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Search Jobs by Category
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director**- Clinical Research- Brilinta Brand Team |
Requirements ? Education and Experience**
· Graduate of a recognized school of medicine with an M.D. degree or equivalent.
· Specialty training and board certification in Internal Medicine; Specialty Certificationin Cardiovascular Medicine highly desireable.
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in cardiovascular disease especially in the area of thrombosis. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
· An understanding of the interplay between clinical development and commercial objectives.
· Excellent presentation skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
 |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director** Clinical Research- Crestor/Certriad Brand Team |
| · Graduate of a recognized school of medicine with an M.D. degree or equivalent.
· · Specialty training and board certification in Internal Medicine; Pediatrics (with appropriate subspecialty); Endocrinology; Diabetes and Metabolism; or Cardiovascular Medicine .
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry for Director level position. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
· An understanding of the interplay between clinical development and commercial objectives.
· Excellent presentation and interpersonal skills skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Mechanic II |
| ? High school diploma
? 3 years of active, hands-on experience in the installation, maintenance, repair and troubleshooting of refrigeration and HVAC/R equipment in commercial, industrial, manufacturing or research facilities.
? Completion of two or more years of a state accredited Journeyman program in HVAC/Refrigeration or equivalent technical program.
? Demonstrated ability with analytical/troubleshooting skills in HVAC controls (DDC and pneumatic) and refrigeration equipment
? Possess a valid EPA 608 Universal Certificate
? Demonstrated ability to make sound decisions and deal effectively with internal customers independently.
? Demonstrated ability to successfully complete complex assignments from start to finish
? Demonstrated ability to work independently and using safe work practices.
? Strong teamwork, interpersonal, communication, and writing skills
? Basic computer skills.
Preferred Background
? Completion of a state accredited Journeyman program or equivalent Associates degree in an HVAC engineering technology program
? 5+ years of active, hands-on experience in the HVAC/Refrigeration trade
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Financial Planning & Reporting Manager (Multiple Vacancies) |
| ? B.S. Degree in Finance or Accounting
? 7+ years financial experience, pharmaceutical industry experience preferred
? Knowledge of US operating model
? Excellent PC skills and experience including SAP, BW, Excel and Powerpoint
? Strong analytical ability
? Exceptional communication and interpersonal skills, including oral and written
? Demonstrated ability to perform in an environment that emphasizes teamwork
? Demonstrated ability to lead a process with minimal or no supervision
? Ability to influence others without authority
? Demonstrated capacity to effectively manage multiple and frequently changing priorities
? High degree of accuracy with attention to detail
? Demonstrated ability to meet strict deadlines
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Learning Specialist |
| ? Bachelor?s degree, preferably in a learning and development or related field (e.g., education, instructional design, instructional technology, human performance improvement (HPI), organization design) with 5 or more years experience in a pharmaceutical or related field in some aspect of strategic learning management
? Effective communication, presentation, organizational & interpersonal skills.
? Strong understanding of adult learning theory, instructional design and a variety of learning methodologies.
? Demonstrated internal consulting skills and ability to facilitate and provide feedback with employees and leaders at all levels.
? Good project management, problem-solving and decision-making skills.
? Ability to perform well in a team-based environment.
? Ability to align learning initiatives with strategic objectives
Preferred Background
? Bachelor?s degree in a development/training/learning discipline with 5 or more years of management/supervisory experience.
? Involvement in industry groups with specializations in effective learning management and training.
? Working knowledge of cGMP?s and Safety, Health and Environmental regulations or experience working in a regulated environment
? Working knowledge of Lean and 6 sigma
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Patient Safety Principal Scientist Compliance and Support |
| Minimum Requirements ?Education and Experience:
?Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background with proven competence in Patient Safety/Clinical Development
?At least 5 years Patient Safety and/or Clinical Development experience
?High level of technical competence, with an ability to balance this with industry standards to achieve business goals
?Proven leadership skills, able to resolve conflict
?Able to work with a high degree of autonomy
?Able to work effectively as a member of a cross-functional or global team
?Comprehensive understanding of Patient Safety regulatory obligations
?Able to represent AstraZeneca externally where required
?Able to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
?Demonstrable professional excellence ? adds value by applying expertise proactively
?Proven good communication skills with ability to work across cultures
?Able to influence whilst maintaining independent and objective views
?Maintains high ethical standards, including a commitment to AstraZeneca values and behaviors
?Good attention to detail
?Good time management
?Fluent in English
?Computer literate
Organizational Behaviors:
?Passion for Customers
?Drives Performance
?Works Collaboratively
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Medical Director- Patient Safety- Respiratory and Infection/GI Therapy Area |
| Requirements ? Education and Experience
? Medical degree
? At least 2 years of clinical experience post-registration/certification
? High level of medical competence, with an ability to balance this with industry standards to achieve business goals
? Two or more years of Drug Development/Pharmacovigilance experience obtained while working in industry and/or academia
? A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities is preferred
Skills and Capabilities
? General medical/therapeutic area knowledge
? Ability to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
? Ability to influence whilst maintaining independent and objective views
? Excellent communication, interpersonal and organizational skills
? Attention to detail
? Delivery focus
Organizational Behaviors
? Integrity and high ethical standards
? Excellent team-working skills
? Ability to appreciate diversity and work as equals with global and cross-functional teams
? Customer-focused
? Demonstrable leadership skills in directing the work of others
Problem solving
? Manage a wide range of problems, requiring complex judgments and innovative solutions, needing well-developed conceptual thinking and thus having a high level of business risk management
? Access external resources for advice and respond to external events by adjusting plans or developing new approaches to working
Leadership Capabilities:
? Passion for Customers
? Thinks Strategically
? Acts Decisively
? Drives Performance
? Works Collaboratively
? Develops People and Organization
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Hepatic |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in hepatology
· MD background with strong expertise in hepatology, ideally drug-induced liver injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Renal |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in nephrology
· MD background with strong expertise in nephrology, ideally drug-induced kidney injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| Manager Clinical Affairs |
| A minimum of a Bachelor's degree is required with a minimum of 8+ years of experience in the Clinical Research of medical devices or pharmaceuticals, or 12+ years equivalent work experience in the Clinical Research of medical devices or pharmaceuticals. Pharmaceutical specific experience is preferred. A degree in a science related discipline is preferred. Supervisory responsibilities or experience is an asset. Complete understanding and application of principles, concepts and practices of clinical research procedures will be required. Knowledge and experience with Good Clinical Practice (GCP) is required. Experience working with Regulatory Agencies is required. Opthalmic experience is an asset. Strategic and tactical Clinical and Business knowledge to gain approval and ensure maintenance of legal marketing status of all products will be required. Strong communication, organizational and interpersonal skills are needed. Broad based technical knowledge and skills in diverse areas of business (e.g. R&D, Operations, QA, laboratories, marketing, etc.) are an asset. Ability to effectively negotiate and influence peers, affiliates and Regulatory agencies to ensure that regulatory and business needs are met will be needed. Must have flexibility to provide innovative approaches to gain marketing approvals globally. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| R&D Co-Op- Fall 2010 |
| Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer. |
| Johnson & Johnson Family of Companies |
Glendora |
CA |
11/19/2009
|
| TEST LAB SUPERVISOR |
| Education and/or Experience: a Bachelors Degree in Electrical/Mechanical Engineering or related field with a minimum of 5 years industry experience and 3 years medical device experience. It is also required to have System Engineering experience in multi-disciplinary products ( Software and Hardware). Knowledge and experience in development processes and in documentation writing is an asset in this role. Lead, design, develop, and implement test equipment and test specifications is required.Strong knowledge of one or more of the following standards such as ASTM, UL, IEC 60601-1, ISO 8536-4 and ISO 10555-1 & -5 is preferred.Knowledge of GMP and other regulatory requirement is also preferred for this position.OTHER SKILLS and ABILITIES:Test Lab Supervisor will be expected to have strong analytical reasoning with excellent communication skills.Test Lab Supervisor will have the knowledge, skill and ability to provide technical support to project teams.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Branchburg |
NJ |
11/19/2009
|
| MANAGER, DATA MANAGEMENT - Bridgewater, NJ |
| A minimum of a Bachelor's Degree or higher in a Scientific or Medical field is required. A minimum of 6 or more years experience in Clinical Data Management is required (8 or more years experience is strongly preferred). The candidate should have demonstrated data management expertise including EDC development and experience in managing data management tasks across multiple clinical trials. Experience with project management is a plus. The candidate must have the ability to develop and maintain excellent working relationships with regulatory, clinical personnel, and external data management suppliers. Excellent written, oral, communication and organizational skills. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Senior Quality Engineer |
| A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field is required, with an Advanced degree is preferred. A minimum of 4+ years of Quality Engineering experience is required. Experience in the medical device, pharmaceutical or other highly regulated industry is required. New product development experience is required. Supplier quality engineering experience is a plus. Experience with the development of Electro-mechanical devices is an asset. Knowledge of IEC 60601-1 is preferred. Knowledge of ISO and/or cGMP regulations is required. Strong knowledge in Quality Systems Regulations (QSR) preferred. ASQ certifications (CQE, CQM, CRE or CQA) is preferred. Six Sigma Green Belt or Black Belt is desired. Knowledge in Statistics, Sampling Planning, Reliability, Computer System Validation and Process Validation is an asset. Candidate must be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Operations, Purchasing, Marketing and Medical Affairs. This position may require up to 20% travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Quality Engineer - Irwindale, CA |
| A minimum of a Bachelor's degree in Engineering, Physical, Biological, or natural sciences, along with a minimum of 8+ years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required. An MBA, Master's, or advanced degree in an applicable field of study is an asset. An American Society for Quality (ASQ) certification is an asset. Experience or knowledge of Six Sigma, Lean Manufacturing, or Process Excellence tools is desirable. Must have the ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence assessments. Project management experience or skills ensuring fulfillment of new product development requirements is required. Development and implementation of Quality standards applicable to the medical device or other highly regulated industry required. Knowledge of Quality and Operations systems and processes, including GMP, in a regulated industry is required. A knowledge of Quality Systems Regulations (QSR) requirements as they relate to medical devices is required. Auditing experience is an asset. Knowledge of Quality Engineering, design control, and verification and validation (V&V) tools and methodologies required. The ability to effectively communicate with internal and external personnel at all levels of the organization will be needed. Well-developed influencing and negotiation skills and the ability to effectively train and mentor a diverse array of employees at all levels of the organization will be needed. Business and financial acumen an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Due to technical upgrades, this requisition is replacing requisition # 0903032. Any candidates who have already applied to requisition # 0903032 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Warsaw |
