |
NV |
9/3/2010
|
| Sales Representative, Primary Care 3 - Las Vegas, NV |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lufkin |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Lufkin, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Des Moines |
IA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Des Moines W, IA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr. Manager, Training and Policy |
Education/Experience Qualified candidates must have a bachelor's degree and a minimum of 7 years of experience in pharmaceutical sales management, marketing management, training, instructional design, policy development or a combination of the above; ability to establish & maintain credibility and trust throughout the organization; strong writing ability and instructional design and training presentation skills; ability to analyze and synthesize information and to draw conclusions; source and manage vendors are critical skills in this role. Familiarity with pharmaceutical company training requirements; familiarity with OIG and trade association guidance documents, prosecutions and CIAs, Sentencing Guidelines and best practices for corporate compliance programs; FDA and pharma experience; sales, marketing, training and policy development experience are also required in this role. Must be willing to travel 20% of the time. |
| Daiichi Sankyo, Inc. |
Cleveland |
OH |
9/3/2010
|
| Sales Representative, Primary Care 1 - Cleveland West, OH |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Mobile |
AL |
9/3/2010
|
| Hospital Sales Representative, Mobile, AL |
Education and Experience Guidelines:
Bachelor's Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Director, Modeling and Simulation |
Education/Experience Qualified candidates must have a Ph.D. in Pharmaceutical science or equivalent. Minimum requirement 8 years clinical pharmacology and pharmacokinetics experience, including implementation of state of art modeling and simulation to support compound development. Expertise in M&S in support of cardiovascular, oncology and diabetics preferred. In-depth knowledge of current regulatory requirements (FDA, GCP and ICH). Ability to work independently and to effectively prioritize, proactively identify and resolve problems and work in a team environment. Must possess excellent communication and interpersonal skills, as well as effective collaboration and negotiation techniques. Highly proficient in standard computer software (Word, Excel and Power Point) and helpful to have proficiency in specialized software for pharmacokinetic data analysis. Demonstrated experience in population pharmacokinetic-pharmacodynamic modeling required using NONMEM. Experience in clinical trials simulation desirable. |
| Daiichi Sankyo, Inc. |
Charleston |
SC |
9/3/2010
|
| Sales Representative, Primary Care 3 - Charleston, SC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Gulfport |
MS |
9/3/2010
|
| Sales Representative, Primary Care 2 - Gulfport, MS |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Manager, Predictive Modeling |
Education/Experience: Qualified candidates must have a Bachelors degree, or an equivalent combination of education and experience in Business, Mathematics, Economics, Statistics or other discipline appropriately focused on analysis and a minimum of 5 years of pharmaceutical industry experience with 1-3 years of experience developing and maintaining forecasts and other predictive models for pharmaceutical products, marketing initiatives, and market events. Experience includes characterizing market dynamics that influence pharmaceutical product performance. High level analytical thinking and problem solving; ability to work cross functionally to incorporate a broad range of perspectives and to provide actionable outputs to all stakeholders up to executive level; advanced proficiency with Microsoft Excel (advanced functions and Visual Basic); and proficiency with presentation software are critical skills in this role. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Wichita Falls |
TX |
9/3/2010
|
| Sales Representative, Primary Care 1 - Wichita Falls, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Chico |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Chico, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Fort Lauderdale |
FL |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fort Lauderdale, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Madison |
WI |
9/3/2010
|
| Sales Representative, Primary Care 3 - Madison, WI |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Newport News |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Newport News, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Manager, Training Development |
Education/Experience Qualified candidates must have a 4 year college degree with a minimum of 5 years of pharmaceutical industry experience; minimum of 2 years pharmaceutical sales experience and a minimum of 1 year of Sales Training experience. Completion of Level 1 Trainers Certification is required; Project Management and Leadership Development is preferred. Outstanding disease state & product knowledge; excellent presentation & facilitation skills; and proficiency in MS Office Suite are required in this role. Must be willing to travel 30% of the time including field contacts, advisory board and task force meetings, National Meetings, POA meetings and additional training initiatives. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Auditor |
Education/Experience Qualified candidates must have Bachelors degree with 3 or more years auditing experience in GAAP/auditing and accounting principles. Focus in internal controls and fraud prevention is preferred. Knowledge of business processes and internal controls and experience auditing those processes for control weaknesses and reliable financial reporting; and experience conducting interviews of employees/vendors/customers is preferred. Demonstrated abilities and competencies in Sarbanes Oxley and/or J-SOX; COSO Integrated Control Framework; PCAOB Auditing Standards; IIA’s International Standards for the Professional Practice of Internal Auditing; SAS 99; and Generally Accepted Accounting Principles (GAAP) is also required. CPA or CFE and Public Accounting Experience is preferred. Must be willing to travel 15% of the time. |
| Daiichi Sankyo, Inc. |
Seattle |
WA |
9/3/2010
|
| Specialty Sales Representative, Seattle North, WA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
San Diego |
CA |
9/3/2010
|
| Sales Representative, Primary Care 3 - San Diego, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Las Cruces |
NM |
9/3/2010
|
| Sales Representative, Primary Care 1 - Las Cruces, NM |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Evanston |
IL |
9/3/2010
|
| Sales Representative, Primary Care 1 - Evanston, IL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Staff Biostatistician |
| Education/Experience Qualified candidates must have Statistics, Biostatistics, or Mathematics: MS or PhD. PhD + 8 yrs or MS + 10 years of pharmaceutical industry experience; full knowledge of advanced statistical analytical methods, clinical trial research, regulatory requirements, coding techniques, and statistical software. Excellent oral and written communication skills; project planning skills; demonstrated experience in analyzing clinical trial data; priority setting skills; multi-tasking skills; problem solving skills; eye for detail; exercise good judgment; and works well within team framework. Comprehensive project management skills. Demonstrated competency in SAS. Regular attendance at IDT Meetings is necessary; experience in managing CROs and external vendors. |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Specialty Sales Representative - Jacksonville North, FL |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Huntington |
NY |
9/3/2010
|
| Specialty Sales Representative - Huntington, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
New Rochelle |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - New Rochelle, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Kingsport |
TN |
9/3/2010
|
| Sales Representative, Primary Care 3 - Kingsport, TN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Lansdale |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Lansdale, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Westchester |
NY |
9/3/2010
|
| Hospital Sales Representative, Westchester, NY |
Education and Experience Guidelines:
Bachelor's Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence. |
| Daiichi Sankyo, Inc. |
Washington |
DC |
9/3/2010
|
| Sales Representative, Primary Care 3 - North Washington, DC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Hagerstown |
MD |
9/3/2010
|
| Sales Representative, Primary Care 1 - Hagerstown, MD |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Sales Representative, Primary Care 2 - Oklahoma City North, OK |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Year Round Information Systems Application Intern |
| Education/Experience Requirements: Qualified candidates will be currently enrolled in an undergraduate program, in at least your junior year of study; Candidates may also be in a graduate program, in an accredited program with a concentration in Information Technology along with business management or related field. Prior experience in a corporate business environment is preferred; experience in an Information Technology Department is a plus. Candidate should be good problem solvers and have understanding of basic algorithms. It is required that you have strong interpersonal, communication and time management skills as well as a proficiency in Microsoft Office (Word, Excel, and Power Point). Knowledge of using some of the following programming languages, software programs, technologies and/or skills is preferred: HTML, DHTML, JAVA, XML, CSS, and Database concepts |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Exec. Medical Dir Medical Research TA Head - Hypertension & Metabolism |
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in clinical, research or academic medicine and a minimum of 7 years of pharmaceutical industry experience; leadership experience managing scientific staff; and experience with cardiovascular medical strategies and clinical trial implementations. Advanced training in cardiovascular medicine is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Additional training in the area of cardiovascular medicine is highly desired; experience with hypertension and metabolism products are required Must be willing to travel up to 40% with up to 10% international travel. |
| Daiichi Sankyo, Inc. |
Billings |
MT |
9/3/2010
|
| Sales Representative, Primary Care 2 - Billings, MT |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
San Diego |
CA |
9/3/2010
|
| Hospital Sales Representative - San Diego, CA |
Education and Experience Guidelines:
Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence. |
| Daiichi Sankyo, Inc. |
Gulfport |
MS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Gulfport, MS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Jackson |
MS |
9/3/2010
|
| Sales Representative, Primary Care 3 - Jackson South, MS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Manager, Area Training Support |
| Education/Experience: Qualified candidates will have a 4 year college degree; Master's degree in Adult Education, Curriculum/Instruction is preferred. Society of Pharmaceutical and Biotech Trainer membership preferred. Must have the following experience: five plus years overall professional experience; two plus years pharmaceutical sales and at least one year as a Sales Trainer. We are looking for someone with demonstrated superior selling skills expertise. Must possess excellent presentation and facilitation skills, strong interpersonal skills (mentoring and coaching), and problem solving skills. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| CMO Manager |
Education/Experience Qualified candidates must have a Master's degree in biology, microbiology, biochemistry, or chemical engineering with a minimum of 5 years experience, or a Bachelor's degree with a minimum of 8 years experience of hands on clinical and/or commercial industry experience in the manufacturing science of biologics (mAbs) and/or cell based therapeutics. Interaction with contract manufacturing organizations and biotech product companies is required and technology transfer and process scale-up are a plus. The skills needed for this position are adequate knowledge of cGMPs, regulatory requirements, and CMC operations in a biotech company; and excellent negotiation and communication skills. |
| Daiichi Sankyo, Inc. |
Topeka |
KS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Topeka, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Binghamton |
AL |
9/3/2010
|
| Sales Representative, Primary Care 1 - Binghamton/Elmira, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Sacramento |
CA |
9/3/2010
|
| Sales Representative, Primary Care 2 - Sacramento West, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Pikeville |
KY |
9/3/2010
|
| Sales Representative, Primary Care 3 - Pikeville, KY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Clinical Study Manager |
Education/Experience Qualified candidates must have Bachelor’s Degree in Life Sciences or higher. A minimum of 3 years of experience in clinical research (at least 2 of these in Clinical Development) in pharmaceutical or device company, Academic Research Organization or CRO with BS. Minimum of 2 years of clinical research experience with MS, MPH, PhD or higher. Complete understanding of the concepts and applications of clinical research, medical terminology and other disciplines involved in drug development. Proficient skills in computer applications such as Word, Excel, and PowerPoint. Strong oral and written communication skills. Complete knowledge of GCP, FDA CFRs and ICH Guidelines. Ability to interpret data and to present results in a concise and clear manner. Management and leadership skills to contractors to the successful completion of the project. Working knowledge of the components and key content requirements of IND & NDAs. |
| Daiichi Sankyo, Inc. |
Salina |
KS |
9/3/2010
|
| Sales Representative, Primary Care 2 - Salina, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Senior Analyst Field Analytics |
| Education/Experience: Qualified candidates will have a Bachelor's Degree; preferably in Business Administration, Quantitative Methods, Market Research, Information Management or a related field. MBA is preferred. Candidates should have 3-5 years of experience, preferably in a Sales Operations function in the pharmaceutical industry, and 3-4 years of experience that should include report development and sales analytics. Must have systems experience with 2 of 4 of the following: decision support, data warehousing, management reporting and sales force automation. Knowledge of Pharmaceutical Syndicated Data (a plus), such as IMS’ DDD, Xponent/Xponent Plantrak and analytical software, SPSS or SAS, Dendrite SFA (a plus) and Business Objects is required. Must have demonstrated analytical skills, excellent customer service, communication, presentation, and interpersonal skills. Must be proficient in the application of personal computers and software, including extensive experience with report writing applications and the Microsoft Office Suite. Must be able to manage multiple projects effectively using multi- disciplinary resources to meet project and timeline demands and experience interacting with outside vendors. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Clinical Study Manager |
Education/Experience
Bachelor’s Degree in Life Sciences or higher. A minimum of 3 years of experience in clinical research (at least 2 of these in Clinical Development) in pharmaceutical or device company, Academic Research Organization or CRO with BS. Minimum of 2 years of clinical research experience with MS, MPH, PhD or higher. Complete understanding of the concepts and applications of clinical research, medical terminology and other disciplines involved in drug development. Proficient skills in computer applications such as Word, Excel, and PowerPoint. Strong oral and written communication skills. Complete knowledge of GCP, FDA CFRs and ICH Guidelines. Ability to interpret data and to present results in a concise and clear manner. Management and leadership skills to contractors to the successful completion of the project. Working knowledge of the components and key content requirements of IND & NDAs. |
| Daiichi Sankyo, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Sales Representative, Primary Care 3 - Oklahoma City North, OK |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Seattle |
WA |
9/3/2010
|
| Hospital Sales Representative - Seattle North, WA |
Education and Experience Guidelines:
Bachelor’s Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence. |
| Daiichi Sankyo, Inc. |
Terre Haute |
IN |
9/3/2010
|
| Sales Representative, Primary Care 2 - Terre Haute, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Exec. Medical Dir Medical Research TA Head - Oncology |
Education/Experience Qualified candidates must have a MD degree with a minimum of 10 years experience in oncology clinical, research or academic medicine and either a minimum of 7 years of pharmaceutical industry experience or 15 years experience in academic medicine with experience conducting industry sponsored trials. Experience with oncology medical strategies and clinical trial implementations are required. Leadership experience managing scientific staff is required. Subspecialty training in the area of oncology is highly desired. Experience in the business development area would be a plus. Excellent written and oral communication skills, particularly strong formal presentation skills; strong interpersonal skills commensurate with the need to work closely with outside physicians/ scientists and numerous in-house support groups; knowledge of scientific methods, research design and medical practices and procedures that would be acquired through clinical experience and clinical research studies; good understanding of the current legal and regulatory environment are critical skills in this role. Basic knowledge and appropriate application of biostatistics is required in this role. Must be willing to travel up to 40% with up to 10% international travel. |
| Daiichi Sankyo, Inc. |
Pittsburgh |
PA |
9/3/2010
|
| Hospital Sales Representative, Pittsburgh South, PA |
Education and Experience Guidelines:
Bachelor's Degree from an accredited four-year institution required; advanced degree desirable
A total of 3 years of pharmaceutical sales experience; Cardiovascular and or Hospital experience preferred
Broad healthcare market business acumen and industry knowledge. Outstanding verbal communication skills a must. Ability to self-motivate. Attention to detail. Must possess an executive presence |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Director, Biostatistics and Data Management |
Education/Experience Qualified candidates must have a MS in Statistics, Biostatistics, or Mathematics with a minimum of 15 years of pharmaceutical industry experience or a PhD in Statistics, Biostatistics, or Mathematics with a minimum of 10 years of pharmaceutical industry experience. Extensive experience analyzing clinical trial data; experience managing external contracted resources required; direct personnel management experience is preferred. The incumbent must have full knowledge of advanced statistical analytical methods, data management, clinical trial research, regulatory requirements, programming skills, and statistical software. Demonstrated mastery of advanced statistical analytical methods, competency in SAS, clinical trial search, regulatory requirements; coding techniques, protocol development and personal computing. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Administrative Assistant, Information Systems |
Education/Experience
HS diploma required; Associate’s Degree or completion of secretarial vocational program preferred. 3-5 years secretarial experience is preferred. Qualified candidates must have strong organizational ability, effective time management, excellent customer service skills, and a detail-oriented work style. In addition, good oral and written communication skills are required as well as the ability to manage multiple tasks. Proficiency in MS Office (Word, Excel, PowerPoint) and Outlook are also required. Experience providing administrative support in IT and /or the pharmaceutical industry a plus. |
| Daiichi Sankyo, Inc. |
Wilkes Barre |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Wilkes Barre, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Director, Global Project Management |
Education/Experience Qualified candidates must have a PhD degree preferred or other advanced degree (i.e., MS or MBA) with additional relevant experience. Minimum of 10 years experience in an R&D function within a biotech or pharmaceutical company with 5 years of pharmaceutical research and development project management experience, and an understanding of drug commercialization and marketing. Demonstrated experience motivating and leading project teams to completing all activities associated with managing product candidates through all stages of development and registration including submission of at least one major NDA/MAA or major supplemental regulatory submission. This includes coordinating integrated drug development plans, project team meeting minutes, and project schedules. Strong communication, negotiation, and computer skills. Working knowledge of Word, Excel, PowerPoint, and Project Management software applications. PMI or similar certification is a plus. Must be willing to travel 25% of the time. |
| Daiichi Sankyo, Inc. |
San Jose |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - San Jose, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Fond du Lac |
WI |
9/3/2010
|
| Sales Representative, Primary Care 3 - Fond du Lac, WI |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
New Orleans |
LA |
9/3/2010
|
| District Manager, Primary Care 2 - New Orleans, LA |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Chesapeake |
VA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Chesapeake, VA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oceanside |
CA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Oceanside, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Oceanside |
NJ |
9/3/2010
|
| Sales Representative, Primary Care 3 - Oceanside, CA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Worcester |
MA |
9/3/2010
|
| Specialty Sales Representative,Worcester, MA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Dallas |
TX |
9/3/2010
|
| Sales Representative, Primary Care 2 - Dallas East, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Associate Director, HEOR Biostatistics |
Education/Experience Qualified candidates must have an advanced degree in biostatistics or relevant field and a minimum of 5 years experience in the pharmaceutical industry or consulting organization. Ph.D. is preferred. Analytical experience in cardiovascular and oncology; and knowledge of cardiovascular and oncology therapeutic areas is preferred. Proficiency in data management across multiple platforms; expertise in using statistical software such as SAS and SPSS; and scientific computer programming, database querying, and descriptive and inferential statistics are required. Experience with economic modeling, multiple imputation techniques and truncated data analysis is preferred. Must be willing to travel 10% of the time. |
| Daiichi Sankyo, Inc. |
Atlanta |
GA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Atlanta West, GA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Pittsburgh |
PA |
9/3/2010
|
| Sales Representative, Primary Care 1 - Pittsburgh West, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Chicago |
IL |
9/3/2010
|
| District Manager, Hospital Sales - Chicago, IL |
Education and Experience Guidelines
BS / BA required
Five years successful pharmaceutical sales experience. A minimum of two years district manager experience; Hospital Management and Cardiovascular experience is preferred.
Must be able to travel to meetings and related sales events up to 50-70% of the time. |
| Daiichi Sankyo, Inc. |
Salina |
KS |
9/3/2010
|
| Sales Representative, Primary Care 1 - Salina, KS |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Rocky Mount |
NC |
9/3/2010
|
| Sales Representative, Primary Care 3 - Rocky Mount, NC |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Tucson |
AZ |
9/3/2010
|
| Sales Representative, Primary Care 2 - Tucson, AZ |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Johnstown |
PA |
9/3/2010
|
| Specialty Sales Representative, Johnstown, PA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Brooklyn |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Brooklyn North, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Project Data Manager |
Education/Experience Qualified candidates must have a Bachelor's degree or Registered Nurse with a minimum of 6 years pharmaceutical/data management experience or a Master's degree plus a minimum of 4 years experience in pharmaceutical/data management. Project management experience is preferred. Clinical database administration and system validation experience; CRO management experience; and demonstrated knowledge of clinical data flow and research design are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Lafayette |
IN |
9/3/2010
|
| Sales Representative, Primary Care 2 - Lafayette, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Reading |
PA |
9/3/2010
|
| Sales Representative, Primary Care 3 - Reading, PA |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Manhattan |
NY |
9/3/2010
|
| Sales Representative, Primary Care 2 - Manhattan S, NY |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Manager, Managed Markets - Customer Value Marketing |
| Education/Experience Qualified candidates must have a bachelor's degree; master's degree is preferred. Minimum of 5 years of pharmaceutical experience is required. Minimum of 1 year of pharmaceutical sales experience; minimum of 2 years of pharmaceutical managed care sales and account management; and managed markets marketing experience, marketing research or brand marketing is preferred. Clear understanding of Managed Markets customers including customers’ views on pharmaceutical co-marketing, education, and partnering initiatives with pharmaceutical companies as well as financial P&L understanding, legal, regulatory, compliance, clinical guidelines, and disease management are critical skills in this role. |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| District Manager, Primary Care 2 - Columbus, OH |
Experience and Education Requirements:
Bachelor's Degree required. Minimum 3 years Pharmaceutical sales experience. Previous management experience preferred. OR 4 years Pharmaceutical experience, with a minimum of 2 years sales experience and 2 years of home office experience (e.g. marketing, sales operations, sales training). Overnight travel up to fifty percent required. |
| Daiichi Sankyo, Inc. |
Jacksonville |
FL |
9/3/2010
|
| Sales Representative, Primary Care 2 - Jacksonville South, FL |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Director, Clinical Development |
Education/Experience Qualified candidates must have a MD with training in Internal Medicine. Subspecialty training in Endocrine and Metabolism or related therapeutic area preferred. PhD or PharmD degree candidates with extensive clinical development experience will be considered. For MD, a minimum 2 years of hands-on industry experience in drug and clinical development is required. For PhD or Pharm. D, a minimum of 4 years of clinical development is required. Knowledge of pharmaceutical business, worldwide drug development and regulatory process are preferred. Expertise in complex clinical trial design (i.e. factorial design, etc.) and complex implementation (i.e. including Steering Committees, Safety Monitoring Boards, etc.) as well as the interpretation of scientific data. Independent thinking, creativity, self starting and innovation. Ability to deliver high quality products. Strong interpersonal skills and ability to interface effectively with multinational development teams in a multicultural working environment. Excellent communication, presentation and negotiation skills with emphasis on building consensus. Ability to effectively manage interactions with academic thought leaders ensuring optimal cooperation for achieving program and department goals. Ability to anticipate and facilitate issue resolution in a multicultural working and business environment. |
| Daiichi Sankyo, Inc. |
Columbus |
OH |
9/3/2010
|
| Sales Representative, Primary Care 1 - Columbus South, OH |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Manhattan |
NY |
9/3/2010
|
| Specialty Sales Representative, Manhattan North, NY |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
Parsippany |
NJ |
9/3/2010
|
| Sr. Director Operational Excellence |
Education/Experience Qualified candidates must have a Bachelor’s Degree in Life Sciences, Chemical, Biochemical Engineering or related field; Master’s or Ph.D. preferred. Minimum of 10 years overall work experience with a a minimum of 6 years management experience in the pharmaceutical, biotech or analytical contract laboratory industries. Experience should include process development, manufacturing operations, fill/finish production support, process transfer, scale-up and troubleshooting. Management experience should include Stability, QC, Analytical R&D, direct supervision of technical staff, direction of laboratory operations, and implementation of process and system improvements. Must have strong record of managing and delivering global, cross-functional projects across multiple technologies. Skilled in transitioning support from one team to another. Knowledge of Quality by Design (QBD) and Process Analytic Technology (PAT) and demonstrated ability to apply technology solutions to business problems are required skills in this role. Strong knowledge of regulatory requirements and guidance—particularly cGMPs and a thorough understanding of SAP reporting functionality including standard and organization specific reports are required skills in this role. Active membership with ISPE, RAPS or BIO is highly desirable. Must be willing to travel 15% of the time domestically and internationally. |
| Daiichi Sankyo, Inc. |
Santa Barbara |
CA |
9/3/2010
|
| Specialty Sales Representative - Santa Barbara, CA |
Requirements:
BS/BA Degree. Two or more years of pharmaceutical sales experience. |
| Daiichi Sankyo, Inc. |
New Haven |
CT |
9/3/2010
|
| Sales Representative, Primary Care 3 - New Haven, CT |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred |
| Daiichi Sankyo, Inc. |
Edison |
NJ |
9/3/2010
|
| Project Data Manager |
Education/Experience Qualified canddiates must have a Master's degree; Bachelors degree or registered nurse in life sciences; 4 to 6 years (MS) pharmaceutical/data management; 6 to 8 years (BS/RN) pharmaceutical/data management. Project management experience is preferred. Demonstrated knowledge of clinical data flow and research design; clinical database administration and system validation experience; demonstrated competence with GCP/regional regulatory guidelines, SOPs (including WPs), medical terminology, standard coding dictionaries, and demonstrated proficiency in applying them to all relevant therapeutic areas and CRO management experience, including a thorough knowledge of CRO audits are critical skills in this role. EDC and SDTM experience is preferred. |
| Daiichi Sankyo, Inc. |
Houston |
TX |
9/3/2010
|
| Sales Representative, Primary Care 3 - Houston West, TX |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Daiichi Sankyo, Inc. |
Terre Haute |
NJ |
9/3/2010
|
| Sales Representative, Primary Care 3 - Terre Haute, IN |
Education and Experience Requirements:
BS/BA.
Pharmaceutical sales experience with a background in cardiovascular medication preferred. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Financial Analyst - Agensys, Santa Monica, CA |
| ? B.S, degree in a Accounting or business preferred.? 3 to 6 years of financial data analysis experience.? Excellent skill in manipulating Excel spreadsheets.? Ability to develop meaningful reports from complex data sources.? Strong knowledge of GAAP. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, Clinical Studies |
| B.S./B.A. life sciences degree or B.S.N or R.N. and ten years clinical research experience with four years experience in the management of people; M.S. degree and seven years related clinical research experience with four years people management experience; Pharm. D. or Ph.D. degree and five years of clinical research experience and a minimum of four years managing people. Must have excellent interpersonal skills, written and verbal communication skills, administrative skills and computer ability as well as in depth knowledge of the clinical drug development process and clinical study design and planning. He/she must be able to rapidly grasp medical concepts in a variety of therapeutic areas. Experience in project management and strategic planning is preferred. Ideal candidate will have managed a project leading to a New Drug Application or Product License Application. Candidate must also have proven management and leadership ability, knowledge of FDA/GCP requirements and familiarity with the pharmaceutical industry. Moderate (20-40%) travel required. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Clinical Research Specialist |
| University/College Degree or previous healthcare experience desired. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer abilities. Minimum travel required. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Manager, Clinical Studies |
| University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Manager, Clinical Studies, Oncology |
| University/College degree with seven years clinical trials experience is desired. Proven time and project management skills, knowledge of drug development process and proven leadership ability is required. Working knowledge of ICH and GCP guidelines is required. Experience in people management is preferred.Proven track record in oncology required. Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability. Travel required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Maintenance Mechanic - Agensys, Santa Monica, CA |
| ? A High School Diploma? Ten years relevant experience in Bio-Pharmaceutical, petrochemical, packaging or power generation industries with at least four years of that in a pharmaceutical FDA regulated GMP environment ? Demonstrated abilities and /or evidence of training in the repair, operations and troubleshooting of electromechanical process equipment, HVAC systems and utility systems? The ability to read blueprints and P&ID?s? Good communication skills verbal and written? Good computer and keyboard skills, proficient with standard business software |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, Compensation |
| Minimum of 10+ years of experience in human resources with at least seven years compensation experience. Experience in the pharmaceutical industry preferred. Requires Bachelors Degree, MBA preferred.Excellent knowledge of HR/compensation practices and principles, and all applicable labor, pay, benefits, health and safety laws and regulations. Excellent, planning, time management, communication, decision-making, presentation, organization, and interpersonal skills.Strategic business partner, good communicator with excellent interpersonal skills. Ability to communicate and present information to all levels within and outside the organization in a comprehensible manner. A team player with outstanding leadership skills. Detail oriented and accurate. Proactive. Solid mathematical aptitude and analysis skills. Knowledge of human resources automated systems. Work requires professional written and verbal communication and interpersonal skills. Ability to motivate teams to produce quality materials within tight timeframes and simultaneously manage several projects. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, Human Resources |
| Bachelor?s degree in Human Resources or Business, or equivalent experience required. Master?s degree preferred.Seven to ten years related experience required, preferably in the pharmaceutical or healthcare industries. Three to five years management experience required.Demonstrated Human Resources generalist knowledge required, specifically including employment law.Incumbent must have demonstrated ability to work in a challenging, multi-cultural work environment.Ability to manage confidential information imperative, including influencing others to maintain the confidentiality of sensitive information.Some travel required, up to 50% depending on assigned organizations. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, IT Client Relationship Management |
| Serves as the IT liaison for a specific enterprise wide business unitManages the IT resources dedicated to the business unit or functionWorks directly with the senior leadership of the business unit and IT Performs or directs high level activities with appropriate awareness of other activities within the organizationServes as a business advocate to IT and an IT advocate to the businessResolves complex business issues that affect cross functional areas or multiple sitesDirects the IT application and support requirements from a staffing perspectiveKeeps the Business and IT informed of important changes in each of the respective areas Leads complex business process reengineering projects Controls project priorities and ensures balance between business needs and IT resource constraintsResponsible for project delivery, providing ongoing updates and advocacy to the Business and IT Meets regularly with business personnel to define, review or revise:IT support strategiesApplication portfolioProject priorities and statusSystems supportApplications and infrastructure service levelsApplication growth projections and new access requirementsDirects the development and documentation of IT Strategies and Plans as a member of the IT Senior Management TeamWorking jointly with key business contact(s), manages the IT budgets, projects and prioritiesExtensive knowledge and skill through broad and/or deep experiences in Pharma IT Strong communication and interpersonal skills, capable of motivating and influencing teamsPerform at the highest levels and able to make decisions on their ownAble to translate between technical and business leaders at the highest levelsViewed as credible, and well respected by the business and IT organizationsAccountability in building and maintaining positive and cooperative working relationships Fifteen or more years of relevant experience within the pharmaceutical industry Collaboration and cross functional facilitation skillsHigh level understanding of project management, quality assurance, and IT best practicesProficiency with commercial applications that are designed to support enterprise wide business capabilitiesAdvanced Degree required (or progress towards and significant industry experience) |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Analyst, IT Quality |
| Bachelor?s Degree in Computer Science, related field, or equivalent experience required.5 + years relevant experience related to change management, document development, and application testing.Working knowledge of computer systems validation processes, system development life cycle, and Change Management processes. Must exhibit creativity and innovation in solutions; be broadly focused and able to manage multiple efforts concurrently.Exceptional attention to details and ability to consistently produce high quality and accurate work.Has solid interpersonal and communications skills (written, oral, and non-verbal) to effectively relate to technical staff and business customers.Ability to be self-directed within the scope of their duties and responsibilities.Ability to build and maintain positive and cooperative working relationships by demonstrating collaborative behaviors and cross functional facilitation skills.Understand the pharmaceutical industry and IT best practices. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Facilities Department Planner/Assistant- Agensys, Santa Monica, CA |
| ? An Associates of Arts degree? A minimum of two years experience working in a pharmaceutical FDA regulated environment? A working knowledge of Computerized Maintenance Management Systems? Self-starter with the ability to work with minimum supervision? Excellent verbal and written communication skills? The ability to multitask and exercise good judgment? The ability to work in a fast pace environment and maintain a high level of customer service? Detailed oriented with good follow-up skills? Proficient in computer usage with standard business software |
| Astellas Pharma, Inc. |
Oklahoma City |
OK |
9/3/2010
|
| Manager, Engineering |
| ? BS in chemical or mechanical engineering or equivalent relevant pharmaceutical science field required. Advanced degree preferred.? A minimum of 5 ? 8 years experience in solid dosage pharmaceutical manufacturing including packaging required.? A minimum two years management of engineers experience required.. ? Additional knowledge in at least one of the following areas is beneficial: Statistical Inference, SPC, Process Capability, DOE, Sampling plan or Risk Assessment.? Must be able to read, write and understand the English language (statement common to all Job Descriptions) ? Must be able to work to meet deadlines, and utilize problem solving skills. Must be able to gather and evaluate complex data to make effective decisions to accomplish work. Strong communication, prioritization and organizational skills. Attention to detail required. Ability to work independently and as a team member. Accurate record keeping.? Minimum supervision required |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Manufacturing Associate II, Bioprocess - Agensys, Santa Monica, CA |
| BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Manufacturing Associate II, Bioprocess -- Agensys, Santa Monica, CA |
| BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Manufacturing Coordinator / Admin, TEMP, Agensys, Santa Monica, CA |
| Qualified candidates shall possess a high school diploma, plus 1-2 years relevant industrial experience related to the manufacture or development of FDA regulated Biological Products. ? Strong knowledge of Access, Excel, PowerPoint and Word a plus? GMP experience is preferred ? Ability to complete tasks with minimal direction from manager and/or supervisor? Must have the ability to prioritize multiple projects/workflow and must manage time efficiently in order to meet established timelines? Highly motivated, strategic thinker, multi-tasking skills, who can effectively drive programs forward in a cross functional team oriented environment. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Marketing Director, Latin America |
| ? 7-10 years of experience? Infectious Disease/Oncology experience.? English/Spanish required. Portuguese desirable.Required Qualifications:1. Bachelor's degree in a related discipline with an advanced degree in business. Science degree preferred. Marketing experience in specific therapeutic area may be required.2. 10+ years of relevant experience depending on degree, including 5 years marketing leadership experience within the Pharmaceutical industry.3. Global and regional marketing experience required preferably in Latin America.4. Requires significant communication and leadership skills and the ability to create and implement the Marketing Plan and integrate it with APLA objectives.5. Strong relationship management and influencing skills and comfort working with cross-functional teams.6. Excellent oral and written communication skills. Ability to understand and help define business questions and present findings in a compelling manner to various audiences.7. Ability to travel domestically and internationally required (up to 50%).8. Fluent in Spanish/English with Portuguese highly desirable. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Director Managed Care Mktg & Alliances |