IN |
11/19/2009
|
| Quality Engineer II |
| A minimum of a Bachelors Degree, preferably in a technical discipline, or a minimum of 2+ years of Engineering or Quality experience related to this role is required. A minimum of 2+ years experience within a regulated environment is required, or 1+ year experience in a regulated environment with an advanced degree. Experience in an FDA regulated environment is an asset. Process Excellence, ASQ, Lean Manufacturing training and/or certifications are an asset. Process validation and verification activity experience is an asset. Risk analysis techniques, including FMEA (Failure Modes and Effects Analysis) or other methods, is required. Problem solving techniques including root cause analysis and cause and effect analysis are an asset. Statistical techniques and methods are an asset. Blue print reading and interpretation including Geometric Dimensioning and Tolerancing (GD&T) is an asset. Must have strong negotiation skills and the ability to apply good manufacturing/laboratory practices (GMP and GLP). Working knowledge of QSR and ISO 13485 (ISO9001/EN46001) quality system requirements are an asset. Prior project management experience would be preferred. Working knowledge of Microsoft Word and Excel are required, with Access, Project, and PowerPoint knowledge an asset. Excellent written and oral communication skills will be required. The ability to work independently and partner with a cross-functional team is required. The qualified candidate for this hands-on position should be able to use Quality Engineering principles, tools, and practices to develop and optimize systems and processes that are aligned with the overall business and quality vision. Will require the ability to lift up to 25 pounds. This position will require 10-20% travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Due to technical upgrades, this requisition is replacing requisition # 0901213. Any candidates who have already applied to requisition # 0901213 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Clinical Research Associate II (in-house) |
| A minimum of 3 years related CRA experience at medical device or pharmaceutical company required. A minimum of a Bachelors degree is required, preferably in a related field. CRA certification is preferred. Must possess excellent written and verbal skills. Must possess working knowledge of medical terminology and clinical research applications. Ability to interact and work with other departmental personnel and work as a contributing team member. Must be detail-oriented with strong organizational skills. Must have strong basic understanding of research methodology and FDA regulations. Must be able to work independently. Must be innovative, creative and flexible and able to effectively identify and resolve problems. Familiar with MS Office, including Word, Access, Excel and Outlook. Ability to use internet to perform basic research. 40-50% travel is required. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Disposable Products Group Lead (2nd Shift) |
| Minimum of a High school Degree or equivalent required. Minimum 5 years of business experience preferably in Production, Operations, Procurement, Manufacturing, Supply Chain and/or related discipline. Previous experience working in a regulated environment required. This is a second shift position and requires the ability to work second shift (3:30 PM to midnight). This position requires the ability to work overtime (third shift) and weekends as needed. This position is located in Raynham, MA and does not provide relocation assistance or transportation assistance. Ability to read and write English required. Demonstrated leadership qualities required. Ability to effectively communicate and work with all Operators and Production Support Associates required. Proven track record of success is required. Ability to continuously monitor and meet daily quality standards, production metrics and efficiencies while complying with QSR, ISO and Safety regulations is required. Ability to interpret & follow detailed process specifications with no supervision is required. Ability to work in an open work area and in a clean room environment on a daily basis is required. Ability to work well independently and on small or large teams is required. Intermediate to expert level proficiency in Microsoft Office (Outlook, Excel and Word) required. Ability to lift 25 pounds and to stand and sit for extended periods of time is required. Ability to prioritize and coordinate multiple tasks and projects in an environment of competing priorities is required. Previous experience working with MRP or ERP system preferred. Experience managing workflow processes and daily production schedules strongly preferred. Experience working in Medical Device, Disposables and/or Clean Room environment is highly preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| ENGINEER II |
| A minimum of a Bachelors degree in Engineering or an equivalent scientific discipline is required. A minimum of 2+ years of related engineering experience is required. An Advanced degree in a relevant discipline and 3+ years of related engineering experience is preferred. Basic understanding of engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. Knowledge of FDA, cGMP is an asset. Knowledge of PLC, vision (camera), SCADA and HMI systems is required. Experience in manufacturing and quality systems or related applications (OTIS, QERTS, SAP) is strongly preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Proficiency with Microsoft Project is preferred. Excellent verbal and written communication skills are required. Strong analytical/problem solving skills are a must. The ability to work on cross functional teams is required. This position will be based in Rochester, NY in manufacturing operations. |
| Johnson & Johnson Family of Companies |
|
PA |
11/19/2009
|
| Principal Research Scientist (Data Warehouse Administrator) - Radnor |
| A minimum of a PhD is required with at least 5 years of experience. Knowledge of biology and/or clinical science in the therapeutic areas of interest (immunology, oncology, etc.) is required. Must have excellent communication skills, demonstrated leadership skills, and the ability to operate in matrixed and global environment. Technical expertise with bioinformatics and/or medical informatics applications is required. Must have experience with database development in commercial setting as well as experience with data mining algorithms and applying them to biological and/or clinical problems. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Mountain View |
CA |
11/19/2009
|
| Maintenance Mechanic |
| A minimum of a High School diploma or equivalent is required. Technical training in electrical and / or plumbing is required. Technical training in HVAC is preferred. A minimum of 5 years experience performing facility and manufacturing equipment maintenance is required. Experience troubleshooting and repairing in the medical, electronics or food processing industries is preferred. Experience working in a current Good Manufacturing Practice (cGMP) environment utilizing Standard Operating Procedures (SOPs) or Standard Company Procedures (SCPs) is preferred. Basic computer skills required, including Microsoft Word, Excel, PowerPoint and Outlook. Previous usage of Computer Maintenance Management System (CMMS) is required. Experience using CAD and/or Visio is preferred. Knowledge of local and national electrical, plumbing and building codes is required. Very good oral and written communications skills is required. Ability to follow all safety and clean room requirements is required. The physical requirements of this position require heavy lifting (up to 80 lbs). This will be a first shift position between the hours of 6:00 am and 5:00 pm, with overtime, weekend and holidays, as needed by business. This position will require rotating on-call duties for any emergencies or alarms during off hours and weekends. This position will be based in Mountain View, CA. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Mechanic II, Production Maintenance |
| A minimum of a High School diploma, G.E.D. or equivalent required. Technical school preferred. A minimum of 4 years of related equipment maintenance experience and/or training is required. Experience maintaining CNC Mills, Lathes, Grinders, EDMs (Electrical Discharge Machines) and ABB Robotics required. Experience maintaining Fanuc and Siemens CNC controllers preferred. Experience maintaining mechanical, electrical/electronic, hydraulic and pneumatic equipment components required. Basic computer skills required. Must be a certified Forklift and Power Pallet Jack Operator or be willing to become certified. Must be able to supply own hand tools (i.e. screw drivers, socket wrenches, etc.). Must be able to communicate (read, write and speak) effectively in English. Must have strong communication and interpersonal skills. The ability to left heavy loads, stand and/or walk more than 90% of the time and perform twisting and turning activities required. The ability to work in confined or awkward areas, climb ladders and work from heights required. Must have a valid driver's license. Must be a team player and be able to work with minimal technical supervision. Must be able to work 2nd shift (3:30 pm - 12:00 am). This ability to work overtime, including weekends, and to participate in on-call rotation is required. This position requires the incumbent to submit to and pass periodic and random drug testing as a condition of initial and continued employment. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Truck Driver/Distribution Operator |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of a NJ state issued Class B Commercial Drivers License (CDL) is required. Experience operating a vehicle rated 26,000 lbs. or greater is required. A minimum of 3 year of experience driving a truck with CDL accreditation required. Experience in a warehousing operation environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Basic math skills required. Basic computer skills required. Must have excellent communication and interpersonal skills. Must be detail-oriented and demonstrate alertness, accuracy and patience. Must follow good driving procedures and be highly safety conscious. Experience performing basic vehicle service is preferred. The ability to drive and handle a large panel truck on open highways and in congested areas required. The ability to operate a manual and motorized pallet/hand truck required. The ability to lift/carry up to 35 pounds unaided is required. The ability to work occasional overtime is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Maintenance Mechanic (1 of 2) |
| A minimum of a High School diploma is required. Trade school degree preferred. A minimum of 5 years of HVAC, Plumbing and/or Electrical experience is required. Experience as a Maintenance Mechanic in a commercial environment (i.e. manufacturing, industrial) is required. Prior experience in a GMP (Good Manufacturing Practice) or other regulated environment is preferred. Universal EPA certification for refrigerant recovery is required. Experience with CMMS (Computer Maintenance Management Systems) is required. Experience with MP2 is preferred. Basic electrical skills required. Basic computer knowledge is required. Must have excellent communication and practical problem-solving skills. Must have the ability to follow SOPs (Standard Operating Procedures). Knowledge of local and national building codes preferred. The ability to lift and/or move up to 50 pounds is required. Must be a team player and be able to work with minimal technical supervision. Must be able to work a staggered day shift (7:00 a.m. - 3:30 p.m., 11:00 a.m. - 7:30 p.m.), with weekend work and some overtime, requiring rotating on-call duties for any emergencies or alarms during off hours. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Tool Room Technician |
| A minimum of a High school diploma, GED or equivalent required. Vocational, technical or apprenticeship training preferred. A minimum of 3 years of Millwright, HVAC, Pipefitter, Electrician and/or Machinist experience is required. Experience as a Mechanic in a commercial environment (i.e. manufacturing, industrial) is preferred. General maintenance experience preferred. Experience managing a tool crib or parts distribution preferred. Prior experience in a GMP, GLP ISO, QSR or other regulated industry is preferred. Must be a certified Forklift Operator or be willing to become certified. Must possess a current and valid driver's license. The ability to read and understand blueprints is preferred. Knowledge of Microsoft Office (Word, Excel, Outlook) preferred. Experience navigating in a Microsoft Windows environment required. Experience with Material Management software (i.e. CribMaster), Purchasing Systems (i.e. Ariba) and CMMS software (i.e. Maximo) preferred. Must have strong communication and interpersonal skills. Must be a team player and be able to work with minimal technical supervision. The ability to work occasional overtime, weekends and some holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
West Chester |
PA |
11/19/2009
|
| DIRECTOR BILLING & CONTRACT COMPLIANCE |
| BA/BS degree is required, advanced degree is preferred. A minimum of ten years overall business experience with five years in biopharmaceutical, pharmaceutical, or medical device industry is required. Experience working with or familiar with DME Supplier standards is required. Experience working in government/commercial compliance, contracting including but not limited to operational experience in impact analysis and strategic overlays (Pharmaceutical, Device and/or Consumer) and timely/accurate remediation and adjudication, law or related area is required. Experience supervising projects using internal and/or external resources within a matrix environment is required. Demonstrated experience with HCC and GCC programs is required. Health Care Compliance certifications are preferred. This position will be based in West Chester, Pa and will require 15% travel. Due to technical upgrades, this requisition is replacing requisition #0903460. Any candidates who have already applied to requisition #0903460 are already being considered, therefore, you do not need to apply. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Athens |
GA |
11/19/2009
|
| MANAGER, ANALYTICAL SERVICES |
| Minimum requirements include BS/MS with 7+ years of related experience in an Analytical Laboratory; or Ph.D. with 4+ years of related experience in an Analytical Laboratory; or an equivalent combination of education and experience. |
| Johnson & Johnson Family of Companies |
Athens |
GA |
11/19/2009
|
| PROCESS DEVELOPMENT CHEMIST (POST-DOC) |
| Doctoral degree (Ph.D.) in organic chemistry or related field, with 0-2 years of relevant work experience. |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| Engagement Designer - Beauty |
| A Bachelor's degree is required. A minimum of 5 years of Marketing, Media, and/or Communications experience is required. Ability to create connection and experience strategies across variety of disciplines is preferred. Must understand media/communications planning, CRM, direct marketing and integrated communications. Solid qualitative and quantitative analytical skills are preferred. Ability to create communication plans that deliver maximum value is required. Must be adept at balancing brands, agencies, and connection partners to increase number of connection points, to infuse customer and brand insights, and to optimize experience, design, engagement, and success measures. Must be well versed in all touch-points and able to identify required experts to oversee experiences for actionable initiatives. Experience working with research and developing differentiating insights and actions is preferred. Experience working with media companies sales and marketing department is required. Experience working with content creation, branded entertainment, and/or new video delivery models is preferred. Experience managing high level of detail in many disciplines is preferred. Must be a strong communicator, self-starter and strategic focused. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Supplier Quality Engineer I |
| A minimum of a Bachelor's degree is required, preferably in an Engineering, Life Science, or a related discipline. This position will require a minimum of 0-2+ years experience (including internships, co-ops, or other related experience). A Masters/Advanced degree is an asset. Other experience that is an asset, but not required, will include: Experience in a highly regulated industry is an asset. Experience in the Medical Device industry is preferred. Experience in the Pharmaceutical industry is an asset. FDA and ISO regulations knowledge is an asset. Auditing knowledge is an asset. Strong communication, teamwork, and problem solving skills will be needed. Knowledge in root cause analysis skills are an asset. Experience or knowledge with machining manufacturing processes and injection molding an asset. Six Sigma, Lean, or ASQ Certification and trainings an asset. This position will require up to 20% travel. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Maintenance Technician III |
| A minimum of a High School diploma, GED or equivalent degree required. Associate's degree in a technical discipline preferred. Technical school courses and/or previous factory training in Conveyer Systems or building mechanical/electrical/HVAC systems maintenance preferred. A minimum of 5 years of Conveyor Systems maintenance experience required. Experience in the following areas preferred: Programmable Logic Controllers (PLCs), rolling stock (forklift), building mechanical/electrical/HVAC systems. Prior experience in a FDA regulated industry preferred. Packaging machine maintenance experience preferred. Knowledge of maintenance programs and documentation preferred. The ability to work with tools (i.e. hand tools, power tools, etc.) is required. Experience operating a forklift and willingness to become certified as a Forklift Operator required. Must have the ability to follow policies, Standard Operating Procedures (SOPs) and complete work tasks accurately and efficiently. Must have excellent verbal communication skills and demonstrated collaboration skills with team members and management. The ability to lift at least 50 pounds on a repetitive basis, stand and/or walk on concrete floors 90% of the time and bend, twist and perform repetitive tasks are required. The ability to work from heights (i.e. ladders, platforms, and lifts) and under low clearance equipment required. Must be able to work 3rd shift and be available to work other shifts (1st or 2nd). The ability to work overtime, weekends and holidays as needed by business is required. Must be available for rotating on-call duties. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Polish Operator I |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of 1 year of experience working in a machine shop or production line environment, machining precise finished products is required. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to be flexible to change and support change during a Lean process transformation is required. Grinding or buffing experience preferred. Basic mechanical skills required. Experience with routine machine inspection preferred. Experience with measuring devices preferred. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. The ability to work independently and in a team environment is required. Ability to communicate effectively (read, write, and speak) in English is required. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Polish Operator Lead |
| A minimum of a High school diploma, G.E.D. or equivalent required. Vocational designation or training in preferred. A minimum of 3 years of experience working in a machine shop or production line environment, machining precise finished products required. A minimum of 1 year of grinding and/or buffing experience preferred. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Prior experience in a leadership role (i.e. team lead, group lead) preferred. Training experience preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to drive change as a change agent in a Lean environment required. Basic mechanical skills required. Prior inspection experience required. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. Experience collaborating in a team environment required. Ability to communicate effectively (read, write, and speak) in English is required. Must have strong interpersonal skills to work with people of the production floor. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raleigh |
NC |
11/19/2009
|
| Senior Quality Assurance Engineer |
| A minimum of a Bachelor's degree in Engineering, Science, Technology or a related discipline is required, with a minimum of 5+ years experience in a highly regulated industry required, with experience in the medical device or pharmaceutical industry preferred. A minimum of 3+ years experience as a Quality Engineer is required. CQE or equivalent certification is an asset. Experience with Chemical Processing, Chemistry, or in a related lab area is an asset. Thorough understanding of FDA Quality System Regulation, MDD, ISO 13485:2003, quality engineering methodology, and quality management principles are an asset. Working knowledge of Standards applicable to Medical Device Industry are an asset. Experience with medical device product design and manufacturing processes is an asset. Knowledge of statistical tools and techniques is an asset. Experience in analytical problem solving is an asset. Proven accomplishment in Quality System Auditing is an asset. FDA Notified Body experience as a team member is an asset. Personal computer and software applications experience, including e-mail, Internet applications, Word processing, spreadsheet, and database work is required. Statistical Analysis program, Minitab, or other statistics software experience is required. Must be able to work within a team and handle multiple tasks. Experience with dimensional tools (e.g. rulers, optical comparators, calipers, micrometers, pin gauges) and balances/scales is an asset. This position is located in Raleigh, NC. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Preclinical Studies (BetaLogics) |
| M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Must show basic understanding of laboratory techniques associated with work assignments. Schedule experiments in the lab and perform research in a timely, competent manner. Able to independently solve routine problems and develop solutions. Recommend modifications to methodology and understand the impact of those modifications on the broader research area. Able to review, analyze, and interpret data, especially as requires in-depth evaluation of various factors of increasing and/or changing complexity. Prepare technical reports, summaries, written protocols, and analysis. Interact with employees inside and outside of the immediate working group in a collegial, professional manner, sharing information and expertise. Foster communication and collaborative teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. Knowledge of GLP is an asset. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Senior Clinical Budget Analyst - Janssen AI, LLC |
| A Bachelor's Degree is required. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Previous experience with industry benchmarking database(s) is strongly preferred. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong and proven negotiation and problem resolution skills are also required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Experience in assisting and drafting of legal contracts and familiarity of clinical budget development and negotiation is required. |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| Senior Database Administrator (Contract) |
| A minimum of 3 years of experience as MySQL DBA on Unix/Linux on MySQL 4.1 and/or 5.0. Excellent knowledge and experience in InnoDB & MyISAM is required. Experience in DB backup, recovery, replication, High Availability is required. Experience as an Oracle DBA (RMAN, standby server) is nice to have. Excellent skills in SQL and scripting languages (Perl/Python/Unix Shells, etc.) is desired. Nagios or Cacti monitoring work is a plus. This role will require 24/7 pager rotation. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Dir, Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Dallas |
TX |
11/19/2009
|
| Health Systems Manager - Dallas |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| QA Specialist II/III, Computer Validation |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager / Assoc Director, Clinical Supply Operations |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Dir, Regulatory Affairs |
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I, Chemical Engineer |
| - A Ph.D. degree with 1+ years of pharmaceutical industry experience; an MS degree with 3+ years of pharmaceutical industry experience; or a BS degree with 6+ years of pharmaceutical industry experience. Degrees with a life science concentration required, with a preference for concentrations in chemical engineering or chemistry.
- A demonstrated understanding and working knowledge of chemistry and chemical engineering fundamentals; advanced technical knowledge and experience in API process development, process scale-up, troubleshooting, and optimization; applied kinetics, thermodynamics, and transport fundamentals; as well as familiarity with modern laboratory instrumentation (HPLC, GC, FTIR, Raman, FBRM, DSC, TGA, XRPD, etc), automation tools, and laboratory/plant implementation of PAT
- Experience with modeling complex, physicochemical systems; data analysis; statistical design of experiments; QbD concepts, and fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- A track record of successful laboratory and pilot-scale development in the areas of reaction engineering, catalysis, crystallization, separation technologies, drying, and micronization
- The ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
- Experience with the management of external scientific activities and CRO/CMO relationships
- Proven communication (verbal and written) and interpersonal skills
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Manager |
| ?Proven ability to manage teams working on complex tasks
?Proven ability to design and/or execute procedures and communicate those procedures to others
?Demonstrates an in-depth understanding of applicable regulations
?Displays ability to influence within technical area of expertise
?Proven ability to manage projects of moderate scope and complexity
?Exhibits understanding of technical disciplines beyond own specialty area
?Proactively identifies and resolves problems
?Demonstrates strong oral and written communication skills
?B.S. (or equivalent degree) and 6+ years relevant work experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp QA Specialist |
| Bachelor's degree or equivalent in the Sciences. 5-7 years experience.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Financial Systems Analyst |
| Minimum Requirements:
Bachelor?s degree in Computer Science, Engineering, Finance or Accounting and 4+ years of relevant work experience. Leadership attributes and demonstrated ability to work with more senior staff. Demonstrated strong analytical skills; ability to understand, trouble shoot, process map, and efficiently explain complex financial systems. Prior working knowledge of a major ERP (Oracle) and financial planning tool (SAP/Outlooksoft, Cognos, Hyperion) a must. Independent worker with demonstrated ability and willingness to take on new projects and work with teams.