| Responsible for the development/implementation of managed care marketing strategic and tactical plans for the Health Systems Organization. Requires significant communication and leadership skills and the ability to create and implement the department?s mission and integrate it with that of the company?s. Must have the ability to integrate data/information from various brand teams, account managers, field sales and primary and secondary market research to develop strategies and tactics that enable attainment of assigned outcomes according to the Health System plan. Responsibilities will also include leading cross-functional brand marketing teams to achieve business goals. Job Responsibilities:1.) Lead and manages a cross-functional team which includes multiple brand managers and key stakeholders in the development of the Health Systems Business Plan.2.) Implements strategic and tactical programs to enhance Health Systems perception and brand products in eyes of managed care customers.3.) Lead the creation of pull-through materials for use by field sales to capitalize on managed care victories.4.) Develops and implements managed markets marketing plans and strategic initiatives to achieve business objectives.5.) Manage outside agencies and consultants projects and budgets.6.) Assists in the development of sales training materials required to implement strategic and tactical programs.7.) Manages defined budget for promotional activities as established by Health Systems.Job Requirements:? Four-year college degree in related field or equivalent required (MBA preferred)? 10 years of progressive account management, sales management and marketing experience in Pharmaceutical industry? Demonstrated expert understanding of managed markets and the US healthcare system? Matrix management skills? Proven analytical and quantitative skills ? Strong track record in managing project teams ? Ability to manage expense budgets to optimize returns? Proven oral and written, communication skills? Understanding of the pharmaceutical regulatory environment Additional Skills/Capabilities:? Ability to multi-task? Entrepreneurial in nature? Ability to work on your own? Proficient in power-point / excel |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Assistant Director, Quality Systems |
| Minimum BA / BS or equivalent, advanced degree preferred, with a minimum 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, and commercialization. Ability to contribute to local and global Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region.Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Commercial Products and GMP programs, initiatives and teams, with minimal management oversight. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, Quality Assurance, R&D Programs, GCP |
| Minimum BA / BS or equivalent, science-related preferred, with 10 years of industry experience, 6 years of QA experience, and 3-5 years managing staff.GCP Quality Assurance experience required and experience in a pharmaceutical manufacturing or clinical development environment preferred. Comprehensive knowledge of GCP regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Demonstrated ability to establish local and regional Quality policies and to contribute to global Quality policies in support of the quality system.Ability to assist or lead strategic development and/or successful execution of plans and initiatives that ensure long term success for R&D Programs GCP at a Regional or Global level with minimal management oversight. Demonstrated accountability to resolve complex and diverse problems with decision making responsibility that has a significant impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and across the APGD.Demonstrated ability to anticipate, proactively respond to trends, and/or shifts in the external environment (e.g., regulatory, business partner relationships, industry standards) and to predict impact on quality assurance and/or Astellas business units.Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an ability to interface regionally across multiple departments, and among various levels of management within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. Assist in the identification and implementation of short and long-term business planning strategies, assuring quality is taken into consideration.Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director Quality Assurance - Agensys, Santa Monica, CA |
| 1. Minimum BA/BS degree with 8 years experience in Quality and 4 years managing staff and 10+ years in the pharmaceutical industry. 2. Comprehensive knowledge of GCP , GLP, and GMP and other regulations relating to product development, testing, submission and commercialization.3. Ability to contribute ideas for strategies and tactics to ensure adequate long term planning for the quality assurance function.4. Ability to establish standards in support of the quality system and to interface across multiple departments and levels of management.5. Practical experience of line management position while demonstrating a desire for creative, hands-on approach to leadership in support of a fast growing organization.6. Effective project management skills and commitment to meeting deadlines and work well under pressure.7. Excellent written and oral communication, facilitation and influencing skills with an ability to work within an environment which utilizes both in-house and out-sourced (contract/temporary) resources. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Director, Quality Systems |
| Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10+ years of industry experience, 8 years of QA experience, and 4 ? 6 years managing staff.Experience in managing a Quality System within a GCP / Pharmacovigilance environment. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Establishes local and regional Quality policies in support of the quality system.Effective written and oral communication and interpersonal skills. Influencing skills with a demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change.Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans.Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact within QA and/or with functional groups within the region.Demonstrated experience leading strategic development and successful execution of plans and initiatives for addressing complex and diverse QA matters with minimal management oversight. Contributes to the identification and implementation of long-term business planning strategies, assuring quality is taken into consideration. Demonstrated ability to develop quality assurance professionals to both lead and manage a functional quality assurance unit.Demonstrated experience in hosting and facilitating regulatory agency inspections with successful outcomes. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, Regulatory Affairs |
| KNOWLEDGE & EXPERIENCE: ? Bachelor?s degree in scientific discipline; advanced degree preferred.? 9 years previous pharmaceutical drug development experience, 2 in managing staff.? Recognized as an expert in regulatory aspects of pharmaceutical drug development involving undefined frameworks with technical complexity and broad scope.? Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development. Recognized as an expert in an aspect of pharmaceutical drug development. ? 6 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA and ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submissions and negotiations with the FDA in areas of CMC and product formulations. Regulatory experience in other therapeutic areas such as medical devices or biologics.? Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to direct reports and others in the department as needed.? Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.? Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence department staff and other APGD groups.? High integrity with respect to maintenance of proprietary, confidential information. ? Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director / Senior Director, Discovery - Agensys, Santa Monica, CA |
| ? Advanced degree (Ph.D., or equivalent) with at least 10 years? experience in an industry setting in Drug Discovery and related areas with an emphasis on target discovery and validation, and monoclonal antibody discovery and engineering. ? Strong background in Oncology drug discovery, evidenced by involvement in development of product candidates from initiation to clinical stage, some experience with biologics is preferred.? Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals.? Demonstrated successful program leadership and multi-project coordination. ? At least 5 years of management experience of multiple groups. ? Proven track record in leading programs to achieve goals and timelines.? Ability to perform successfully in a cross-functional team environment.? Excellent written and verbal communication skills. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| : Associate/Sr. Associate, Cell Line Development, Agensys, Santa Monica, CA |
| ? The ideal candidates will have a B.S. or M.S. in Biology, Molecular Biology, Biochemical Engineering,or related field, with preferably a minimum of 2 years of relevant experience in industry.? Experience in generation of transient/stable cell lines and mammalian cell culture are required.? Working knowledge of antibody expression and detection in mammalian cells is preferred.? Compliance with appropriate written procedures; e.g. applicable safety, biological containment, and administrative procedures is required. ? Excellent written and oral communication skills and the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Analytical Associate/Sr. Analytical Associate, Process Development - Agensys, Santa Monica, CA |
| The successful candidate will possess the following qualifications.? B.S. or M.S. in biochemistry, chemistry, or related field with at least three-year experience inbiotechnology/biopharmaceutical industry.? Experience in protein analysis by HPLC, gel electrophoresis, UV/Vis spectroscopy, and plate-basedprotein assays such as BCA and ELISA. Experience in CE and DSC is a plus |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Biostatistics Director, Oncology |
| M.S. or Ph.D. in statistics or equivalentRequired proven oncology experience Minimum of 8 years experience in applying statistical methods in biomedical research, extensive pharmaceutical or CRO experience requiredExperience in working on clinical project teams. Good understanding of entire drug development process - ability to see the ?big picture?.Experience as the independent lead statistician in a regulatory submission preferredExperience with cross functional process improvement or innovation initiativesAdvanced and broad knowledge of statistical methods, along with understanding of industry practices related to the statistical analysis of clinical dataKnowledge and skills in SAS required and knowledge of other statistical software preferred.In-depth familiarity with processes and procedures in data management and SAS programmingExperience working in an international environment and demonstrated ability to manage and influence across different locations, time zones and cultures; builds global relationships. Ability to work in a matrix environment. Proven excellent organizational, project and time management skills.Leadership skills and ability to delegate appropriately and provide direction to more junior Biostatisticians. Very good oral, written, and presentation communication skills. Able to clearly communicate statistical issues and methods to both statisticians and non-statisticians. Very good problem solving skills.Accurate with a keen eye for detail. Dedication to quality and reliability in all work tasksAbility to perform under pressure |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director / Director Statistics |
| MS or PhD in statistics or mathematics; minimum of 7-10 years in pharma or CRO industry, with minimum of 2-4 years in functional or project management roleAt least 2 years experience in working on global clinical studies and projects or global process and system initiativesVery good understanding of all phases of clinical development, and processes in data scienceExperience in all aspects of statistics for clinical trials, and in working as a member of a project team including design of clinical studies and contribution to Clinical Development PlansExperience as lead statistician for multiple submissions to health authorities, substantial experience in interations with health authoritiesGood understanding of the various functions and expert groups contributing to Drug Development Solid knowledge of SAS and other statistical toolsMinimum requirements for Director level:Generally a minimum of 10 years of relevant experience in pharma or CRO industryMinimum of 4-5 years of management experience including 2-3 years in a line management positionDemonstrated ability to translate strategic plan for GDO, Data Science and Statistics into goals and objectives for own functionDemonstrated leadership skills and ability to effectively prioritize own group?s activities for development projects and clinical trialsProven ability to establish operating guidelines and procedures, preferably in a global settingDemonstrated ability to successfully identify and lead global process or system improvement initiatives |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Associate Director, Clinical Pharmacology - Agensys, Santa Monica, CA |
| ? PhD, PharmD, MS, BS in Pharmacy or life sciences with extensive training in pharmacology, pharmacokinetics, and pharmacodynamics and data analysis -- also beneficial to have experience with population PK/PD modeling and simulation? 8-10 years of Phase I clinical trial experience or equivalent? 5 years of experience with oncology drug development? 5 years of experience with antibodies ? Knowledge of global drug development process and ability to design and implement development plans? Extensive experience in representing Clinical Pharmacology to regulatory agencies ? Established leadership skills? Proven communication, management and leadership skills |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Director, CPED Science, Oncology |
| Minimum MS or equivalent qualification in a bio-medical/science field required. MD or PhD desired.The Assistant/Associate Director role requires at least 5-7 years post-graduate experience, in pharmaceutical industry, preferably from another (major) Pharma Company with a general understanding of Drug Discovery and Development. In addition, the individual should have the following experiences.Expert knowledge of disease biology and relevant clinical disease knowledge required to design early development strategies up to and including PoC.Expert knowledge of Clinical Pharmacology Knowledge and proven development expertise in at least 3 therapeutic areas.Team player with strong written and communication skills to bring over and get acceptance for plans.Strong, critical analytical mindOperate with minimum of supervision.Key organizer and planner who clearly sets priorities.Up to date with latest ICH-GCP guidelines and other relevant regulations.Highly developed sense for ethical conduct of Clinical Development |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Associate Director, Quality Assurance - Agensys, Santa Monica, CA |
| 1. Minimum BA / BS or equivalent, advanced degree preferred, with a minimum of 10 years of industry experience, 6 years of QA experience, and 3 - 5 years managing staff. 2. Comprehensive knowledge of GxP and other regulations and understanding of global quality standards relating to product development, submission and/or commercialization. Ability to contribute to local and global Quality policies in support of the quality system. 3. Effective written and oral communication and interpersonal skills, facilitation, and influencing skills with an demonstrated ability to lead projects, initiatives, or programs across multiple departments, regions and business units within Astellas group and external stakeholders. Demonstrated ability to solicit input and liaise with stakeholders to prioritize and set strategic direction for change. 4. Demonstrated ability to assess the state of current business and QA operations for Quality Systems to identify and recommend future state, improvements, and to implement action plans. 5. Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact (e.g., stakeholder relationships, dossier approvals, compliance status, credibility and/or revenue) within QA and within the region. 6. Demonstrated experience developing quality strategies and priorities and translating them into short and long-term objectives for the department. Ability to provide leadership to Quality Systems programs, initiatives and teams, with minimal management oversight. 7. Demonstrated ability to develop quality assurance professionals and to both lead and manage a functional quality assurance unit. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Associate Manager, Outsourcing |
| Bachelors Degree in Business, Life Sciences or equivalent experience, Master?s Degree or other Advanced degree preferred.Generally 7 + years experience required in R&D Outsourcing, Clinical or Business Operations within a pharmaceutical company required.Strong analytical and problem solving skills and ability to come up with creative solutions.Strong team player.Demonstrated negotiation and influencing skills.Demonstrated ability to provide leadership.Demonstrated ability to strategically manage vendor relationships.Demonstrated ability to manage multiple projects simultaneously.Demonstrated ability to effectively communicate across all levels of management. Advanced use of word processing and spreadsheet software. Strong written and oral communications skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Associate Medical Director, Oncology - Agensys, Santa Monica, CA |
| M.D. degree, Board Certified or Board Eligible in OncologyMinimum two years of experience in both laboratory or clinical research and pharmaceutical industry.Strong working-knowledge of regulatory procedures and guidelines (preferably US)Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Asst. Animal Technician/Animal Technician/Sr. Animal Technician - Agensys, Santa Monica, CA |
| Previous husbandry experience of laboratory rodents is highly desirableAn ALAT or higher certification and understanding of AAALAC accreditation are a plus. A BA/BS degree is a definite plusThe successful candidate must follow all animal health standards, stringent SOP?s and safety protocols, be able to lift objects of approximately 50 pounds and should have no allergies to common laboratory rodentsThe incumbent should have a general appreciation for biological science and an understanding of the intricacies of laboratory research.This person should have good verbal and written communication skills and the ability to work well in a team environment with a positive/can-do attitude.The person should also be detail-oriented and willing to work flexible hours. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director, in vivo Pharmacology - Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Director, Translational Research - Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D./M.D. with a minimum of 10 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing scientists is required. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Director/Senior Director, Global Development Project Lead, Oncology |
| An MD, PhD or PharmD is preferable with a specialty in the assigned oncology area, or equivalent experience with global development required. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Global Development Project Leader - Central Nervous System |