Familiarity or experience with pharmaceutical research and development process a plus, but not required. Flexibility to work in a fast paced and dynamic work environment.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Director, Regulatory Affairs- Agensys, Santa Monica, CA |
| Bachelor?s degree in life sciences, Chemistry, Biology preferred. Advanced degree is a plus. 8-10 years previous biotechnology and/or pharmaceutical drug development experience. 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 regulatory strategy and submissions. A minimum of 5 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA & ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submission and negotiations with the FDA. Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to others in the department as needed. Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members. Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards. Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence direct Agensys staff and colleagues and groups within Astellas global organization. Highest integrity with respect to professional standards and maintenance of proprietary, confidential information. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Associate Director, Pharmacovigilance QA Lead |
| 1. Minimum B.A/B.S. in science (biology, chemistry, pharmacy) or relevant related field of study. 2. Minimum of 5-to-9 years experience in pharmaceutical or biotechnology industries, including safety quality assurance and management experience 3. Ability to work independently and also within teams are essential4. Ability to travel up to 20% domestically and/or internationally 5. Working knowledge of FDA and international regulations (e.g., Volume 9a) 6. Ability to interact and communicate effectively with various levels of management. 7. Excellent communication and project management skills 8. Computer skills to include Microsoft Office (Power Point, Visio, Excel), Access and Project 9. Excellent facilitation, negotiation, problem-solving, and conflict resolution skills 10. Initiates and maintains extensive contacts within both internal and external networks 11. Excellent oral and written communication skills including the ability to present formally and informally within area of expertise to a diverse set of audiences, including senior management and external customers |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Manufacturing Associate II-- 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 |
11/19/2009
|
| Facilities Department Planner/Assistant |
| ? An Associates of Arts degree preferred? A minimum of two years experience working in an 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 |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manufacturing Tech V |
| BS Degree in a related field and 2 - 4 years experience preferred or 10 years or more equivalent work experience. Trackwise, SAP and deviation experience a plus. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Library & Information Access Intern |
| College science background in Biology or Chemistry or Library/Information Science.
- Minimum overall GPA of 3.2
- Full-time matriculating student who has completed sophomore year at an accredited college or university
- Demonstrated leadership skills
- Excellent communication and organization skills
- Strong proficiency with MS Office applications
- Good interpersonal skills a must
- Good attention to detail
- Database, information science or library background a plus, especially cataloging. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002391. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001968. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemist |
| This position requires candidate to be currently enrolled in a BS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002018. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Engineer |
| This position requires candidate to be currently enrolled in a BS program in Mechanical, Industrial, Electrical Engineering or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # ENG002103. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Chemical Engineer |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Chemical Engineer |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001998. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001988. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002401. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| Co-Op, Graphic Designer- Labeling Services |
| This position requires candidate to be currently in pursuit of a minimum of a Bachelor's degree in graphic arts, package design, or related field. Experience in a pharmaceutical, food, cosmetic labeling or packaging design and development group is a plus. Demonstrated proficiency in the Macintosh Operating System and in graphic arts application software (Creative Suite, including Adobe Acrobat/Distiller, InDesign, and Illustrator) required to produce fully-composed, electronic artwork for printed packaging components (labels, cartons, etc.) is required. Candidate must be able to work full time for a minimum of six months. Successful candidate will display accurate and thorough work. Shows good judgment with thought and detail. Effective communication skills (oral and written) as well as strong organizational skills essential. Strong interpersonal skills and the ability to work well with others and provide significant contributions as a member of a team. Demonstrated flexibility and handle multiple tasks well under pressure. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # QUA001917. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003888. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Science Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003932 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003918. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Science Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003942. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Graduate Intern |
| This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| MMD PhD Biology College Recruiting |
| · PhD Biology, Microbiology, Virology· Strong personal character and ethics· Superior Communication and Interpersonal Skills· Excellent Academic Achievement, Analytical Ability· Ability to work effectively with others as well as independently· U.S. citizen or lawful permanent resident of U.S.· Laboratory experience is preferred Opportunities exist in manufacturing areas and include opportunities in process validation and manufacturing technical areas. Opportunities are available in analytical, biological, and vaccine development. Each of these opportunities provides a challenging environment to learn and contribute. The successful candidate will be expected to carry out research on assigned problems in the above listed areas, including applied development, problem solving, process / product improvement and laboratory testing in the above listed areas. Many analytical techniques are used, including both in vivo and in vitro methods, to characterize complex biological products and systems The candidate is expected to work in a team environment and provide all essential understanding toward addressing mechanisms responsible for product safety, efficacy and stability. Responsibilities will also include the analysis and interpretation of data for problem solving and predictive purposes. A company-wide program is available to facilitate individual development planning to prepare the individual for increasing responsibility according to either technical or management tracks support career path planning. This may include movement to other divisions of Merck & Co., Inc. Those who join Merck can look for substantial early responsibility, the opportunity to develop and apply state-of-the-art technologies, chances for growth and advancement in an informal, varied work environment. Specific openings in MMD are as follows:Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA) is responsible for process implementation, validation and maintenance for biological processes. Specific needs are in the Bioanalytical area which is responsible for assay development and support.At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD, we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.If you are the kind of individual who thrives on challenge and possess the technical, leadership and business skills that are of value to our business, we invite you to apply. Please go to www.merck.com/careers and enter your profile and resume for requisition BIO002450 so that we can keep track of you through the whole recruiting process. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Chemical Engineer |
| Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| MMD MS Chemistry College Recruiting |
| QualificationsThis position requires candidate to be currently enrolled in a MS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002122. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001961. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Specialist |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 3 years of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001974. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Carlow |
L* |
11/19/2009
|
| Process Engineer Technical Operations |
| Education Bsc. in Engineering, Science or similar discipline |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering, Materials Engineering/Science or Pharmaceutics with a minimum of 8 years post-bachelors degree experience in Technical Operations, Process Development, or related experience (Ph.D., 4 years or more experience required). Required:At least 3 years of experience in the formulation/development and technology transfer of controlled release dosage forms. Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at both pilot scale and during scale up. Thorough understanding of polymer chemistry and other materials along with their impact on drug release. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENG002042. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Manufacturing Supervisor |
| Educational Requirements:High School or GED Required Experience/Skills:Minimum 3 years of Supervisory experience. Minimum 2 years working experience in cGMP environment. Willingness to work off-shift or weekends. Computer literacy in MS Office, Word, Outlook, Excel. Preferred: Education:B.S. with emphasis in Science or Engineering. Experience:cGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical). Manufacturing plant experience in operational capacity. Experience working within a Union environment. Experience with working in SAP or other Enterprise software. Technical writing experience related to investigations into manufacturing process variation. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000338. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. ZZ5ML |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer |
| Education:· B.S in Engineering, Biological Sciences, Chemistry or Physics. M.S. in Engineering, Biological Sciences, Chemistry or Physics preferred.Required:· Minimum of 4 years work experience required; with 2 years of work experience specifically in the field of validation. Specific experience in at least one of the following areas is required:· Filter performance qualification using Filter Integrity testers, bubble point, and diffusive flow testing. Experience in validation desired; alternatively, experience in engineering or operations is acceptable with use of sterilizing filters, tangential flow filtration, ultra filtration, and vent filters.· Container/ Closure Integrity testing using microbial ingress and helium leak testing. Experience in validation desired; alternatively, experience in engineering or operations using welders, sealers, and aseptic fluid transfers using sterile bags and manifolds is acceptable.· Experience in a GMP or ISO13485 laboratory performing microbiology, environmental monitoring or engineering development work. Support the GVTE / BSV Lab Coordinator, with performing instrument qualification, metrology, SOP development , creating training material, lab notebook review, performance of internal audits (chemical hygiene, safety, 5S, GMP), and carrying out improvements activities and corrective actions in response to audits.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002123. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering or Materials Engineering/Science. Required:A minimum of 8 years post-bachelors degree experience in Manufacturing, Process Development, or acceptable related experience (Ph.D., 4 years or more experience required). Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at various scales (lab/ pilot plant etc). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE001837. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Environmental Services Manager |
| Requirements: Bachelor's required. Concentrations in an environmental discipline highly preferred. Relevant professional certifications and/or Six Sigma Green Belt a plus. Minimum 10 years applied environmental professional work experience in a pharmaceutical, chemical or manufacturing environmental, coupled with 3 years in a position of environmental program leadership. Proficient in federal and state and regulatory programs. Excellent leadership, program management, project management, and organizational skills. Excellent verbal and written communication skills. Excellent interpersonal and negotiation skills. Proficiency in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000114. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Safety and Industrial Hygiene Manager |
| Requirements: Bachelor's degree required. Concentrations in Safety, or Industrial Hygiene strongly preferred. Relevant professional certifications and/or Six Sigma Green belt a plus. Minimum of 10 years applied safety professional work experience in a pharmaceutical, chemical or manufacturing environment, coupled with 3 years in a position of safety program leadership. Excellent leadership, program management, project management, and organizational skills. Demonstrated experience in developing facilities to meet OSHA VPP certification criteria or equivalent. Broad based knowledge of safety regulations. Customer focus-team building, proactive style. Excellent verbal and written communication skills. Proven record interpersonal and negotiation skills. Provenience in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000115.Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Research Fellow (Particle Sizing) |
| Education:PhD required Required:At least 5 years of post-doctoral or industrial experience. Candidate must demonstrate expertise and hands-on experience in the application of biophysical methodologies in characterization of biomolecules. Expertise should include theoretical and working knowledge of light scattering methodologies such as multi-angle light scattering (MALS), and varied spectroscopic techniques (CD, AUC, etc.). Qualified candidate is required to be highly motivated and possessing excellent verbal communication and writing skills. The candidate is expected to maintain a high degree of scientific rigor under all circumstances and be accessible to provide scientific supervision. The candidate must also demonstrate ability to work effectively both independently and in a multidisciplinary team environment. The individual can be expected to represent the department at cross-functional team meetings in support of data or decisions arising thereof. Preferred:Experience in innovative solutions to biological particle manipulation, aggregation source, molecular size determination and stabilization over a wide size range of biologics (proteins to viruses). GLP/GMP experience. Significant pharmaceutical experience. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002487. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Relationship Manager |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 6 years experience in commercial, business, quality, technical or manufacturing operations functions. Must have strong demonstrated interpersonal and communication skills. Must have demonstrated personal networking and relationship building skills. Ability to work independently with all levels of the organization is required. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex). Travel to supplier locations to develop and manage the supplier/Merck relationships is a key enabler of success with this position. The travel expectations are ~ 10% to 25%. Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. A key responsibility of this position is to serve as the primary point of contact for coordination, oversight, problem solving and communication with MMD's suppliers. Must have tangible experiences, either internal or external to Merck, associated with relationship building and networking. Preferred:Technical writing skills, and experience with data management, collection and analysis. A strong knowledge of and broad experience in Quality Assurance. Experience in conducting or participating in atypical process investigations is preferred, as working with suppliers to resolve problems and implement corrective actions using problem solving techniques is a key expectation. Experience developing process flowcharts and using Microsoft Visio. Familiarity with the MMD Quality Management Systems (QMS). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001949. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Data Management Coordinator |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 5 years experience in commercial, business, quality, technical or manufacturing operations functions. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex) Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. Excellent analytical and computer skills, including software packages used in the maintenance and analysis of data. Excellent interpersonal and communications skills. Ability to work independently with all levels of the organization along with strong planning/organization skills. Preferred:Experience using Lean Six Sigma tools, particularly Black Belt or Green Belt certification. Familiarity with the MMD Quality Management Systems (QMS). Experience operating a database to enter, store, retrieve, and trend data and well as document management (e.g. MIDAS, Documentum, Panagon). Experience developing process flowcharts and using Microsoft Visio. Familiarity with Microsoft Project to assist in developing project plans and timelines. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001933. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Site Compliance Specialist |