| An MD, PhD or PharmD is preferable with a specialty in the CNS therapeutic area required along with experience in global development. Experience in the area of Alzheimer disease preferred. Total leadership experience including line/project management. multidisciplinary program management experience, which includes leadership in more than one IND/IMPD, NDA/MAA, Advisory Committee or other PMDA/EMEA/FDA meetings.Minimum of ten (10) years experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology.Demonstrated experience leading the development of at least one development candidate with adherence to quality, excellence and efficiency.Demonstrated experience leading drug development projects and activities in a matrixed, global organization. A broad understanding of how to communicate and work well with team members and relevant people as well as scientists and external decision-makers worldwide. A thorough understanding of how to influence local and global regulatory, scientific and commercial environments.Skill Set:o Ability to assimilate data, recognize key variables and analyze complex situations. Make quality judgments.o Has a realistic expectation of the business, one?s self and others.o A style which builds alliances within the organization, locally/globally, and/or corporate collaborators.o Does not confuse effort for results.o Tenacity to weather short-term setbacks for long-term advantages.o Broad understanding of the multidisciplinary functions contributing to effective and efficient drug development.Solid understanding of CMC, pharmacology, toxicology, PK, clinical requirements to support major regulatory filings ? IND/IMPD, NDA/MAA.Leads preparation of PMDA/EMEA/FDA milestone meetings, such as Pre-IND, End-of-Phase II, Pre-NDA, Advisory Committees, focusing on the key strategic issues.Excellent understanding of the interdependencies of the various disciplines (CMC, Pharm/Tox, PK, Clinical, Regulatory, Marketing, Finance, etc) - what needs to be evaluated simultaneously vs. sequentially etc. from a strategic planning/risk management time/event/cost point locally and globally.Understanding of how to educate/advise others on Regulatory Guidances/Internal SOPs/PM concepts. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Laboratory Manager - Agensys, Santa Monica, CA |
| EDUCATION: B.S./M.S. degree in Science.Experience: At least five years of Lab management experienceThe successful candidate must demonstrate a strong working knowledge of pharmaceutical/biotechnology research laboratories and their unique safety issues, including vivarium facilities and familiarity with IACUC regulations. Experience in industry is strongly preferred. Strong written and verbal communication skills, as well as interpersonal skills are also essential. In addition, the successful candidate must have the ability to demonstrate leadership and problem solving skills in a team based environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Manager/Senior Manager CMC Analytical Development - Agensys, Santa Monica, CA |
| PhD in chemistry, biochemistry or biology with 10+ years experience in development, qualification, and transfer of chromatographic, spectrophotometric, electrophoretic, and other relevant analytical methods for protein biotherapeutics in a biopharmaceutical environment. -hands-on experience and a good understanding of LC-MS and MS/MS for biologics is a must; the ability to troubleshoot complex technical and scientific problems; an in-depth understanding of protein characterization techniques: proven supervisory and managerial skills are essential; -a high level of expertise with cGMP, and regulatory compliance in biotechnology product development is expected; -experience with immunological methods is a strong plus; experience with analytical test method development for small molecular is preferable. Must be able to perform in a fast paced multiproduct environment. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Medical Director, Medical Sciences- Oncology |
| M.D. degree, Board Certified or Board Eligible in Oncology/Hematology.Minimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Knowledge of regulatory procedures and guidelines (preferably global)Experience in clinical development, preferably experience in at least 2 phases Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Medical Director, Product Safety & Pharmacovigilance |
| This position is responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations. Additionally responsible for strategies in monitoring and analysis of cumulative safety information on Astellas products. Responsible for drug safety crisis managementSpecific responsibilities include:Guides regulatory reporting including individual case safety reports (ICSRs), NDA annual report summary statements, and Periodic Safety Update Reports (PSURs)Guides adverse event coding, retrieval and analysis activities in drug safety and clinical trialsGuides reviews of safety sections of NDA submissionsPlans cumulative safety information analysis such as signal detection from company or public databases with data miningGuides safety updates of company core data sheet and local product labelsGuides pharmacoepidemiology projectsGuides crisis management on drug safetyGuides Risk Management Plans for specific productsGuides and coordinates preparation of ad-hoc benefit-risk assessment documentsGuides regulatory strategy and preparation of data related safety to regulatory authorities and advisory committeesInterfaces with Medical Sciences, Clinical Studies, Product Safety Management, Drug Development and Project Management, Pharmacoepidemiology, Global Pharmacovigilance departments, Toxicologist, Biopharmaceutical sciences, Research Data Sciences, Legal Demonstrated leadership skills and strategic focus. Demonstrated ability to exercise independent judgment and effectively collaborate with multiple functional unitsPosition requirements: MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Medical Director/Senior Medical Director, Oncology |
| M.D. degree or equivalent; Board Certified or Board Eligible in oncology highly desirableMinimum 6 or more years experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably global)Experience in P1-3 clinical development; prior EU/US regulatory filing experience expected.Holds others accountableStrong industry acumen, vision and perspective |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Medical/Senior Medical Director, Pharmacovigilance- Oncology |
| SUPERVISORY RESPONSIBILITY: Directly supervises Assistant Medical Director(s), Associate Medical Director(s), and/or Medical Director(s) in the PSP Department.KNOWLEDGE & EXPERIENCE: Identify specialized knowledge needed to perform the position. The years of experience are not required. Note if the specific knowledge or skill is required, desirable, or a plus.MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| PET Senior Research Associate- Agensys, Santa Monica, CA |
| This position requires a Bachelor/Master?s Degree of Science and at least three years of direct animal research experience utilizing microPET/CT systems; an associates degree and Five years animal research experience with at least 3 years utilizing PET/CT; or eight years directly related animal research experience with 5 years utilizing PET/CT .AALAS certification at the LATG level is also required. The qualified individual must possess excellent organizational and communication skills, exhibit problem solving skills, as well as a desire to learn new techniques and train others in a team environment. This role also requires the individual to be "results-driven" with the ability to think through processes in order to improve efficiency and outcome of studies required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Project Management Specialist - Agensys, Santa Monica, CA |
| The ideal candidate will have a university degree and a minimum of 5 ? 8 years related experience in Project Management or in Drug Development ? preferably both. Even more preferable would be Drug development project management experience in biologics or biologic-based drugs. Working knowledge of PM tools such as MS Project and MS Excel is required. Experience in initiating and implementing additional communication, planning, scheduling and development strategy software tools are a plus. Excellent communication skills and the ability to work in a team environment are essential. PMP certification a plus but not essential |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Project Manager/Senior Project Manager, DDPM |
| Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, five (5) years with Masters Degree or seven plus (7+) years relevant experience with a minimum of three to five (3-5) years experience directly related to drug development process with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| QA Associate I - Agensys, Santa Monica, CA |
| ? Minimum 3-5 years GMP experience required? BA or BS Degree in Life Sciences or 5-7 years of professional GMP experience? Previous Quality Assurance signature approval of controlled documents required? Strong computer skills recommended, experience with Access / Trackwise highly desirable? Strong oral and written communication skills required? Experience reviewing, creating, and implementing Standard Operating Procedures preferred? Experience with equipment validations preferred |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| QA Document Specialist - Agensys, Santa Monica, CA |
| ? 2-5 years in cGMP experience preferred? BA or BS Degree in Life Sciences preferred? Proficient computer skills in Microsoft Word, Excel, and PowerPoint. MS Access experience is a plus.? Quality Assurance controlled document experience recommended.? Detail oriented and able to work effectively independent of direct daily supervision? Strong oral and written communication skills required? Flexible and fast learning team player. ? Organized and able to multi-task in a fast-paced environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Quality Control Microbiologist - Agensys, Santa Monica, CA |
| ? A Bachelor?s degree or equivalent work experience in microbiology or science discipline. Must have 1 ? 2 years experience in a GMP Microbiology pharmaceutical or biopharmaceutical environment. Familiarity with cGMP manufacturing a plus.? Must have strong teamwork and organizational skills ? Resourceful, self-reliant, self-motivated, and confident ? Excellent verbal and written communication skills ? The ability to multitask and exercise good judgment ? Detailed oriented with good follow-up skills ? Assist with administrative tasks related to the department ? Maintains good aseptic technique, housekeeping, order, and safety in the laboratory? Maintain logbooks, record and report all test results in a timely manner ? Revise procedures as necessary to improve efficiency and ensure compliance with regulatory requirements ? Must be familiar with Microsoft Word and Excel |
| Astellas Pharma, Inc. |
Skokie |
IL |
9/3/2010
|
| Research & Development Future Opportunities |
| ? Positions in the Research & Development division at Astellas require degrees in science; advanced degrees plus industry experience are preferred. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate /Senior Research Associate in vivo validation, Agensys - Santa Monica, CA |
| The ideal candidate should have a bachelor or master degree in biological sciences with a minimum of 2 years of related research experience after graduation, preferably in an industry setting. Previous experiences in handling research rodents, especially immunodeficient mice in oncology research and human cancer cell culture are absolutely required. Experiences in pre-clinical validation of cancer therapeutics using human tumor xenograft models, microsurgical procedures in laboratory rodents, human tumor xenograft characterization and human cancer primary cell line establishment are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate, Protein Science - Agensys, Santa Monica, CA |
| Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 2 years of laboratory experience. Industrial experience protein analysis and protein purification is highly preferred. Experience in proteomic method development and hands on experience with Biacore are also preferred. The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/ Senior Research Associate ? Molecular Biology - Agensys, Santa Monica, CA |
| The ideal candidate will have M.S. (preferred) or B.S. in Molecular Biology or related field, with a minimum of five (5) years of relevant research experience. Experience in molecular biology techniques and methods, with emphasis on gene expression and gene structure analysis is required. The ability to reliably handle and process precious and limited specimens is essential. Excellent verbal and written communication skills, as well as the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/Senior Research Associate: Antibody Drug Discovery - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Industrial experience is preferred. Excellent verbal and communication skills and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Quality Assurance Associate - Agensys, Santa Monica, CA |
| ? PhD in Life Sciences preferred.? Minimum 2 years in a pharmaceutical development environment with solid knowledge and review experience of in-vivo and in-vitro study protocols and reports. Additional quality assurance experience in a research environment with programs such as document management and equipment qualification is recommended.? In-depth understanding of pre-clinical pharmacology studies. ? Strong oral and written communication skills are required.? Strong interpersonal skills and the ability to work in a project team environment are a requirement. ? Fluency with Word, Excel, and Access databases is recommended. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Research Scientist, Pharmacology - Agensys - Santa Monica, CA |
| Candidate consideration requires a Ph.D., or an equivalent degree, in Biology, Pharmacology, Immunology, Biochemistry or a related field with a minimum of 3 years of post-doctoral experience. Previous hand-on experience using human tumor xenograft models in oncology research, as evidenced by publications, is required. Understanding the basic concepts of pharmacokinetics and pharmacodynamics and be able to analyze relevant data are highly desired. Experience in human tumor xenograft and primary cell line development is a definite plus. Previous experience in preclinical evaluation of cancer therapeutics using xenograft models preferably in an industry drug discovery setting and experience managing research associates are preferred. Successful candidates should have strong written and oral communication skills, be self-motivated and able to demonstrate leadership. Developmental opportunities include leading research projects and building new technology platforms. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Safety Scientist/Principal Safety Scientist, Oncology |
| Minimum of Bachelor?s Degree in Science or Pharmacy or Nursing required.Minimum of 5 years pharmaceutical experience in a clinical safety/research department required.Minimum of 5 years of medical writing experience (Prefer experience in writing pharmaceutical reports such as Clinical Study Reports, Safety sections of the ISS and/or EU Common Technical document, PSUR or white paper).Proven ability to critically evaluate medical data.Proven understanding of clinical disease state and implications of treatment.Proven ability to communicate effectively (verbal, presentation at group meetings, etc).Proven experience with project management (formal or informal).Prefer experience in training or mentoring.Strategic thinking, Organizational, Leadership, Results-oriented performance, Team player.Excellent knowledge of ICH, US & EU regulations and requirements for pharmacovigilance (experience with world-wide safety reporting regulations and guidelines required).Excellent interpersonal skills, including ability to work effectively cross culturally and cross functionally.Proven ability to effectively lead cross-functional teams with respect to risk management activities and to influence where direct reporting line relationships do not exist. Excellent written and spoken English |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Scientist, Process Development in Antibody Drug Conjugates - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemistry, Chemical Engineering, and Biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of organic synthesis processes. ? Direct experience in protein purification, conjugation of monoclonal antibodies to small molecules, and process scale-up. ? Experience with HPLC, LC/MS-ESI, chromatographic techniques and immunologic assays including ELISA and immunoblotting? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation, chromatography, UF/DF, and filtration? Supervisory experience and experience with coordinating activities with CMOs are preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Scientist/Senior Scientist, Antibody Drug Conjugates, Drug Discovery - Agensys, Santa Monica, CA |
| PhD in biological sciences, with 5+ years of relevant industrial experiencePrevious background with chemotherapeutic drugs, monoclonal antibodies and/or antibody drug conjugates for oncology with some in vivo tumor biology experience is highly preferred.Excellent analytical, oral and written communication skills and a demonstrated ability to operate both independently and in a team environment.Strong data analytical skills, excellent communication and supervisory skills are required.The qualified candidate should be a highly motivated, strategic thinker with excellent organizational skills who can effectively drive programs forward in a cross functional team oriented environment. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Clinical Study Management |
| Minimally a BS. Must have at least 10 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of Clinical Study Managers in multiple therapeutic and geographic areas. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other development functions in the development and support of medicines. Must have an in-depth personal experience and understanding of the Clinical Science function and the critical contribution of Clinical Operations to drug development, Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments globally and on a multi-country and regional level, in site and patient recruitment, site monitoring, essential document collection and management, and the optimal use of cross functional outsourcing relationships. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Global PK Modeling & Simulation |
| PhD in Life Sciences required. Must have at least 10 or more years of pharmaceutical industry experience, specifically in global human drug development, both in exploratory development, late clinical pharmacology and later phases of development. Broad therapeutic area knowledge and prior experience with biologicals is important. Extensive knowledge experience in application of PKMS in global drug development, both in Exploratory Development as wel as late CP. Good understanding of Late Development as well as Drug Discovery.Good knowledge of mathematics and power of mathematical modelsMust have a successful track record in interactions with Global Regulatory authorities; prior experience contributing to successful regulatory filings highly important. Must have a successful track record in the hiring and retention of excellent scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GCPED, APGD and Astellas.Must have an in-depth personal experience and understanding of the GCPED function and its critical contribution to drug development. Must have extensive experience in interactions with global Regulatory Authorities. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments as it relates to GCPED and Astellas business. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 1-3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Director, Statistics & Clinical Programming |
| Minimally a PhD in Statistics, or equivalent Degree, with specialization in Pharmaceutical Drug Development or equivalent work experience. Must have at least 10-15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers within a biometrics, biostatics function in clinical development. Preferably, will have successfully led a global Biostatistics and Programming function in a major pharmaceutical company. Must have a successful track record in the hiring and retention of excellent statistical and data management scientists who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. Must have an in-depth personal experience and understanding of the relevant expert groups within the Statistics and Programming function and their critical contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments in the area of design, acquisition and reporting of data in the pharmaceutical industry. Must have extensive knowledge of the application of statistical analysis and reporting tools. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction.Displays the highest level of personal commitment to the Astellas code of Ethics. Is exemplary in ensuring that "every employee deserves a great manager". Inspires while holds all appropriately accountable. Commits through co-accountability, to the growth and health of GDO, APGD and Astellas. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Medical Writing Program Manager, Oncology |