| Education:A Bachelor of Science in a life science (such as Biology, Chemistry, etc.) or an appropriate Engineering field is required; candidates with majors in other fields will not be considered. A major in Biology, Microbiology, Biochemistry, Virology, or Engineering is preferred. Required:At least two (2) years of experience, in broad based quality control and/or quality assurance audits or inspections, or other experience in a variety of manufacturing, packaging, testing, or technical support areas. Desired:Experience in bulk vaccine manufacturing or other bulk vaccine support area is desirable. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001929. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering5 years experience in a process engineering support or capital project engineering role supporting an FDA regulated processPreferred:Experience with a sterile/aseptic processExperience with a pharmaceutical manufacturing process Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002167. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering 2 years experience in a process engineering support or capital project engineering role supporting an FDA regulated process Preferred:Experience with a sterile/aseptic process Experience with a pharmaceutical manufacturing process Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002165. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op- Sterile Manufacturing |
| This position requires applicants to be pursing degree (BS/MS) in Engineering, Science, or operations based Business degrees (Industrial Engineering or Commerce and Engineering).Grade Point Average (GPA) of at least 3.0 or higher is preferred. Applicants must be available for full-time employment for 6 months with targeted start date in March 2010. Ideal candidate will be currently enrolled in an academic program and returning to school following this assignment. Successful candidate will possess strong interpersonal skills and writing skills, with an attention to detail. Previous experience in the pharmaceutical industry is preferred but is not a requirement. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM004024. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op- Viral Vaccine Engineering Services |
| This position requires applicants to be pursuing degree in Chemical, Mechanical, or related Engineering discipline. A Grade Point Average (GPA) of at least 3.0 is preferred. Candidate must be available for full time employment (40 hours per week) for a period of 6 months targeted to begin in March 2010. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities" create a profile and submit your resume for requisition #ADM004026. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Bio-Process Technician |
| Education: Bachelor degree in Life Science or Engineering OR Associates degree in Life Science or Engineering and 2 years experience working in the FDA regulated industry. Required:Must be able to lift 50 lbs Must be willing to be vaccinated/blood tested for titer for products manufactured within the facility Must be flexible to work different shifts Preferred:Experience in biological and/or vaccine processing preferred Experience performing aseptic/sterile operations Experience with GMP's (Good Manufacturing Practices) Mechanical aptitude and ability to analyze equipment and take appropriate corrective action Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007545 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Co-op Pilot Plant Operations |
| This position requires students to be in their Sophomore, Pre-Junior, or Junior year, pursuing a Bachelors of Science (B.S) in Chemical or Mechanical Engineering. A minimum Grade Point Average (GPA) of 3.0 is preferred. Prior pharmaceutical experience is a plus. This position is based in Rahway, NJ. Candidate must be available for a period of 6 months. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers . to create a profile and submit your resume for requisition # ADM004029. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Coordinator |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000134. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Associate |
| Required:B.S. degree with a technical emphasis in an appropriate scientific or engineering field. At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills. Attention to detail, flexibility and an awareness of production and attendant quality control problems. Preferred:Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000124. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support |
| Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Instrumentation Technician |
| Required:High School Diploma or GED Effective calibration/troubleshooting skills Ability to communicate and work in a highly effective team environment Ability to manage multiple priorities and advance several tasks in parallel Demonstrated mechanical aptitude Operation/use of general hand and power tools, instruments and testing apparatus common to the electronic and instrumentation fields Ability to read P&ID's, electrical drawings, blueprints, PLC ladder logic, etc Asset:Experience in aseptic or GMP/regulated manufacturing environment Ability to work with and troubleshoot computer control equipment, including Programmable Logic Controllers (PLCs) and Distributed Control Systems (DCS) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007495. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Process Chemistry (Ph.D.), temporary mandate 12 months |
| Education and experience: We are looking for a chemist with an Ph. D. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to the discovery process for new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Ideally the candidate will have completed post doctoral studies and have a minimum of 2 years industrial experience.Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000131. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000137. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000141. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000133. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Operations Coach - Cap & Inspect Production Leader |
| Required: Minimum 2 years coaching/supervisory experience. Minimum 4 years experience in a manufacturing role in an FDA regulated environment Bachelor Degree in Engineering or Science field Asset:Manufacturing experience with automated vial capping and/or inspection equipment Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000389. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Production Technician |
| Required: HS Diploma/GED 3 years experience in a manufacturing environment with a responsibility for mechanical troubleshooting and repair of automated equipment. Ability to work in a highly effective team environment Strong communication (written/verbal) skills Ability to manage multiple priorities and advance several tasks in parallel Ability to work with and troubleshoot computer control equipment including Programmable Logic Controllers (PLC) and/or Distributed Control Systems( DCS) Basic computer fluency (internet browsers, e-mail, word processing)Asset:Associate or Bachelor degree in technical field Bioworks certificate Completed coursework in biotechnical field Experience in clean room or GMP/regulated manufacturing environment Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007356. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Project Scientist |
| Education:BS in Biological Sciences Required. MS in Biological Sciences Preferred Required experience: 3 years post-bachelors degree experience in supply for therapeutic proteins/vaccines/biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007555. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Staff Biochemist |
| Education:BS in Biological Sciences Required. Required experience: 1 to 3 years post-bachelors degree experience in analysis and supply of biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007589. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point, United States |
PA |
11/19/2009
|
| Process Engineer |
| Education:BS in chemical/biochemical engineering, pharmaceutical science or chemistry/biology. MS in chemical/biochemical engineering, pharmaceutical science or chemistry/biologyRequired:3 years manufacturing experience in the areas of pharmaceutical process start up and technical transfer or have demonstrated experience in these areas.Must be able to multi-task and work within tight deadlines. This position requires flexibility and the ability to work independently, as well as excellent organizational skills. Strong professional and interpersonal communication skills are also required. Travel will be a requirement of this position at approximately 30% (US, Puerto Rico, and China). Preferred:Experience with packaging operations is desired. The individual should also possess strong business acumen and interpersonal skills.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002152. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Chemistry (BS.c/MS.c level), Temporary position 12 months |
| Education and experience: We are looking for a chemist with an B.Sc /M. Sc. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to discover new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Personal research efforts are also encouraged and applicants should demonstrate interest to contribute to their field. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Engineer/Scientist |
| Education Requirement: BS/MS/PhD in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 6 years relevant experience (May be combination of post-graduate education and/or work-related experience.) Required: Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project leadership. Desired: Both downstream and upstream experience preferred, but in-depth experience in one area acceptable. Prior experience in late stage bulk process development, process validation, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing would be preferred. Working understanding of analytical methods to characterize biologics, US/EU regulatory requirements is a plus; working knowledge of cGMPs is an added benefit. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # SCI003914. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer/Scientist |
| Required:BS / MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 2 (for BS) / 0 (for MS) years relevant experience. Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project work. Desired: Both downstream and upstream experience preferred, but in-depth experience in one area acceptable. Prior experience in late stage bulk process development, process validation, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing is a plus. Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #SCI003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Engineer |
| Education:Bachelor's degree required. The desired educational background is a BS in an appropriate Engineering field, Operations Improvement, or Business Administration. Other fields of study will be considered if accompanied by significant relevant experience. Required:Three or more years of related Industrial, Production, or Staff experience, obtained through post-degree work in one or more of the following areas: Project management, operations support, or process improvement Financial analysis, resource allocation, or budget / profit plan management Capital plans and/or projects Regulatory and/or compendial requirements Preferred:Experience in one or more of the following areas: Facilities / space planning Operations research techniques Vendor relations and/or contract negotiation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA002013. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Analyst |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000149. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Operational Coach- Manufacturing Maintenance Leader |
| Required:Minimum of 6 years experience in a manufacturing maintenance role within a GMP facility. Minimum 4 years coaching/supervisory experience Bachelor degree in Engineering or Science Asset:Vaccine/sterile experience Plant maintenance, project engineering and/or operations experience Computer Maintenance Management System (Maximo) SAP Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000272. Merck is an equal opportunity employer, M/F/D/V proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Gen. Techn.-Sheet Metal Worker |
| Education: High School Diploma or equivalent required. Graduation from a recognized sheet metal trade school, OR the completion of a formal sheet metal worker apprectice program. Requirements: At least three years recent full-time experience as a journeyman sheet metal worker, OR the recent completion of four years' on the job training as part of a formal sheet metal worker apprentice program. Preferred: More than 3 years experience as a Journeyman sheet metal worker Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # USW000188. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Process Engineer |
| Education:B.S. in Chemical Engineering or Biological Sciences plus a minimum of 5 years relevant experience. Preferr M.S./Ph.D. in Chemical Engineering or Biological Sciences with a minimum of 3 years related experience Required:Experience with CIP/SIP/process design Demonstrated leadership and teamwork skills, excellent analytical abilities, established written and verbal communication skills. Experience leading a team Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002132. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, HVAC |
| Education/Experience:
High School Diploma and 2 years of related experience; or Associate?s Degree or technical equivalent and no related experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant - Business |
| Education :BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirements: (1) Expert knowledge of/experience with SAS software. (2) Good understanding of global clinical trials practices, procedures, methodologies.(3) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH) (4) Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards. (5) Intermediate knowledge of office tools. (6) At least 8 years experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry (5 years for MS Statistics/Computer Science graduates) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Sr Scientist II |
| Degree(s) in chemistry or related disciplines. Typically requires minimum education and experience as follows:
Ph.D. with 2-6 years relevant experience, MS with 6+ years or BS with 8+ years.
? Thorough knowledge of chemical principles; Excellent analytical skills; Excellent written and communication skills; Thorough experience in analytical instrumentation, GMPs, and validation of analytical procedures; Should be creative and show initiative. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior CQA Compliance Specialist |
| BA/BS or equivalent.
English (optimally a second universal language preferred).
5+ years clinical/industry/health authority experience with at least 2 years GCP auditing experience.
30-40% travel.
Ability to manage and objectively evaluate compliance issues.
Ability to maintain a moderate degree of independence with respect to decision making and problem solving.
Excellent verbal and written communication skills, team player, interpersonal skills.
Excellent computer skills, including Excel, Word, etc.
Thorough knowledge of the clinical development, clinical research processes and drug registration process/requirements required.
Thorough knowledge of GCP regulations and guidelines as well as in applicable Novartis SOPs/NIPs and Business Practices.
Good knowledge of computer validation and Part 11 requirements.
Previous experience identifying training needs, developing and conducting training programs.
Ability to multi-task and function independently as required.
Ability to operate successfully in various team capacities, including leader and/or active member.
Ability to operate successfully in various cultural environments.
Ability to coach and mentor.
Auditor certification a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SDC Compliance Associate - Quality R&D |
| BS/MS in a science field with 8-10 years experience in the pharmaceutical industry.
o Good knowledge and understanding of all GMP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in the pharmaceutical industry with a strong analytical and/or manufacturing background, some R&D a plus.
o Detail oriented with Quality Assurance background with good problem solving acumen.
o Ability to work effectively in a team environment with great organization skills
o Excellent communication skills
o Critical thinking, process and performance oriented. Constant drive to improve working practices
o Provision of timely and accurate documentation to minimize submission deficiencies
o Proven performance in review of key documents by highlighting areas of deficiencies and aiding in remediation of the documentation.
o Timely follow-up and closure of Deviations, Investigations, Change Controls and CAPAs.
o Initiation of trainings and/or other appropriate measures to enhance quality and compliance within department
o Escalation of issues/alerts as appropriate to Upper Management and proposal of corrective actions |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist - Animal Models Laboratory |
| The preferred candidate will therefore have strong experience in animal experimentation design and execution, drug administration, and small animal surgery. The preferred candidate will have knowledge of mechanisms of drug pharmacology and toxicity and biological approaches to study such mechanisms.
Specific responsibilities include execution of diverse animal experiments. The candidate will help the AM Lab Head plan, interpret and present experimental results. The candidate is expected to work autonomously, requiring minimal guidance on major activities, and to collaborate productively and cooperatively with Laboratory Animal Support (LAS) services. Secondary responsibilities include laboratory maintenance, ordering, oversight of junior technical staff, regular participation to project team meetings as assigned, maintaining orderly and up-to-date laboratory records in accordance with best practices for a GLS-practicing (GLP-like) laboratory.
BA, BS, MS required in life sciences or relevant related field. Medical, surgical, veterinary, or specialized animal experimental training is preferred.
Experience
- In vivo pharmacology.
- Small animal surgery.
- Coordination and cooperation with existing animal study support services and personnel.
- Laboratory Management.
- Molecular & cellular biology skills/techniques.
Technical Ability
- Drug administration to animals, including PO, IV, IP.
- Small animal surgery, such as adoptive cell transfer, vascular dissection, etc.
- Collection of body fluids from living small animals, such as urine and blood.
- Small animal necropsy and tissue collection.
- Molecular and biochemical techniques, such as PCR-based genotyping, qPCR, Western blotting, ELISA, and multiplex immunoassays
- Laboratory maintenance.
- Cost and inventory control at the laboratory level.
- Excellence in data summarization.
Presentation
- Excellent oral and written communication skills. Able to independently summarize role of team, experimental approaches and findings, and potential value.
- Able to present and defend data in lab meetings, as well as during external liasing and project team meetings.
- Able to prepare written reports, for AM, Translational Toxicology, iTox, and external consumption.
Three-five years minimal required years of experience
Rational/Justification: Senior Scientist Technical position essential to support work in the laboratory. Translational Safety Biomarkers and Animal Models (TSBAM) is a new laboratory with a mission to provide innovative, fit-for-purpose animal models for project-driven safety studies. We have hired only the Lab Head of the Animal Models Lab, and lack technical support for delivery of defined objectives. This technical position is prioritized to support the Lab activities aligned with the overall safety strategy, and to move high priority activities forward. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research HSE Risk Manager |
| This position requires 3-5 years experience in health, safety, and environmental risk assessment and management in a biotech/ pharma laboratory environment. The successful candidate should have experience in implementation and maintenance of HSE audit systems, development of tools and programs, and will have conducted periodic audits and follow up for corrective measures.
Bachelor degree in life sciences, chemistry, or other appropriate discipline and ABSA certification as a Certified Biosafety Professional (CBP) or other equivalent certification in Occupational Health and Safety Program is required. Solid verbal and written English communication skills. Fluency in additional languages, such as German or Mandarin would be favorably considered. Demonstrated leadership abilities, as well as the ability to communicate and influence others in a complex, matrixed environment are essential. |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| QC Chemist - Temporary |
| BS/BA in Chemistry or life sciences
? Knowledge of applicable processes, regulations and guidance documents; testing and documentation requirements, equipment use, preventive maintenance and troubleshooting.
? Proven ability to work in a team environment through conflict resolution and negotiations. Excellent written and verbal communication skills.
? Adherence to all health, safety & environment requirements in support of departmental and site HSE goals.
? Works in a safe and efficient manner. |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Project Engineer |
| Minimum Qualifications: Technical Bachelor?s degree, Electrical or Mechanical Engineering degree preferred; at least 3 years project experience; demonstrated ability to manage complex concurrent tasks to completion with minimal supervision.
Knowledge of a technical specialty and/or a general knowledge of industrial or pharmaceutical practices, with pharmaceutical experience preferred. Knowledge of and demonstrated use of project management tools, negotiation techniques, industry accepted construction techniques, statistics, control charting, and process capabilities beneficial.
If you require accommodation under the American's with Disibilities Act to apply for this position, contact (402) 467-8808 for assistance. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal Scientist (GMP Facility Manager/Engineer) |
| Education
Minimum: BS/MS or equivalent with greater than 8 years of experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience.
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist of Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Multi-Skilled Craftworker II |
| ? Previous experience in Pharmaceutical, Packaging, or Manufacturing preferred.
? Minimum 5 years experience troubleshooting equipment malfunctions on electronic, pneumatic, and mechanical systems related to a manufacturing and packaging equipment.
? Experience supporting PLCs, HMIs/SCADAs, printing technologies (laser, inkjet, etc) vision/barcode systems, sensors, computer systems, industrial networks and motors (AC/DC drives, servo systems).
? The ideal candidate must be comfortable in an environment where he/she will be asked to troubleshoot equipment that is foreign to them.
? Comfortable working with and supporting computer based systems.
? Experience with continuous improvement environment (ie Lean, six sigma) a plus.
? Problem solving/critical thinking skills are required for detecting, analyzing, and resolving production problems
? Good interpersonal skills and communication skills are essential.
? Preferred: Two year degree in Automation or Electrical technology or equivalent engineering discipline.
? Certified Mechanic/Technician, Journeyman or an accredited training program certificate or equivalent. |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Mgr R&D QA & Compliance |
| Education: Minimum Bachelor of Science in Pharmacy, Chemistry, or other Scientific Disciplines
Experience:
? At least 8 years experience in the pharmaceutical, consumer health, or medical device industry in the areas of manufacturing, quality and regulatory systems, process development.
? QA and cGMP experience in Pharmaceutical, GMP and regulatory (GxPs) requirements including auditing and inspection against regulatory / quality standards.
? Demonstrated experience in managing multiple projects and deadlines.
? Good communication, planning, and organization skills.
? In depth understanding of pharmaceutical manufacturing, regulatory constraints, validation and product development.
? Excellent analytical, organizational, and problem solving skills.
? Good knowledge of computer systems, i.e. Microsoft, Word, Excel & PowerPoint.
? Demonstrated understanding best pharmaceutical industry practices, cGMPs, and Quality Assurance and Regulatory.
? Team oriented individual with personal commitment to human relations, integrity, giving and receiving constructive feedback, adaptability, diversity and communication. Must be adaptable to a diversified working environment. Experience in third party contract operations is preferred. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Manufacturing Quality Manager |
| ? Bachelor?s Degree (minimum) in Technical Area (Chemical Engineering, Pharmacy, Biology, Chemistry)
? 7+ years experience in Quality Assurance, Quality Control or related technical field.
? Knowledge of contemporary quality systems and processes.
? Knowledge or PC tools including MS Word, Excel, Project or equivalent.
? Strong knowledge of GMP/Regulatory Validation requirements and industry standards.
? Knowledge of contract manufacturers/developers helpful.
? Ability to set priorities and manage multiple tasks.
? Effective interpersonal skills.
? Solid project management skills
? Strong management abilities.