| BA/BS degree or equivalent; 10+ years relevant experience. Preferred: MS/MA/MPH with at least 7 years as a writing professional in pharmaceutical industry.Activities require expert technical skill (e.g., as defined by Drug Information Association Medical Writing Competency Model) including techniques of scientific writing and editing; ability to interpret and communicate clinical and numerical data, and verify consistency in data; comprehend and communicate scientific concepts; interpret and communicate clinical, nonclinical, biopharmaceutic, pharmacology, ADME and CMC data and information.Activities require advanced document and process experience, and highly complex problem solving/issue resolution to achieve corporate objective(s), resourcefulness and sharing of expertise.Technical expert for the majority of document types produced by medical writing. Demonstrated and substantial experience in managing the creation of IND/IMPD or NDA/MAA components, briefing documents and white papers. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Senior Project Manager, DDPM |
| Bachelors Degree required. Advanced degree (masters, doctorate) a plus. Generally, seven (7) years with Masters Degree or ten plus (10+) years relevant experience with a minimum five to seven (5-7) years experience with a demonstrated understanding of the drug development process, and project management skills required. Knowledge of required CMC, pharmacology, toxicology, PK, clinical requirements to support major US regulatory filings ? IND, NDA, etc.Demonstrates clear depth and breadth of understanding of critical early drug development processes Demonstrated expertise /discipline in project management and a key organizer who has shown to set clear priorities on developmental activities, with experience in planning systems (e.g. MSProject) and an understanding of financial planning / expenditures. Good communication, people management and social skills with a good sense of diplomacy both in a scientific and industrial environment.Effectively utilizes information technology systems and provisional project management tools.Capable of managing meetings within a multicultural environment and organize expert meetings with KOLs. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Research Associate, Protein Mass Spectrometry- Agensys, Santa Monica, CA |
| Candidate consideration requires a B.S. or M.S. in chemistry, biochemistry or similar field with a minimum of 7 years of laboratory experience. Industrial or academic experience in protein and proteomic analysis by advanced mass spectrometry methods is highly preferred.Hands on experience in protein mass spectrometry method development and experience with Thermo LTQ line of instruments as well as using computational methods for MS data processing are also preferred.The successful candidate will have strong written and oral communication skills, be self-motivated, possess strong organizational skills, and have a track record of working successfully in a team environment. |
| Astellas Pharma, Inc. |
Skokie |
IL |
9/3/2010
|
| Senior Scientist, Bioanalytical Laboratory - Pharmacodynamics |
| Ph.D. in molecular or cellular biology (or equivalent) with 3+ years of related industry experiences, or M.Sc. in science (major in molecular or biological sciences) with 5+ years of related industry experienceKnowledge and experience in molecular/ PCR-based testingKnowledge and experience with immunoassaysKnowledge and experience in biological sample preparationsKnowledge of FDA guideline for bioanalytical method validationWorking knowledge of SOPs and GLP regulatory guidance Ability to transfer and validate biomarkers, immunogenicity and immunoassay methods Knowledge of computer software for laboratory data management Skills in conducting bioanalytical research especially for running clinical samples, documenting data, and assisting report writing following the regulatory requirements.Self-motivated, excellent team player with good communication skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Senior Scientist/Group Leader, Antibody Generation and Production - Agensys, Santa Monica, CA |
| Ph.D. or equivalent in Immunology, Biochemistry or a related discipline, with at least 8 -10 years of demonstrated experience in a relevant field working either in an academic or bio-pharmaceutical environment. The qualified candidate will have broad experience and knowledge in all aspects of hybridoma or recombinant antibody technologies, including phage display; will be an accomplished investigator with a solid publication or patenting record. Finally the successful individual must be a self-starter, with excellent managerial, communication and interpersonal skills. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Sr. Director, Global Business Information Management |
| Minimally a BS. Must have 10- 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing a BISM Function globally. Must have a successful track record in the hiring and retention of excellent business interface resources who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, in the development and support of medicines through optimal use of relevant technologies. Must have an in-depth personal experience and understanding of the BISM function, current and future technologies needs and investment and their critical contribution to GDO's successful contribution to drug development. Must also have an understanding of the functions of multiple business units throughout the company, and have maintained effective collaborations with leadership of those business units and functions. Is considered an industry expert and is able to recognize the implications of new directions, trends and developments. Must be a strong and effective strategic thinker and problem solver, requiring the ability to both recognize and anticipate problems, and also help managers and individuals develop their own problem solving skills and discipline. However, must also be able to identify and solve tactical problems and delve into high degree of detail when necessary. Plans for and has detailed knowledge of all available resources internally and externally, has developed the appropriate relationships with partners and vendors, and has the ability to marshal those resources in a productive and efficient manner, either as part of a 3 year strategic capacity plan, or when there is need for sudden and immediate change in direction. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
9/3/2010
|
| Sr. Scientist/Scientist, Cell Culture Process Development - Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Chemical Engineering, Biochemical Engineering or biology) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Knowledge of the design, optimization and scale-up of cell culture processes is a necessity. Direct experience with mammalian cell culture process development and process transfer for clinical or commercial manufacturing of biopharmaceutical product(s) highly preferred.? Knowledge in the use of DOE to conduct experiments? Hands-on experience with unit operations such as lab and pilot-scale bioreactor operation,centrifugation, clarification, and filtration.? Process validation and cGMP experience is desirable.? Supervisory experience preferred.? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Vice President, Global Clinical Science |
| Minimally a BS Degree. Must have at least 15 years of pharmaceutical industry experience specifically in human drug development, and at least 3-5 years managing managers of multiple groups within the area of Clinical Operations/Clinical Science. Previous experience in leading a Global Clinical Operations function is preferable. Must have a successful track record in the hiring and retention of excellent clinical operations resources globally, who work optimally in a cross functional team and matrix environment. Must have a successful track record in effectively collaborating with other functions in development, discovery research, Medical Affairs and Commercial in the development and support of medicines. |
| Astellas Pharma, Inc. |
Seattle North (5PP50406) |
WA |
9/3/2010
|
| Executive Representative Hospital- Seattle, WA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Freehold |
NJ |
9/3/2010
|
| Executive Representative, Hospital - Central NJ |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Manhattan (South) |
NY |
9/3/2010
|
| Executive Representative, Hospital - Manhattan (South), NY |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is required |
| Astellas Pharma, Inc. |
Harrisburg (2A020506) |
PA |
9/3/2010
|
| Executive Representative, Hospital- Harrisburg, PA |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
San Francisco (5AA50505) |
CA |
9/3/2010
|
| Executive Representative, Hospital- San Francisco, CA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Philadelphia North (1P010604) |
PA |
9/3/2010
|
| Professional Representative PCP - Philadelphia North, PA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Bridgeport (1P010207) |
CT |
9/3/2010
|
| Professional Representative PCP- Bridgeport, CT |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Jersey City (1V010400) |
NJ |
9/3/2010
|
| Regional Sales Manager - Specialty; Jersey City, NJ |
| Job Requirements:- Valid driver's license - Minimum of 5-7 years experience in pharmaceutical sales or related fields, including primary care and specialty sales (preferably hospital sales experience) . - Prior experience in managing field representatives is preferred - Must provide evidence of leadership skills and successful contributions outside immediate team (i.e., training, mentoring, process development, etc.) - A demonstrated high degree of proficiency in managing multiple projects - Proven presentation, coaching, and teaching skills. - Demonstrated ability to consistently meet and exceed sales quota goals - Proficient with basic computer skills. - 4 year college degree |
| Astellas Pharma, Inc. |
Seattle North (1V060202) |
WA |
9/3/2010
|
| Senior Professional Representative II, Specialty - Seattle North |
| REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree |
| Astellas Pharma, Inc. |
WI (5DC40205) |
Milwaukee |
9/3/2010
|
| Sr Executive Representative Hospital- Milwaukee, WI |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Phoenix North (5PP50602) |
AZ |
9/3/2010
|
| Sr Executive Representative Hospital- Phoenix North, AZ |
| REQUIREMENTS:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, Anti-Infective or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Leesburg (1P030304) |
FL |
9/3/2010
|
| Sr Professional Representative PCP- Leesburg, FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Bowling Green (1P050205) |
KY |
9/3/2010
|
| Sr Professional Representative- Bowling Green, KY |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Pharmaceutical sales experience highly preferred- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Colorado Springs (1P060106) |
CO |
9/3/2010
|
| Sr Professional Representative PCP- Colorado Springs, CO |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Decatur (1P030504) |
GA |
9/3/2010
|
| Sr Professional Representative PCP- Decatur, GA |
| - A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Harrisburg (1P010609) |
PA |
9/3/2010
|
| Sr Professional Representative PCP- Harrisburg, PA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Las Vegas East (1P060208) |
NV |
9/3/2010
|
| Sr Professional Representative PCP- Las Vegas East, NV |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Palm Springs (1P060301) |
CA |
9/3/2010
|
| Sr Professional Representative PCP- Palm Springs, CA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
San Jose (1P060507) |
CA |
9/3/2010
|
| Sr Professional Representative PCP- Walnut Creek, CA |
| - A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year minimum) with business-to-business sales-Pharmaceutical sales experience highly preferredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Yonkers (1P010208) |
NY |
9/3/2010
|
| Sr Professional Representative PCP- Yonkers, NY |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Jacksonville (1P030205) |
FL |
9/3/2010
|
| Sr Professional Representative, PCP - Jacksonville (South), FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Extensive travel is required for this position- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Jacksonville (5DA20405) |
FL |
9/3/2010
|
| Sr. Executive Representative, Hospital - Jacksonville, FL |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Washington - East (5DC10403) |
DC |
9/3/2010
|
| Sr. Executive Representative, Hospital - Washington, DC (East) |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Astellas Pharma, Inc. |
Sacramento (1V060207) |
CA |
9/3/2010
|
| Sr. Professional Representative , Specialty - Sacramento, CA |
| REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree |
| Astellas Pharma, Inc. |
Phoenix |
AZ |
9/3/2010
|
| Sales Director PCP & Specialty- West Coast |
| REQUIREMENTS:- 8+ years pharmaceutical sales and sales 6 years pharmaceutical sales management experience, some of which needs to be at the director level. - Extensive knowledge of sales processes and pharmaceutical products and industry- Excellent communication, facilitation and presentation skills- Can do approach and excellent motivational and persuasion skills- Leadership skills commensurate with the position- BA/BS degree is required - Extensive travel is required for this position |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Director Medical Affairs, Latin America |
| A minimum of five (5) years in a Medical Director Role.- Medical Degree; must have a License of Medical Doctor & Board certification in at least one specialty with basic medical science and research experience. Experience focused on oncology or immunology preferred. - Strong people management skills- Basic marketing skills as well as understanding business practices and technical terms in business. - Business acumen, a bottom-line orientation, strong management and leadership skills. - Must have proficiency in both Spanish and English (Portuguese a plus) in order to interact with the other team clinicians at the corporate headquarters in the US, as well worldwide. - Present, discuss, negotiate & persuade the global team in English- Self motivated, both strategic and tactical in his/her thought process and capable of becoming rapidly engaged in the company?s business- High degree of self-direction, with the ability to quickly make decisions and accept responsibility for outcomes |
| Astellas Pharma, Inc. |
Deerfield |
IL |
9/3/2010
|
| Manager/Sr. Manager, Supply Chain |
| Minimum 7 years Supply Chain experience required. Experience within the Life Sciences field and an international supply chain background is highly preferred.Bachelor of Science or equivalent required - preferably in supply chain, operations or related discipline. MBA preferred.SAP or other ERP software experience and strong knowledge of Microsoft Office suite required.Has strong understanding of supply chain and manufacturing environments.Possesses strong cross-functional leadership capability.Succeeds at influencing a wide spectrum of stakeholders. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
9/3/2010
|
| Associate Director of Clinical QA |
| Education/Experience
â?¢ Bachelorâ??s or Masterâ??s degree in biology, chemistry or related field
â?¢ Approximately 8-10 years experience in quality assurance with demonstrated expertise in Good Clinical Practice regulations and guidelines
â?¢ Experience with supervision of quality assurance professionals
Knowledge, Skills and Abilities
â?¢ Excellent written and oral communication skills
â?¢ Experience working with external contractors and consultants
â?¢ Strong planning and task management skills
â?¢ Proficiency with Microsoft Office applications
This position is based in IPMâ??s Paarl, South Africa office. Job holder should expect a fast-paced working environment. At least 30% local and international travel will be required. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
9/3/2010
|
| Clinical Regulatory Officer |
| To perform this job successfully, an individual must be able to perform each essential duty satisfactorily:
EDUCATION AND EXPERIENCE
â?¢Bachelorâ??s degree in life science or healthcare field, or equivalent.
â?¢Minimum of 3 years clinical research experience.
â?¢Minimum 2 yearâ??s experience with preparation of clinical trial submissions.
â?¢Previous GCP certification is an advantage.
â?¢Familiarity with Regulatory Agencies in Africa research settings is desirable.
â?¢Valid driversâ?? license.
KNOWLEDGE, SKILLS AND ABILITIES
â?¢Ability to organize and prioritize multiple projects and tasks.
â?¢English verbal and written skills are required.
â?¢Ability to work independently and in a cross-functional team environment.
â?¢Attention to detail and timelines is critical.
â?¢Good understanding of document management.
â?¢Understanding of stakeholder management is an advantage.
â?¢Good conflict resolution and problem solving skills.
â?¢End-user computer efficiency, with proficiency in Microsoft Office products.
Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. A valid driverâ??s license as well as own reliable transport is required.IPM is an Equal Employment Opportunity employer.This job description should not be construed to imply that these requirements are the only standards for the position. Other duties will be assigned. IPM has the right to revise this job description at any time. IPM is an â??at willâ? employer and as such, neither this job description nor your signature constitutes any form of contractual arrangement between you and IPM. |
| International Partnership for Microbicides, Inc. |
Silver Spring |
MD |
9/3/2010
|
| Contracts and Grants Coordinator |
| Candidates for this position should have the following education/experience and demonstrate mastery of the following knowledge, skills, and abilities:
Education/Experience
College degree or equivalent years of experience working with contracts or with related administrative experience.
Knowledge, Skills, and Abilities
â?¢ Proficient in Excel and other Microsoft applications.
â?¢ Experience working with finance or accounting tracking.
â?¢ Good organizational skills; proven ability to prioritize projects and initiate follow through with meticulous attention to detail and high-level accuracy.
â?¢ Ability to work effectively under pressure and handle multiple simultaneous tasks and demands.
â?¢ Good interpersonal skills; tact, patience, diplomacy, and appropriate assertiveness.
â?¢ Self-starter with ability to work independently and part of a team.
â?¢ Ability to interpret and explain complex issues and identify those with financial implications
â?¢ USAID experience preferred but not required
Position located at Headquarters in Silver Spring, MD. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
Silver Spring |
MD |
9/3/2010
|
| Controller |
| Education/Experience:
â?¢ Bachelorâ??s Degree in accounting/finance or business and a CPA, CFA or other professional designation preferred.
â?¢ A minimum of eight (8) years experience ideally gained through increasingly responsible position within Finance including accounting, auditing, and/or financial analysis. A minimum of two (2) years experience in accounting operations, which included a deadline-oriented closing process.
â?¢ Experience with not-for-profit accounting and small-company accounting environments.
â?¢ Experience in an international environment.
Knowledge, Skills, and Abilities:
â?¢ Working knowledge of financial reporting systems.