? Excellent communication skills |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, GCP Compliance Quality-R&D |
| Education:
Graduate degree in sciences, MD or PhD preferred
Professional Experience:
o Expert knowledge and understanding of all GCP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in clinical development in an industrial setting
o Demonstrated managerial skills in an international setting, with experience of at least 10 years in Clinical Development/Quality Assurance/Auditing
o Ability to work effectively in a team environment with great organization skills
o Excellent communication, negotiation and leadership skills
o Innovative and critical thinking, process and performance oriented. Constant drive to improve working practice |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager Business Planning |
| ? BS/BA/CPA in Finance or Accounting and MBA strongly preferred
? 3 ? 5 years of directly and progressively responsible experience and demonstrated achievement in financial analysis, with a focus on improving analytical decision making, preferably in the pharmaceutical industry
? Broad understanding of various financial management areas such as financial statement analysis, accounting, budgeting, profitability analysis, costing, consolidated financials
? Excellent knowledge of Excel and Powerpoint with working knowledge of SAP R3, BW, TM1 and Business Warehouse or other data warehousing applications desirable
? Highly motivated self-starter with a willingness to assume responsibility, take ownership for their work and intelligently challenge the status quo
? Possesses a strong sense of urgency to meet deadlines, while maintaining attention to detail and quality of work
? Strong team player than can work effectively in cross-functional teams
? Strong analytical skills with the ability to recognize problems, develop solutions and implement them
? International mindset and ability to work in a multi cultural environment
? Excellent communication skills, both verbally and in writing; ability to relay financial information to non-finance groups and interface with all levels of management |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| IT Application Management |
| -BS Degree in Computer Science or equivalent preferred
-6 years or more experience to include service delivery & management of document/records management systems
-Strong Documentum 6.5 (WebTop, BPM, BPI, DTS/CTS)
-Strong Java background
-Strong Web Application background (Tomcat, JBoss)
-Strong ITIL Service Management
-Medium Project Management
-Scientific background preferred |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| HR Generalist |
| Education/Experience:
Bachelors Degree required Masters Degree in HR preferred.
1 or 2 Internships in a Human Resources generalist capacity required.
Detail orientated and excellent communication skills, strong experience with Lotus Notes, PowerPoint and Microsoft Office required.
Applicant Tracking System and Peoplesoft experience preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Histotechnology Research Scientist (BS/MS) |
| The ideal candidate will have a BS or MS degree in a biological or chemical science discipline plus at least 4 years of histology experience. Strong organizational skills, self-motivation, attention to detail, flexibility, proactive willingness and desire to engage in the laboratory workflow, and an ability to contribute to a team environment are essential. Candidates should have experience working in a fast-paced, high volume, high productivity and quality environment, in either an industry or clinical laboratory. Experience and proficiency with immunohistochemistry methodology and image analysis is strongly preferred. Prior experience in cell biology and/or molecular biology techniques is preferred. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Group Head, Biochemical & Organ Toxicology (Cambridge) |
| We are seeking an experienced scientist and manager to lead a Biochemical & Organ Toxicology group within Investigative Toxicology (Preclinical Safety, Translational Sciences) based in Cambridge, MA. Investigative Toxicology is using non-clinical innovative investigations to discover the mechanisms of target organ toxicity and to prevent and solve pre-clinical and clinical drug safety issues. The candidate will be responsible for the design and set-up of new experimental facilities for 3 laboratories, and the management of staff therein. The candidate will also be responsible for subsequent development, implementation and management of experimental studies. The primary deliverable of these laboratories (Endocrine & Repro-toxicology, Protein & Mitochondrial Toxicology and Biochemical & Cellular Toxicology) will be to facilitate the early identification and characterisation of toxicities during preclinical phases of drug development with a particular focus on Novartis Institute for Biomedical Research (NIBR) disease areas, expertise and technologies in Cambridge. In addition, the candidate will also work closely with Preclinical Safety Project Team Representatives to help assess potential safety liabilities associated with novel drugs and their target(s). The candidate will report to the Global Head of Biochemical and Organ Toxicology and will interact closely with colleagues in other groups as a member of cross-functional and multi-disciplinary teams (including global Investigative Toxicology & Preclinical Safety departments, NIBR and external collaborators). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| Education (minimum/desirable):
? MD required. Advanced knowledge in medical/scientific area required - focus is on the Cardiovascular therapeutic area.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| ? MD required. Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Brand Medical Director |
| Education: MD Required
? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Executive Director, Quality Assurance |
| minimum required travel 60%required.
Education and training: Graduate in Chemistry, Pharmacy, Microbiology or another related science
Excellent oral and written English communication skills. Second language is preferred.
Minimum 10 years board experience in Pharmaceutical industry or a related regulatory industry. Valid operational experience includes production of QA/QC operations, quality management experience, development or other relevant experience working at a regulatory health authority. Broad business awareness.
Expertise in one or more areas: Facilities, CSV, Laboratory, Aseptic manufacturing, Microbiology, Biopharmaceuticals, Pharmacovigilance, etc.
Expertise in Compliance and health authority interactions. Expertise in GxPs, working knowledge of legal, quality engineering concepts, risk management techniques.
Experience working on teams (multiple roles) and projects. Working knowledge of global regulatory requirements required.
Involvement in Industry forums desired. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Director-Global Quality Systems |
| ? Bachelor?s degree in Science, Engineering, Math or related field.
? 15+ years experience in regulated industry; 5+ years in leadership role.
? Technical knowledge of various drug manufacturing process
? Experience in Quality Assurance & Quality Systems management.
? in-depth knowledge of chemical/pharmaceutical processes
? In-depth knowledge of regulatory requirements for GMP (Swissmedic, EMEA, FDA) and other international institutions (e.g., VICH, ISPE, PDA
? In-depth knowledge of Computerized System Validation,Standard industry systems e.g., SAP, Trackwise etc. and computer system operation principles |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| CMC Liaison - Pain - Global Regulatory Affairs |
| Education:
- Minimum BA, BS; Preferred MA, MS, PhD, PharmD in Life Science
- Experience:
5+ (Manager) to 8+ (Senior Manager /Associate Director) years in Regulatory Affairs
- Strong successful experience in driving international regulatory activities (Europe, rest of the world) with respect to CMC filing, variations and management of HAs requests - International exposure
- Multicultural skills - strong communicator and customer oriented |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Campus Building Project Leader |
| Education: Undergraduate degree(s) in engineering, architecture, or project /construction management; Masters a plus. 15+ years of program and project management across multiple sites is required.
The successful candidate will have:
?The ability to effectively interact with the company leadership of a major US or European multinational
?A demonstrated history of leading large building design and construction programs through to at least first year of occupancy on time and meeting all major milestones.
?Success in management of very significant investment projects in the pharmaceutical industry.
?Specific experience in designing and constructing lab and animal facilities.
?Well-accepted team player, skilled in managing, organizing and leading international teams.
?Successful history of working with leading first-tier architects.
?Knowledge of, and ability to negotiate and oversee, local project management and construction companies.
?Familiar with local design and construction regulations.
?Proven ability to be able to interact with key industry and government officials and support regular conversations on project status, pending changes in government (local, state) regulations, etc.
?Reputation for the highest personal ethics and standards of business behavior.
?LEED experience with a focus on total cost of ownership.
?Excellent written and oral communication skills in English required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Associate Director, Aggregate Spend/State Law (Ethics & Compliance) |
| ? Bachelor?s Degree in technology or business related field.
? 5 - 10 years of responsibility in business processes, data management, business analysis, or project management capacity.
? Candidate must have a strong detail orientation and focus on quality work product due to the complex and sensitive need for data integrity.
? Candidate should be able to demonstrate solid knowledge of technology solutions and systems.
? Strong communication (written and verbal) and presentation skills required; Ability to interact with multiple cross functional teams at all management levels (IT, sales force compliance, meeting solutions, etc).
? Possess an understanding of business processes and ability to understand end to end processes.
? Must be able to meet project deadlines.
? Excellent organization and database skills are required.
? Demonstrate flexibility and willingness to approach and take on new tasks.
? Candidate must be able to understand and be responsible for appropriate management of sensitive, private, confidential, compliance data. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| ASSOCIATE BRAND MANAGER |
| ? Bachelors degree; MBA preferred
? 1-3 years total brand experience. Consumer Package Goods experience preferred
? Experience in working with and managing agencies, media planning, developing future brand plans, managing budgets, conducting business and market place analysis and developing creative briefs.
? Demonstrative strategic and creative problem solving skills, strong analytical skills, leadership skills particularly of cross-functional teams, oral and written skills and proactive self-starter.
? Broad understanding of brand management principles
? Knowledge of sales and marketing techniques, market research data sources and applications is required
? Outstanding interpersonal skills, with emphasis on ability to influence others in all functions and at all levels in the organization.
? Well-developed oral, written, and analytical skills
? Proficient with Word, Excel, PowerPoint, Lotus Notes |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| ASSISTANT BRAND MANAGER 2010 |
| This opportunity is limited to current 2nd year MBA students only.
? Demonstrative strategic and creative problem solving skills
? Strong analytical and leadership skills particularly of cross-functional teams
? Excellent oral and written skills and proactive self-starter.
? Broad understanding of brand management principles. Knowledge of sales and marketing principles and awareness of market research methods
? Computer efficiency required (Word, Excel, PowerPoint, Lotus notes preferred).
? Ability to analyze and summarize marketplace dynamics.
? Internship with consumer packaged goods company or prior marketing experience a plus |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Analyst, LIMS Technical Support |
| Education/Experience:
High School Diploma and 2 years of related experience. |
| Biogen Idec, Inc. |
San Diego |
CA |
11/20/2009
|
| Associate Scientist II, Molecular Discovery |
1 to 5 years laboratory experience.
A solid understanding of the fundamentals/theory of chromatography.
Excellent written and oral communication skills.
Good computer skills.
Experience with FPLC and/or preparative HPLC a plus. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Director, Discovery & Preclinical IT |
â?˘ In-depth knowledge of informatics and IT solutions in the discovery and preclinical space.
â?˘ Proven expertise in global solutions design, development, and production implementation.
â?˘ Excellent managerial and operational skills, combined with strong customer focus.
â?˘ Ability to effectively communicate with peers, upper management, and business partners
â?˘ Demonstrated ability to articulate and â??sellâ?ť a vision for IT-enabled drug discovery.
â?˘ Proven ability to lead multi-disciplinary, cross-cultural project teams.
â?˘ Comfortable working in a matrix organization and managing by influence.
â?˘ Previous managerial experience in a similar industrial position preferred.
â?˘ Demonstrated ability to forge academic and commercial collaborations is a strong plus. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate II, Quality Control - Virology |
At least 5 years of related experience or equivalent combination of education and experience, previous Quality Control and GLP experience required. Viral clearance/vaccine production experience strongly preferred. Will consider candidates without virology experience if other technical requirements are met (PCR, bioassay, cell culture, etc.)