â?¢ High degree of proficiency with MS Office, particularly Excel.
â?¢ Knowledge of accounting procedures and internal control processes.
â?¢ Knowledge of OMB and FAR.
â?¢ Ability to understand, analyze, and explain financial information.
â?¢ Ability to research problems and present solutions and alternatives. Timely and effective problem solver.
â?¢ Good verbal and written communication skills. Ability to respond in clear and concise manner to requests and questions.
â?¢ Strong self-management skills. Ability to set well-defined and realistic goals; monitor progress and achieve results; manage own time and deal with stress effectively; manage multiple tasks and projects. Ability to plan work in accordance with general direction.
â?¢ Strong results orientation, i.e., the ability to work at a fast pace and meet critical deadline.
â?¢ Ability to manage multiple projects, goals and deadlines.
â?¢ Attentive to detail and accuracy. Thorough when performing work and conscientious about attending detail.
â?¢ Commitment to the delivery of excellent customer service â?? works and communicated with internal and external clients to satisfy their expectations. Committed to quality service.
â?¢ Ability to understand and control confidential information with absolute discretion.
â?¢ Team player, sense of humor, and excellent interpersonal communication skills.
â?¢ Tolerant of some ambiguity; work well under pressure; assertive; and well organized.
Position located at the Headquarters in Silver Spring, MD. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
Silver Spring |
MD |
9/3/2010
|
| Executive Assistant |
| Education and Experience
â?¢ Bachelorâ??s degree in business or related field highly desirable.
â?¢ Minimum seven years assisting senior level executives (preferable C-level) in positions that required maturity, poise, ability to handle highly confidential and sensitive information.
â?¢ Solid experience in communicating with high level stakeholders and constituents required.
â?¢ Experience in HR and/or legal environments helpful.
Knowledge, Skills and Abilities
â?¢ Outstanding time management and organization skills. Ability to multi-task, assess priorities and competently handle a variety of activities with a high-degree of accuracy.
â?¢ Advanced skills in Microsoft Office software applications (Outlook, Word, Excel and PowerPoint), web-based research and information collection, are essential.
â?¢ Excellent communication skills, both verbal and written, for internal and external communications.
â?¢ Ability to work and communicate with staff, consultants and other stakeholders through a variety of means to satisfy and address their expectations.
â?¢ Committed to quality service.
â?¢ Results oriented â?? able to work in a fast-paced environment and meet deadlines with competing priorities.
â?¢ Adept at archiving, organizing and retrieving material effectively.
â?¢ Strong ability to proofread and edit written material for sense, order and the correct use of grammar and punctuation.
â?¢ Superior attention to detail and conscientious about accuracy of work product.
â?¢ Highest level of confidentiality and professionalism required. Must be circumspect, tactful and diplomatic in all interactions.
â?¢ Tolerant of some ambiguity; work well under pressure; assertive, yet respectful.
Position is located in Silver Spring Maryland. IPM is an Equal Employment Opportunity employer. |
| GE Healthcare |
na |
MD |
9/3/2010
|
| Site Director -Scientific Asset Service Program |
|
* Bachelors degree in Electrical Engineering, Electronic Technology or related technical field; OR Associates Degree in Electronics and 3 years experience servicing electronic equipment in the field
* Previous management of direct reports, leadership, or supervisory experience
* Strong computer competency with solid understanding of Microsoft operating systems (Windows 2000, Windows XP) and Microsoft Office.
* Must be able to lift at least 40 pounds
This position is open to candidates within GE.
GE will only employ those who are legally authorized to work in the United States for this role.
Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Bachelor of Science Electrical Engineering Technology with college level courses in Biochemistry/Biology
* Ability to drive organizational change and process improvement
* At least 3 years experience with direct report or leadership responsibilities
* Familiarity with GLP/GMP requirements and/or IQ/OQ.
* Proven ability to develop and execute multiple priorities and approaches to meet objectives and experience in matrix organization
* Field service background and knowledge of Life Sciences market and instruments
* Working knowledge of asset management program
* Excellent communication skills, both written and verbal
* Ability to engage and motivate teams
* Strong verbal and written communication skills
|
| GE Healthcare |
na |
MD |
9/3/2010
|
| On-Site Engineer |
|
* Associates Degree with at least 2 years experience servicing electronic equipment, or equivalent military education or a High School Diploma/GED and 5+ years experience servicing electronic equipment.
* Must have experience servicing major OEM Life Science equipment.
* Willingness to take a drug test
* Must have a valid driver's license
The applicant must submit to GEHC's standard background check at the time of hire and must be legally authorized to work in the United States. This position may, in the future, support GEHC contracts with the U.S. government. In doing so, the successful candidate must submit to and clear a governmental background check.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Service experience with any of the following systems: HPLC, GC, LCMS, Mass Spectrometers, Liquid Handlers, PCRs, Plate Washers/Readers or Flow Cytometers
* Bachelor degree in electronics, computer science, or life sciences is desirable.
* Extensive computer and software knowledge.
* Proven successful customer service experience.
* Proven professionalism and leadership qualities.
* Strong written and verbal communication skills.
|
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Modality Leader - Research Sciences |
|
* BS Degree in a Life Science discipline such as Biology, Microbiology, Chemistry, Biochemistry, Genetics, Molecular Biology, Chemical Engineering
* A minimum of 7 years of life sciences sales management experience, key account management, sales management, marketing , scientific support and/or training
* Demonstrated basic computer skills in Microsoft Word, Excel, PowerPoint, Outlook or equivalent
Overnight travel is required
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* MBA
* Masters or PhD. in Scientific field
* Relevant sales management experience preferred (8+ years)
* Experience working in a laboratory setting
* Willingness and ability to take on additional responsibilities and undertake challenging tasks and/or global projects
* Proven ability to interact and influence cross functionally at all levels internally and externally
* This position requires a high degree of self-motivation.
* The candidate must possess a sense of what is most important and needs to be done next, while maintaining a ?customer first? attitude
* Ability to prioritize activities to ensure customer satisfaction and at the same time maximize profits is required
* Talent for getting along with and working productively with a variety of highly motivated sales personalities
* Experience and ability to develop and implement the global strategy and structure in line with business strategy
* Time management, organizational, and administrative skills
* Relevant experience in a life science marketing role
* Advanced degree in Life Science related curriculum and business administration.
* Ability to consolidate and communicate insights in an actionable way to facilitate growth; understand rationale of management requirements and translate into key takeaways
* Excellent communication skills and ability to interface with senior management.
* Proactive, self-starter that will both execute and identify opportunities to add value/insights to the leadership team and make process improvements to drive efficiencies.
* Ability to multi-task in a dynamic growth-oriented environment
|
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Key Accounts & Team Manager |
|
- BA/BS degree in Business or Technical Discipline.
- At least 5 years of leadership experience in corporate world or military
- At least 5 years experience in a Customer Service or Call Center Environment
- At least 2 years managing key or strategic accounts
- Direct customer relationship experience
- Demonstrated leadership experience through managing, supervising or training team members
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
- MBA
- Proven leadership and ability to orchestrate resources and motivate teams.
- Strong business acumen.
- Ability to develop and execute multiple priorities and approaches to meet objectives
- Exceptional interpersonal skills
- An inclusive leader that builds a connection to the workforce through personal involvement and trust
- Proven ability to influence and drive change through exceptional written and verbal communication skills
- Demonstrated tendency to challenge the status quo and drive constant improvement in process and ability to achieve organizational goals
- Understanding of customer/marketplace and drivers that influence customer behavior
- Previous direct report management/leadership experience
- Ability to resolve complex issues within functional area and/or area of expertise
- Ability to develop and execute multiple priorities and approaches to meet objectives
|
| GE Healthcare |
na |
CA |
9/3/2010
|
| Sales Representative 1-HC |
|
* Bachelor of Science Degree in a Life Science/Sciences
* 2 or more years sales experience within a Life Sciences or Medical Device industry
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Experience with distributor sales
* Experience working in and managing client in a laboratory environment
|
| GE Healthcare |
na |
CA |
9/3/2010
|
| Regional Sales Director - West Region |
|
* A minimum of 5 successful years selling ion the life sciences market
* Demonstrated success in sales strategy development and implementation
* A bachelors degree
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Excellent communication, presentation, and interpersonal relation skills
* Demonstrated negotiation skills
* Strong sales data analysis skills
* Proven ability to manage a budget
* Goal focused leader capable of building a strong teamwork environment
|
| GE Healthcare |
na |
NJ |
9/3/2010
|
| Account Manager , Research Sciences |
|
* BS degree in Biology, Chemistry, Biochemistry, or Chemical Engineering and/or BS/BA with relevant experience in Life Sciences.
* Minimum of 3 years successful commercial experience performance that exceeded plan: Including but not limited to sales, marketing, technical support, field applications support.
* Sales Training Experience: Commercial Selling Skills Training.
* Computer Literacy: Microsoft and Outlook
* Good interpersonal and communication skills, plus experience of using these skills to participate in cross-functional teams.
* Fluency and effective speaking skills in relevant local language.
* Self-Motivated, a team player and well organized.
* Overnight travel is required.
* This is a home office based sales position and as such the candidate must reside within 50 miles of the specified territory in order to support this role.
* To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must be willing to submit to a check of your driving records.
You must be willing to submit to a background investigation, including for example, verification of your past employment, criminal history and educational background.
* You must be willing to take a drug test.
* You must be willing to work out of a home office based in the specified territory.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* MBA
* Practical chromatography/imaging/filtration lab experience.
* Sales Experience with biotechnology/pharmaceutical industries in Life Sciences research.
* Strong presentation skills.
* Proven effective sales record in previous positions.
* Direct employment in biotech
|
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Americas EHS Leader (Life Sciences) |
|
* Bachelor of Science in Environmental, Civil, or Chemical Engineering, Hydrogeology or Geology or related technical discipline
* 5 years experience managing environmental site characterization investigations (Phase I, II, etc), remedial investigation, feasibility study, remedial design, risk assessment, remediation, demolition, decontamination, etc.
* Regulatory knowledge and experience working under U.S. federal and state and /or equivalents regulations covering contamination, site investigation and property transfer such as CERCLA, RCRA, OSHA, TSCA, ISRA, etc. and capable of learning requirements and applying this experience internationally
* Compliance experience with federal and state EHS regulations (CAA, CWA, OSHA, codes, etc)
* Proven project and program management skills
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Advanced degree (MS) and/or professional certifications (PG, PE, LSP, etc)
* Experience managing projects and/or EHS compliance in Europe or Asia and familiarity with European and Asian environmental laws
* Able to simultaneously manage multiple projects and other responsibilities, adjust to changing priorities and to make decisions with speed and accuracy based on available information
* Team player with strong interpersonal skills, capable of working within a globally diverse, cross-functional, internal and external team across different time zones
* Excellent oral and written communication, presentation, and negotiation skills
|
| GE Healthcare |
na |
WA |
9/3/2010
|
| Account Manager - Life Sciences Capital Equipment |
|
* You must be willing to work out of a home office and able to service the NW US territory. (Washington and Oregon)
* Bachelor?s degree in a scientific field.
* 3 or more years of experience in Life Sciences in the areas of Protein Detection and analysis with special focus on imaging and scanning.
* 3 or more years of commercial sales OR capitol equipment experience
* Computer Literacy: Microsoft and Outlook
* Overnight travel is required.
* To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must be willing to submit to a check of your driving records.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* BS degree in Biology, Chemistry, Biochemistry, or Chemical Engineering
* MBA
* Willing to work out of a home office in Seattle WA.
* 2 or more years laboratory experience or clinical experience.
* Sales Experience with biotechnology/pharmaceutical industries in Life Sciences research.
* Sales Training Experience: Commercial Selling Skills Training.
* Proven effective sales record in previous positions.
* Direct employment in biotech or pharmaceutical research, production or process development environment.
|
| GE Healthcare |
Northampton |
MA |
9/3/2010
|
| Quality Control Manager |
|
1. Bachelor?s degree (or high school diploma/GED plus 4 years of related work experience)
* At least 3 years of experience working in one of the following areas: regulated medical device, regulated pharmaceutical environment, quality control/assurance, or regulatory assurance
* At least 1 year of management experience to include direct reports
* Ability to effectively communicate using English (or local language)
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Demonstrated managerial experience
* Bachelors of Science in a related discipline (electronics, mechanics, thermodynamics, biochemistry)
* Leadership and motivational skills
* Organizational skills
* Fine attention to Detail
|
| GE Healthcare |
na |
MD |
9/3/2010
|
| Planner/Scheduler |
|
* At least two years of experience in an administrative support or coordinator role
* High School Diploma
* Demonstrated computer skills, including Microsoft Outlook, Word & Excel
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* MS Access or other database experience
* Understanding of the Life Sciences Industry and service delivery
* Experience negotiating with Original Equipment Manufacturers and Vendors
* Inventory management experience
* Effective written and verbal communication skills
* Ability to Work independently with minimum direction
* Must be willing to walk and climb stairs as necessary
* Must be willing to enter laboratory work environments as needed
* Ability to work in a matrix environment
* Strong Interpersonal Skills
* Knowledge of a parts ordering System
* Fluent in English Language
* Ability to identify problems and support action plans for problem resolution
|
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Scientist II-HC |
|
Bachelor?s degree in Biology, Chemistry, Engineering or related Life Science discipline
- 5+ years bioprocess experience in a (bio)chemical laboratory in an industrial setting
- Willingness to travel up to 25-50%
- Prior experience interacting with Customers
- Demonstrated ability to troubleshoot bioprocesses
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
- Master's degree in Biology, Chemistry, Engineering or related Life Science discipline
- Strong industrial experience in purification of biomolecules (upstream, downstream, technology transfer, validation, process development, biomanufacturing)
- Working experience in industrial biopharmaceutical purification
- Experience with chromatography techniques: IEX; HIC; AC; RPC; IMAC and SEC
- Experience with filtration methods- Experience in Disposable biomanufacturing
- Strong Background in the purification of biomolecules
- Experience in working in cGMP environment
- Working knowledge of FDA/EMEA regulations for biologics (Phase I-III manufacture)
- Proven skills working in a global team with global Customers
|
| GE Healthcare |
Westborough |
MA |
9/3/2010
|
| Project Leader, Black Belt |
|
Education/Knowledge:
* Degree in Mechanical engineering, plastics engineering, or a related field
* BS with a min of 10 years relevant industry experience or MS with a min. of 6 years of relevant industry experience
* Strong analytical and quantitative statistical skills; facility with Six Sigma concepts and tools
* Working understanding of regulatory issues related to Biopharmaceutical manufacturing and licensure related to medical devices
Skills:
* Negotiation, communication, presentation and listening skills
* Fluency in written and spoken English
Standard Microsoft Office packages and statistical software
Basic project management
Experience:
Work in a regulated environment (e.g., GMP or ISO quality system)
Other:
Authorization to work in the USA
Ability to travel domestically and internationally on an occasional basis
Ability to perform physical tasks that require mobility, manual dexterity, and visual acuity
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Change agent with strong credibility and influence in the organization
* Masters degree in business related field
* Demonstrated ability to motivate others and achieve results
* Demonstrated commitment for process improvement and product quality
* Customer-focused in defining quality and establishing priorities
Strong oral and written communication skills
Strong interpersonal and leadership skills
Executive level presentation skills
|
| GE Healthcare |
na |
CA |
9/3/2010
|
| Account Manager - Forensics & Human Identity |
|
* Bachelor of Science Degree in a Life Science/Sciences
* 2 or more years sales experience within a Life Sciences or Medical Device industry.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Demonstrated experience within the Forensic/Human Identity Market
* Experience working with DNA testing products
* Candidate must reside within specified territory (Western US)
|
| GE Healthcare |
Piscataway |
NJ |
9/3/2010
|
| Global Marketing Director - Cell Therapy Devices |
|
* MBA or Master?s degree in Marketing, Business Administration or comparable experience
* Undergraduate degree in a life sciences or medical field of study
* 8+ years experience in product marketing or product management of medical devices for regenerative medicine, or related field
* 3 or more years experience in a leadership role with direct reports and budget responsibility
* Must be able to work flexibly and travel up to 50% of time (25% overseas)
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Experience in regulatory affairs around and/or manufacturing of medical devices and/or cell therapy
* 5+ years Product development expertise, including: NPI process, product roadmap development, product life-cycle management
* Demonstrated project management skills
* Excellent oral and written communications skills
* Proven ability to network and influence to engage customers in an early dialogue
* Proven ability to grasp complex scientific and medical concepts
* Leadership skills to lead teams and shape/lead growth vision and marketing strategy
* Innovation ? develop new ideas through collaboration and execute on creative ideas
* Negotiation skills to work collaboratively with existing customers and engage in discussions with new external parties
* Experience working within a global matrix environment
* Documented analytical skills to clearly develop, evaluate, and present options and business cases
|
| GE Healthcare |
na |
MD |
9/3/2010
|
| Field Service Engineer |
|
* Bachelor?s degree, Electrical Engineering, Electrical Engineering Technology, equivalent military education or Associates Degree with 2 years experience servicing electronic equipment, or a High School Diploma/GED and 12 or more years experience servicing electronic equipment.
* Experience interfacing with both internal team members and external customers as part of a solution based service process.
* Experience diagnosing and repairing mechanical, electromechanical, and/or electronic equipment.
* Experience troubleshooting and responding to customer concerns.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
Excellent analytical and communication skills with the ability to communicate complex technical issues in an easy to understand manner
* Six Sigma trained/certified
* Change agent and process oriented.
|
| GE Healthcare |
na |
CA |
9/3/2010
|
| Product Specialist ? Filtration and Single-Use |
|
* This is a home office based sales position and as such the candidate must reside within their territory in order to support this role.
* Bachelor?s degree in chemical engineering or mechanical engineering.
* 3+ years of hands-on experience with BioProcess filtration and/or fluid-handling technologies
* Excellent oral presentation and technical writing skills.
* Overnight travel, up to 50%, is required.
To the extent that you are applying for a position that requires you to operate a GE owned/leased, privately owned/leased or rental vehicle for company business, you must have a valid drivers license and be willing to submit to a check of your driving records.
GE will only employ those who are legally authorized to work. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics
* Working knowledge of UNICORN
* Hands-on experience in process development for sizing and optimizing filtration processes
* Strong background in the use of single-use products for normal-flow filtration, cross-flow filtration and fluid handling.
* Technical sales or sales support experience or direct employment in a biotech or pharmaceutical production or process development environment.
* This position requires a high degree of self-motivation and prioritization skills. The candidate must also have a talent for getting along with and working productively with a variety of highly motivated sales personalities.
|
| AstraZeneca Pharmaceuticals |
Houston |
TX |
9/4/2010
|
| Regional Sales Director - CV - Cleveland OH |
| Qualifications:
*Bachelor's degree.
*Minimum of 10 years experience in pharmaceutical sales or healthcare, must have management experience in field sales.
*Ability to identify strategies with greatest business impact, formulate an appropriate business plan and enroll their teams to execute the plan.
*Demonstrated leadership and communication competencies, and experience in managing budgets are required.
*Thorough understanding of customer segments and regional market dynamics within all therapeutic areas.
*Ability to lead and manage district sales leaders and to develop staff through coaching and mentoring.
*Exhibited ability to manage multiple, concurrent work-streams in diverse functional/therapeutic areas.
*Previous successful work experience in team selling environments, inclusive of successful management of teams.
*Demonstrated presentation and negotiation skills.
*MBA and/or prior experience in multiple commercial functions (e.g. Marketing, Managed Markets). |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Director Clinical Research-Alzheimer's Disease |
| Requirements --Education and Experience
o Medical doctor with specialty training and board certification in adult neurology with significant experience in Alzheimer's drug development (PhD candidates with extensive clinical experience may also be considered).
o Experience in clinical and preclinical science in Alzheimers disease.
o Greater than 5 years of drug development /commercialization experience (the majority of which should be in industry) with clear evidence of delivery
o Ability to balance business and clinical research objectives is critical
o Thorough understanding of pharmaceutical safety reporting and surveillance processes
o Experience working with regulatory agencies and preparing regulatory documents
Skills and Capabilities
o Strong team-working skills and an ability to work in a global pharmaceutical environment
o Strategic thinking
o Strategic influencing
Organizational Behaviors
o Foster behaviours that reinforce AZ as a global organization
o Ensure respect for different practices and expertise in different environments
Leadership Capabilities
o Passion for Customers
o Thinks Strategically
o Acts Decisively
o Drives Performance
o Works Collaboratively
o Develops People and Organization |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sourcing Manager - Learning |
| * Bachelors Degree
* 5 years' work experience
* Minimum of two to three-years procurement experience, strategic sourcing experience is preferred
* Ability to effectively and clearly present information and respond to questions from a wide variety of audiences including groups of senior executives, middle managers and hourly personnel within the company or at supplier/customer engagements.
* Project (sourcing) background in most, if not all, key categories of commercial spend, such as Agency, Media, Market Research, Medical Education, Conferences, Print, Premiums and Direct Marketing is necessary
* Experience with e-procurement is preferred
* Understanding of contract development and business law is required.
* Minimum of two years experience negotiating contracts.
* Proved ability to manage multiple projects/tasks effectively
* Strong written and verbal communication skills
* Proficiency in Microsoft Word, Power Point and Excel
* Demonstrated success working in a team environment
* Strong analytical and organizational skills
* Proficiency in Procurement and other business related systems, e.g. ERP, Ariba
* Financial Analysis, e.g.
- Dun & Bradstreet reports
- Credit Scoring |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Audit Consultant |
| Minimum Requirements --Education and Experience
The position requires an understanding of the business and of internal audit practice.
The minimum requirements for the role holder are as follows:
o Relevant business experience through job placements -- able to demonstrate own experience (successes and failures) of governance, compliance, risk management and control
o Able to demonstrate examples of cross-functional working
o Must have demonstrable capability of understanding of financial and internal controls and systems, risk management, governance and compliance with laws, regulations and policies
o Experience of (or able quickly to learn) key internal control frameworks, audit methodologies and practices
o Educated to bachelors degree level and possibly studying for a post-graduate qualification e.g. MBA or professional accountancy/auditing qualification
o Fluent English (written and verbal)
Business Communication and Relationship Management: Able to build and maintain effective working relationships with key business managers to effect business change under challenging circumstances. Is able to communicate messages and proposals clearly obtaining buy-in for change.
Governance and Compliance: Adheres to and complies with AZ policies and procedures and has appropriate knowledge of such appropriate policies and procedures in order to advise and influence management on its application and improvement.
Risk Management and Assurance: Supports and challenges the business to understand and quantify the impact of strategic, operational, financial and compliance risks.
Specialist Knowledge and Skills: Increased level of knowledge of function areas (beyond normal business mastery expected of all staff) in order to provide Subject Matter Expertise to audits. Analytical ability to identify facts and issues and make decisions based on this and the wider business context.
Assignment Management: Deliver audit assignments to desired objective obtaining business change and influence. Audit peer review and application of business context and knowledge to ensure focus on important issues. Continually develop GIA department.
Managing and Developing the Audit Plan: Develops and delivers audit plan to provide assurance to audit committee on strategic, operational, financial and compliance risk areas, using range of techniques, business knowledge and monitoring tools.
Other Role Specific Skills:
o Demonstrate high levels of personal integrity, independence and tenacity
o A creative and independent thinker
o Ability to understand business areas and the political environment in which they operate
o Demonstrate the ability to learn quickly across SET areas when placed in new situations/functional environments
o Ability to contribute personal judgement in relation to business and audit issues
o Excellent communication skills to enable risks, issues and actions to be conveyed in a compelling and understandable way
There will be an expectation of reasonable levels of travel to fulfil this role. |
| AstraZeneca Pharmaceuticals |
Westborough |
MA |
9/4/2010
|
| Sr. Financial Analyst |
| Minimum Requirements:
* Bachelor's Degree in Accounting or Finance
* Minimum 8 years of accounting/finance experience of which 5 years are in a manufacturing environment
* Advanced understanding of accounting principles required
* Strong analytical skills with the ability to analyze complex issues and develop recommendations
* Strong Business Partnering skills
* Strong communication, presentation & organizational planning skills required
* Proficiency in PC spreadsheets and database applications
* Previous experience with SAP general ledger and project accounting preferred
* Ability to lead and influence cross functionally
* Demonstrated ability to work in a dynamic work environment
* Strong drive for results
Preferred Background:
* MBA and/or CPA preferred
* Manufacturing experience preferred |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Medical Information Manager |
| Qualifications:
* Advanced degree in Pharmacy (PharmD preferred), Pharmacology, Science or equivalent clinical experience
* Pharmacy Licensure preferred
* 2+ years experience in pharmaceutical industry based Drug Information Delivery or equivalent industry experience
* Demonstrated expertise in drug information communication and management
* Excellent oral and written communication skills and interpersonal skills
* Knowledge of FDA requirements
* Ability to apply Regulatory and Compliance guidelines to Drug Information delivery
* Understanding of the information needs for various customer segments
* Project Management leadership experience
* Strong leadership ability
Preferred Background
* Clinical Pharmacy experience with patient care exposure
* Drug Information Residency or equivalent experience
Skills and Competencies
* Expert Scientific Knowledge
* Leadership Skills
* Drug Information Management Expertise
* Regulatory and Compliance Expertise
* Organization Savvy
* Communication Skills
* Presentation, Facilitation and Instructional Skills |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sourcing Manager |
|
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Associate Director Quality Assurance Pharmaceutical Development |
| Minimum Requirements -- Education and Experience
Functional & Business knowledge
Experience, Functional Knowledge, Business Knowledge, Education, Specialist Skills
* A BS degree with extensive experience (5-10 years) of working within a pharmaceutical GMP
environment, preferably within a pharmaceutical development organisation
* A minimum of 3 years of managing teams of people, preferred
* Experience from Quality Assurance Management is essential; a broad and comprehensive understanding
of Quality Systems and GMP
* A comprehensive understanding of the pharmaceutical/drug development process
* Good knowledge and reputation in the QA arena and specifically in GMP matters
Skills and Capabilities
* Excellent team working and networking skills and encourages team effectiveness
* Excellent at building and sustaining effective external relationships
* Demonstrates independent judgement and uses risk management in complex situations frequently
* Capable of making effective decisions, and communicating with conviction and inspiration
* Manages delivery effectively by setting well communicated goals and targets
* Demonstrates a good understanding of change management and effective application
* An good communicator with experience of interacting effectively across interfaces
* Able to demonstrate the drive and energy to establish the role and make a difference.
* Demonstrates a high degree of personal credibility
Leadership Capabilities
Passion for Customers: Manages multiple customer needs in a global and cross
functional environment, focused on ensuring proactive regulatory compliance
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action.
Uses deep insight to develop solutions that impact beyond the role/function.
Acts Decisively: Creates clarity for others to make decisions within clear boundaries by clarifying roles
and responsibilities
Drives Performance: Anticipates and/or removes obstacles for others; retains vision of
regulatory compliance and Quality System requirements. Removes obstacles so teams/workgroups
can deliver and succeed
Works Collaboratively: Creates shared purpose with suppliers and contractors across internal
boundaries by identifying and establishing common purpose and goals. Engage with key crossfunctional
stakeholders to deliver value to the business
Develops People and Organisation: Demonstrates a genuine commitment to the time and effort
needed to develop oneself and others for the long term.
For this role, the target level for all leadership capabilities is 3
Internal and External Contacts/Customers
* Advises Pharmaceutical Development Managers (leaders) on Quality Assurance matters
* Networks with other Quality Assurance leaders, across Operations Sites, GES, IS Integrated Assurance etc
* Has or develops contacts with local Regulatory Authorities
* Has or develops a network with counterparts in other companies
* Works in close collaboration with QA Development and QA Capability peers
Reporting Relationship
* Direct Reports: manages 3-4 QA staff
Budget responsibility
* Direct responsibility and control: $1.0 million
* Indirect influence and contribution: up to $ 30 million
Posting will close on Friday, 17 September |
| AstraZeneca Pharmaceuticals |
Philadelphia S |
PA |
9/4/2010
|
| Pharmceutical Sales Specialist - CNS SC2 - Philadelphia, PA |
| * Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
*Knowledge of medical equipment, territory management direct and in-direct sales processes
*Possess excellent written and verbal communications skills, and presentation skills
*Problem solving skills
*Business administration skills
*Laptop computer skills
*Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
*Proven ability to understand, internalize, and routinely present challenging scientific information
*Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world |
| AstraZeneca Pharmaceuticals |
Collegeville |
PA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Collegeville, PA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sales Trainer |
| - Bachelor's degree
- Minimum of 3 years experience in pharmaceutical sales or healthcare
- Experience in training, curriculum design, and delivery
- Thorough knowledge across therapeutic areas
- Demonstrated leadership, communication and organizational skills
- Thorough understanding of market dynamics within the therapeutic areas
- Demonstrated consistent success as a Pharmaceutical Sales Specialist
- Hospital or CVAS experience preferred |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| eArchivist |
| Qualifications:
* Bachelor's Degree (or equivalent) in Business Administration, Information Science, Archival Science or related discipline
* 4 years experience in a records or archives management role or an equivalent professional role within service related industry.
* Proven record of success in process and/or project management such as Green Belt certification.
* Proficient knowledge and experience of core archiving records management processes and information technologies.
* Business process analysis and improvement, lean (six sigma) thinking; preferably on global scale.
* Development of standard operating procedures, guidelines, best practices and systems documentation.
* Proficient knowledge and experience with Regulated or legal environment and clear understanding of regulatory requirements (e.g., GxP) and a demonstrated understanding of the drug development process.
* Development of training programs and materials, including computer based training preferred.
Skills:
* Demonstrated leadership capabilities at appropriate target level.
* Demonstrated project leadership, change management, presentation and organizational skills.
* Proven change management, interpersonal, communications, assertiveness and negotiation skills.
* Influencing and relationship skills to enable effective management of internal stakeholders and partners.
* Leading global or cross-functional projects. Ability to work in a diverse, global team.
* Good ability to express oneself in English, both verbally and in writing.
* Core archiving and records management processes and information technologies.
* Archiving and records management practices in the pharmaceutical industry (proficient).
* Product/service business case process includes developing, presenting, and defending the business case.
* Ability to provide accurate and concise data in a timely manner.
* Enthusiastic and self-motivated.
* Willingness to learn and try new ideas. |
| AstraZeneca Pharmaceuticals |
Houston |
TX |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - League City, TX |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
McAllen |
TX |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - McAllen, TX |
| EDUCATION:
* Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
*Knowledge of medical equipment, territory management direct and in-direct sales processes
*Possess excellent written and verbal communications skills, and presentation skills
*Problem solving skills
*Business administration skills
*Laptop computer skills
*Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
*Proven ability to understand, internalize, and routinely present challenging scientific information
*Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world. |
| AstraZeneca Pharmaceuticals |
Houston C |
TX |
9/4/2010
|
| Pharmaceutical Sales Specialist - Hospital - H1 H1A - Houston C, TX |
| EDUCATION:
Bachelor's degree
EXPERIENCE:
At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
Experience selling and knowledge of CNS products or diseases preferred
Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
History of building and influencing customer relationships, and goal achievement
Demonstrated clinical selling skills
Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
Knowledge of medical office equipment, territory management direct and in-direct sales processes
Possess excellent written and verbal communications skills, and presentation skills
Problem solving skills
Business administration skills
Laptop computer skills
Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
Proven ability to understand, internalize, and routinely present challenging scientific information
Ability to freely accept, implement, and exchange best practices. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Intern - Facilities Management Site Services |
| Minimum Requirements:
*Currently pursuing a four-year Bachelor degree in Architectural Engineering, Interior Design or Facilities Planning and Management. Would also consider Architecture, Construction Management, or other Engineering majors.
*PC proficiency: AutoCAD, MS Office, MS Outlook
This internship position is located at the AZ Waltham Facility in Boston, MA. |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Post Doc Intern - Cancer Chemistry |
| Requirements
*A PhD in Chemistry, Biophysics, or a related field.
*Expertise in continuum electrostatics, molecular dynamics simulations of proteins, or QM/MM calculations for biological systems
*Experience in structure-based drug design (e.g., docking and scoring, library design, homology modeling) a plus
*Strong programming/scripting capabilities (e.g., python, perl, OEChem toolkit) desirable
*Strong written and oral communication skills
*Ability to work well in multi-disciplinary teams
This position will be placed at AstraZeneca R&D Boston, USA |
| AstraZeneca Pharmaceuticals |
Waltham |
MA |
9/4/2010
|
| Post Doc Intern - Infection Chemistry |
| Requirements
*A PhD in Chemistry, Biophysics, or a related field.
*Expertise in continuum electrostatics, molecular dynamics simulations of proteins, or QM/MM calculations for biological systems
*Experience in structure-based drug design (e.g., docking and scoring, library design, homology modeling) a plus
*Strong programming/scripting capabilities (e.g., python, perl, OEChem toolkit) desirable
*Strong written and oral communication skills
*Ability to work well in multi-disciplinary teams
This position will be placed at AstraZeneca R&D Boston, USA |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Drexel Co-Op - Maintenance Engineering |
| Minimum Requirements · Engineering major. (Mechanical, Architectural or Electrical) · Completion of the first year of study is required. · Proficiency with Microsoft Windows Word, Excel and familiarity with Project. Skills and Competencies · The intern must have good interpersonal skills to work with design, construction, operational and maintenance personnel. The intern will also be required to interact with tenants. · An understanding of basic engineering concepts. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Intern - Corporate Communications |
| Minimum Requirements
-Second or third-year BA or BS candidate with communications, marketing or related field preferred
-Coursework completed includes communications, public relations, marketing and/or journalism
-Previous work or internship experience in a similar field preferred
-PC skills required, including proficiency in MS Word and MS PowerPoint; Willingness to learn and utilize new software programs and processes
-Ability to navigate digital media channels (Facebook, Twitter, etc.)
-Must be able to meet deadlines/balance multiple tasks at one time
-Presentation skills/professionalism |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Associate Research Scientist Epidemiology |
| Minimum Requirements --Education and Experience
(These may vary with specific prior experience, but will generally be as follows.)
* MSc or MPH in epidemiology, or a closely related public health field
* 3 years experience as an epidemiologist in the health care environment
* Good knowledge in epidemiological methodology and its applications in the health care environment
Skills and Capabilities
* Good knowledge of epidemiology study design and ability to critically appraise and synthesize epidemiological literature
* Ability to apply epidemiological techniques in the analysis of data
* Basic therapy area knowledge
* Thorough grounding in quantitative research methods
* Solid understanding of the epidemiology skills group and how it contributes to achieving the objectives of the business, plus a general understanding of other functions
* Ability to manage epidemiology projects, including change in project requirements and need to accommodate uncertainty
* Good analytical skills and judgment within industry and Company operating guidelines
* Ability to liaise with and influence others through solid communication skills, including those in other areas or departments
* Ability to present information for discussion at higher levels within the business
Internal and External Contacts/Customers
Examples include:
* Emerging Product Teams
* Global Product Teams
* Safety Management Teams
* Clinical Project Teams
* Preclinical Disease Area Teams or equivalent
Reporting Relationship
* Direct Reports - none
* Indirect Reports - none |
| AstraZeneca Pharmaceuticals |
Los Angeles N |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC2 - Woodland Hills, CA |
| * Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
*Knowledge of medical equipment, territory management direct and in-direct sales processes
*Possess excellent written and verbal communications skills, and presentation skills
*Problem solving skills
*Business administration skills
*Laptop computer skills
*Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
*Proven ability to understand, internalize, and routinely present challenging scientific information
*Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sr. Cost Analyst |
| Minimum Requirements/Preferred Background
* Good working knowledge and understanding of company policies and procedures.
* Demonstrated skills and ability in PC applications (advanced Excel knowledge) and in-depth knowledge of mySAP financial modules and applications.
* Bachelors degree in an accounting or business discipline with a MBA', CPA or CMA preferred. A minimum of 5 years related experience is desired
* Knowledgeable in cost management, strong analytical skills and strong systems' technical skills in order to effectively use PC spreadsheets and data base applications such as Hyperion and mySAP R3 applications.
* Excellent oral and written communications skills required to interact with various areas and management levels, both within and outside of AstraZeneca.
* Excellent interpersonal, organizational and time management skills. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Intern - Corporate Communications |
| Minimum Requirements
-Second or third-year BA or BS candidate with communications, marketing or related field preferred
-Coursework completed includes communications, public relations, marketing and/or journalism
-Previous work or internship experience in a similar field preferred
-PC skills required, including proficiency in MS Word and MS PowerPoint; Willingness to learn and utilize new software programs and processes
-Ability to navigate digital media channels (Facebook, Twitter, etc.)
-Must be able to meet deadlines/balance multiple tasks at one time
-Presentation skills/professionalism |
| AstraZeneca Pharmaceuticals |
Wausau |
WI |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Wausau, WI |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Sr. Contract Specialist |
| Minimum Requirements
* Bachelor's Degree and 4 years of relevant business experience.
* Excellent attention to detail to ensure successful contract execution that represent a portion of over $6 billion in annual customer discounts.
* Excellent organizational and time management skills with the ability to multitask in order to meet deadlines and provide exceptional internal and external customer support.
* Excellent oral and written communication skills.
* Proficient in Microsoft office applications, specifically Word and Excel, with the ability to adapt and learn query tools and new computer applications.
* Ability to manage daily workload as well as special assignments and projects and deadlines, and serve as a mentor to those at the Contract Specialist level, helping them to prioritize workload and understand individual customer needs and expectations.
* Demonstrated high level of professionalism with the ability to interface with all levels and departments of the organization
Key Leadership Capabilities
* Engages with internal and external customers through communication vehicles to better understand underlying issues/needs and proactively/consistently develops solutions, products or services.
* Ability to think strategically and think broadly, but also identifies opportunities and develops solutions.
* Works collaboratively by respecting and integrating diverse views into decisions/proposals. Works as an individual contributor to accomplish team goals and to support goals of others.
* Drives performance by anticipating and/or removing obstacles for others in order to deliver results and succeed.
* Acts decisively, making effective decisions under pressure and can do so in the absence of complete information.
Preferred Background
* Paralegal Certification from an ABA accredited institution and/or a Bachelor's Degree in a business related field (Finance, Law, Marketing, and/or Health Care).
* 2-3 years previous experience working in Managed Markets or the healthcare industry.
* In-depth knowledge of Pharmaceutical contracting processes
* Proven ability to build/maintain credible and strong relationships with internal/external customers and peers.
* Incumbent should possess a strong understanding of AstraZeneca's product line and competitors, and the various contracting strategies deployed across assigned markets. |
| AstraZeneca Pharmaceuticals |
San Diego |
CA |
9/4/2010
|
| District Sales Manager - CNS SC1 - San Diego, CA |
| Minimum Requirements
*Bachelor's degree.
*Minimum of 3+ years experience with consistent success in pharmaceutical sales or healthcare sales.
*Demonstrated leadership capabilities, financial management and written & oral communications skills.
Preferred Background
*Previous management experience.
*Previous exposure and/or experience in other functional areas of the business, i.e., Sales Training, Customer Solutions, Sales Operations, Managed Care and Marketing. |
| AstraZeneca Pharmaceuticals |
Santa Rosa |
CA |
9/4/2010
|
| Pharmaceutical Sales Specialist - MCL - Santa Rosa, CA |
| Education:
-Bachelors degree (any major) from an accredited college or university is required.
Experience:
- Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
- Demonstrated effective organizational and communication skills
- Leadership, self--motivation and initiative
- Demonstrated judgment and decision-making capability
- Be results oriented with demonstrated time management skills
- Ability to learn, analyze, understand and convey complex information
- Demonstrated technical aptitude and computer skills are essential
- A valid driver's license and safe driving record |
| AstraZeneca Pharmaceuticals |
Fort Collins |
CO |
9/4/2010
|
| Pharmaceutical Sales Specialist - CNS SC1 - Fort Collins, CO |
| EDUCATION:
* Bachelors degree
EDUCATION:
* Bachelors degree
EXPERIENCE:
*At least two years of documented, full-time, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment; or five years of experience in treating patients with CNS disorders, or in another CNS related business discipline.
*Experience and knowledge of CNS products and disorders, especially those associated in treating the chronic mentally ill.
*Experience selling and knowledge of CNS products or diseases preferred
*Experience selling in retail and non-retail settings including mental health clinics, hospitals, and office-based private practices.
*History of building and influencing customer relationships, and goal achievement
*Demonstrated clinical selling skills
*Demonstrated ability to manage PREP budget and to work through the PRA process
ADDITIONAL SKILLS:
*Knowledge of medical equipment, territory management direct and in-direct sales processes
*Possess excellent written and verbal communications skills, and presentation skills
*Problem solving skills
*Business administration skills
*Laptop computer skills
*Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
*Proven ability to understand, internalize, and routinely present challenging scientific information
*Ability to freely accept, implement, and exchange best practices
COMPANY:
AstraZeneca is a global leader in the research, development and marketing of gastrointestinal (GI), oncology (ONC), anesthesia/pain management (PAIN), cardiovascular (CV), central nervous system (CNS) and respiratory (RESP) products. Leveraging our powerful science-based culture, strengthened R&D platforms, and enhanced worldwide marketing/sales assets; AstraZeneca has emerged as one of the leading pharmaceutical companies in the world. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| IS Business Analyst - Sr. Manager |
| Skills and Capabilities (Minimum Requirements)
* BS degree Business Administration or Information Science
* Minimum 5 or more years in technology or process consulting.
* Knowledge of external technology trends and / or business functions, business data and current applications and systems.
Preferred Background
* 8 + years IS management in project management and customer relationship management
* Knowledge of the pharmaceutical / healthcare industry
* Experienced in process modeling or technology consulting
* User Experience expertise
* Pharmaceutical Marketing experience
* Siebel CRM experience
* Data warehousing experience
Leadership Capabilities
* Passion for Customers. Level 2 -- Engages Customer in Development of Solutions: individual seeks to understand underlying issues/needs and proactively engages the customer in development or identification of solutions, products or services.
* Thinks Strategically. Level 2 -- Applies a Broad Perspective: individual thinks more broadly than their role (e.g. externally) and uses this insight to challenge and adapt current approaches/ ways of doing things.
* Acts Decisively. Level 2 -- Makes Effective Decisions Under Pressure: individual still makes effective decisions and can do so in the absence of complete information and when under pressure.
* Drives Performance. Level 2 -- Holds Other Accountable: individual holds others accountable for high standards and clarifies what needs to be accomplished, why, and the consequences for the individual and/or the organization.
* Works Collaboratively. Level 2 -- Respects and Integrates Diverse Views: individual seeks input and demonstrates an appreciation for diverse views by incorporating them into decisions/ proposals.
* Develops People and Organisation. Level 2 -- Provides Behavioral Feedback: individual has an objective view of others' capability and provides coaching and feedback in the moment, while continuing to develop him/herself.
Core Capabilities
* Business Awareness/Acumen. Level 3 -- Demonstrates a full awareness and understanding of the challenges and opportunities facing own, AstraZeneca and customers businesses.
* Change Management. Level 3 -- Demonstrates a working knowledge of change management that recognizes and addresses different areas of change (e.g. people, process and technology).
* Challenge and Influence. Level 3 -- Encourages others to remain flexible and demonstrate own flexibility when considering options and the impacts.
* Communication and Facilitation. Level 3 -- Anticipates reactions to messages and adapts communications accordingly and deals positively with others' resistance.
* Innovation. Level 3 -- Stays current on emerging trends and new practices, and applies knowledge where applicable.
Professional Capabilities
* Business Information Management. Level 3 -- Utilizes business acumen in working with business leaders to design improved services, processes and assets for effective knowledge and information dissemination.
* Internal Consultancy. Level 3 -- Develops a collaborative relationship with internal clients and works with them to achieve joint objectives and targets.
* Portfolio Management. Level 2 -- Demonstrates a working knowledge of the services and project prioritization process within IS.
* Requirements Management. Level 3 -- Effectively uses requirement gathering tools, methods, processes and techniques that assist the business user to better visualize what is required (e.g. through scenario analysis, prototyping, etc.)
* Solution Design (Functional). Level 3 -- Demonstrates a sound working knowledge of the business functional area of responsibility (e.g. how people work and the business currently operates) to identify and recommend appropriate solutions.
* Solution Testing. Level 3 -- Demonstrates firm knowledge of AstraZeneca testing standards to design test documentation (test scripts, test conditions, and expected results for test plans) that enable accurate testing of AstraZeneca application requirements and minimize test-cycle time. |
| AstraZeneca Pharmaceuticals |
Wilmington |
DE |
9/4/2010
|
| Senior Manager, Government Pricing & Analytics |
| Minimum Requirements
*Bachelor's Degree
*Minimum of 7 years experience in pharmaceutical or healthcare industry, public or private contracting, or consulting; 2 years direct people management experience.
*Strong knowledge of pharmaceutical contracting, pricing, marketing/sales, or finance.
*Demonstrated abilities to influence without authority, lead teams and develop/foster relationships with senior leadership.
*Strong communication (oral & written) and analytical skills with excellent attention to detail.
*Ability to manage multiple priorities and strong organization skills.
Skills and Competencies
*Knowledge of Government and Medicaid contracting and claims/discount processes.
*Ability to think strategically and broadly, using this insight to challenge and adapt current approaches / ways of doing things.
*Works collaboratively by respecting and integrating diverse views.
*Drives performance by anticipating and/or removing obstacles for others in order to deliver results and succeed.
*Acts decisively and makes effective decisions and can do so in the absence of complete information and when under pressure.
*Thorough understanding of the AstraZeneca product line, key government reporting requirements and the various contracting strategies deployed across markets.
*Skilled in utilizing information technology and systems, working with spreadsheets, databases, and decision support and query tools, specifically Excel and MS Word
Preferred Background
*MBA
*An educational or professional background in Government and/or Medicaid systems or finance.
Internal and External Contacts/Customers
*Account Directors
*Contracting Directors
*Strategy Managers
*Legal
*Finance
*Information Systems
*State & Government Affairs
*Brand Teams
*AstraZeneca contracted customers, specifically Federal and State Government Agencies
*Outside legal counsel
*Outside industry experts
Reporting Relationship
*Direct Reports -- 1 Govt Pricing Manager and 3 Govt Pricing Analysts
*Indirect Reports - N/A |
| AstraZeneca Pharmaceuticals |
Woodbridge |
VA |
9/4/2010
|
| Pharmaceutical Sales Specialist - Hospital H1_H1A - Woodbridge, VA |
| Qualifications: EDUCATION: Bachelor's degree EXPERIENCE: At least tw |