BS in a Biological Science or related technical field. |
| Biogen Idec, Inc. |
Cambridge |
NC |
11/20/2009
|
| Sr Clinical Logistics Analyst |
- Strong written and oral communication skills
- Ability to multitask on a daily basis and maintain multiple projects in parallel
- Proven capability to work in a fast paced dynamic environment
- Experience in a regulated industry or in an environment dealing with workflow industry contraints (i.e. ISO, ISTA, GMP, etc.)
- Prior Logistics experience
- Cold chain logistics or pharmaceutical logistics experience a plus
Education:
A Bachelor Degree in a technical discipline or Industrial Engineering is required. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Technician II, Animal Care |
â?˘ Minimum of 2-5 years directly related experience.
â?˘ AALAS certification is preferred or successful achievement of certification within 18 months of hire.
â?˘ Proficiency with basic technical procedures and identification methods.
â?˘ Good working knowledge of Microsoft Word and Excel.
â?˘ Strong organizational skills and attention to detail.
â?˘ Strong written and verbal English communication skills. Ability to follow written and verbal instructions.
â?˘ Ability to stand for extended periods of time.
â?˘ Ability to regularly lift/push, or pull up to 50 pounds.
Other
Regular work schedule is 40 hours per week; however, the incumbent may be required to work on weekends and holidays on a rotating basis. This position is over time eligible. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Sr Manager, R&D Application Support & Training |
ď?§ Proven expertise in the management of scientific software support design, testing, production implementation, and training in a large corporate environment.
ď?§ At least 5 years of software management experience is required, with a minimum of 3-5 years of project management experience.
ď?§ Ability to effectively communicate with customers is essential.
ď?§ Excellent managerial and communication skills combined with proven ability to interact in multi-disciplinary cross-cultural project teams.
ď?§ Experience in a similar position in the biotechnology or pharmaceutical industries is preferred. |
| Biogen Idec, Inc. |
Seattle |
WA |
11/20/2009
|
| Senior Program Officer - Agricultural Development |
• Minimum of ten years experience in the development and management of projects involving crop improvement, crop management, extension research and/or seed systems for Africa or South Asia
• A PhD or other advanced degree in a discipline relevant to crop improvement, including plant breeding, molecular marker applications, agronomy or a closely related field
• The capacity to think through, evaluate, justify, and make major investments in agricultural research and development
• An outstanding record of achievement and leadership in the field
• Experience developing, managing, and implementing project strategies and the negotiation, execution, conduct and management of performance-based contracts
• Experience with grants or cooperative agreements
• Ability to think/work at scale as well as “work in white space,” create new ideas, strategize with passionate commitment to a successful outcome
• Demonstrated excellent written and oral communication skills in positions requiring communication with a broad and diverse audience
• Ability to prioritize, focus, and achieve results in a fast paced environment
• Track record of working well with others in teams; sense of humor
• Selfless dedication to the mission, flexibility, and willingness to learn
• Overseas experience and the ability to travel internationally |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Supervisor, Animal Facility |
â?˘Minimum of six to eight years directly related laboratory animal experience with at least three years supervisory experience
â?˘Certification/Licensure: AALAS certification at the LATG level, and CVT certification is preferred
â?˘Knowledge and experience of animal husbandry and sanitization requirements, and cagewash operations
â?˘Knowledge and experience in proper methods of small laboratory animal husbandry, handling and restraint, injection and sample collection techniques and euthanasia procedures
â?˘Advanced understanding of colony health status requirements and applicable animal care regulations
â?˘Excellent interpersonal, supervisory, and leadership skills. Demonstrated ability to interact professionally with investigators, contractors, vendors, and staff
â?˘Sound judgment and decision making skills, effective written and verbal communication and supervision skills
â?˘Excellent organizational and observational skills
â?˘Ability to work independently with minimal supervision
â?˘Advanced working knowledge of Microsoft Word and Excel
â?˘Ability to lift, push/pull 50 pounds |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Associate Director, Supply Chain Quality- Small Molecule |
-Minimum of 10 years Small Molecule experience, with at least 5 years experience in Quality Assurance.
-Understanding of cGMPs, quality systems and regulations.
-Excellent written and verbal communication skills.
Minimum of B.S. in Science or Engineering. Advanced degree preferred. |
| Teva Pharmaceuticals USA |
Fairfield |
NJ |
11/20/2009
|
| Security Officer |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| HR Analyst |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Sr. Manager, Network Administration & IT Security |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Talent Development Specialist |
|
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Manager |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of five (5) yearsâ?? experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- Willingness and ability to travel as required (typically requires 50% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa/Asia medical settings is desired;
- End-user computer efficiency, with proficiency in Microsoft Office products.
Knowledge, Skills, and Abilities
- Demonstrated poise and maturity in communicating with high-level executives;
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks;
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment;
- Strong written and verbal communication skills; must be able to communicate effectively;
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work;
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Laboratory Monitor |
| Education/Experience
- Minimum of a Biotechnology degree or equivalent;
- Minimum of 3 yearsâ?? experience in clinical research and laboratory setting will be a preference;
- Good knowledge of Good Laboratory Practice (GCP) will be a preference;
- Experience working in an accredited laboratory;
- Experience in SOP writing;
- Willingness and ability to travel as required (typically requires 60% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa medical settings is desired.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work.
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
Terms and ConditionsThis position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. International travel required (60%). |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Online Sales Specialist - Intern |
| Completion of sophomore/junior/senior year towards a BA/BS in Chemistry, Biochemistry, or related science degree
Would also consider Business, Marketing or similar discipline
Proficiency in the use of Microsoft Office - Excel, Word, Outlook
Strong interest in interacting directly with customers (via phone, email)
Excellent verbal, written and phone communications skills
Must be a team player with ability to work in a fast paced, dynamic team environment |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| R&D Engineer, Software |
| ? University degree in Electrical Engineering (MS level) required, PhD. in the EM simulation area highly preferred.
? Thorough understanding of EM simulation techniques, particularly in time domain methods, as well as their software implementation aspects, including the implementation of complex numerical algorithms.
? Good understanding on the application areas of EM simulation products.
? Experience in numerical/scientific programming in C/C++ and generally good software development skills
? The ability to work in a multi-site, multi-cultural team environment |
| Agilent Technologies, Inc. US |
Boulder |
CO |
11/20/2009
|
| Quality Control Analyst |
| This is a solutions oriented environment where your energy, enthusiasm and pro-active approach will not only help drive Agilent's continued growth and development, but also your own career success.
EDUCATION and/or EXPERIENCE
Bachelor's degree (B.S.) or equivalent in chemistry or related life sciences field; and five to ten years related experience and/or training; or equivalent combination of education and experience. Five to ten years experience working in a GMP production environment is required.
1. Knowledge of GMP guidelines as well as international regulations pertaining to the production of APIs and drug products.
2. Knowledge and understanding of the oligonucleotide manufacturing or related pharmaceutical manufacturing processes.
3. Skill in communication, written and verbal; will be handling various relations issues and will be confronted with various interactions
4. Knowledge of and skill in using computer software and hardware applications, including Microsoft products and the Internet.
5. Skill in managing various projects; must be able to use individual discretion in completing work assignments; while assisting the group in establishing priorities, setting standards and working collectively to accomplish deadlines and objectives
6. Ability to read, analyze, and interpret industry related periodicals, SOPs, and government regulations. Ability to write reports, business correspondence, and procedures. Ability to respond to common inquiries or complaints from customers, co-workers, subordinates, and supervisors regarding the products and processes.
Geo Location: Boulder CO
cb~11/11/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Regional Government Security Manager (West) |
| - MUST currently hold a SCI level security clearance with a current Single Scope Background Investigation (SSBI).
- Must have a firm understanding of the security policies, procedures and directive of the DoD, National Industrial Security Program and Intelligence Community SCI security programs.
- Bachelors Degree in Criminal Justice, Security Management, Industrial Security, Business Management or equivalent combination of education and experience.
- 5 to 10 years of experience in the Government Security Field.
- Knowledgeable in the use of JPAS, DIAS COMSEC and DoD/OPM Electronic Personnel Security Questionnaire software packages.
- Proficiency with Microsoft Office products is essential.
- Requires the ability to make sound decisions, manage time, take independent action, analyze problems and provide focused solutions.
- Demonstrated ability to effectively communicate information to various audiences and all levels of the organization both verbally and through written communications.
- Must be highly organized, be willing to work in a team environment, be able to prioritize tasking, perform in a multi-tasked and dynamic environment.
- Must be dependable, responsive, customer focused and possess the qualities of diplomacy, tact, excellent judgment, discretion and initiative.
~cb~10/05/09 |
| Agilent Technologies, Inc. US |
Schaumburg |
IL |
11/20/2009
|
| Service Technical Specialist |
| Requires higher education or specialized training/certification.
Requires a minimum of 5 years directly related calibration/repair experience, with typically 7 to 10 years experience. Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment. Experience using automated calibration software platforms (STE, PC Based, Metcal, TME etc) required.
Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Marketing Technical Writer Intern |
| Qualifications:
- Proficient with Microsoft Word and and PowerPoint
- Strong verbal and technical writing skills.
- Strong typing skills
- Proficient and comfortable using internet and web-based tools.
cb~11/03/2009 |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| Semiconductor Fab Integration Engineer |
| M.S. or Ph.D. in Electrical Engineering, Physics, Materials Science, Mechanical Engineering, Chemical Engineering or equivalent experience.
Experience with advanced semiconductor and/or MEMS processes and devices is essential and specific skills in III-V device physics and processing are highly desirable.
Experience with statistical process control and design of experiments is desired.
Candidates should have excellent interpersonal, problem solving, and communication skills for successful inter-group and intra-group interactions.
US Citizenship/Permanent Resident status is recommended, but applications from highly qualified candidates requiring work sponsorship will also be considered.
Candidates requiring work sponsorship must be eligible for access to export controlled electronics technology.
Geo Location: Santa Rosa, CA
~cb~11/02/09 |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Senior System Engineer |
| Qualifications:
?BS/MS in EE or Computer Science and 5+ years of demonstrated experience in architecting and implementing complex solutions for Telco and/or IP Networks.
?Experience in design and/or support using OSI model and current evolutionary trends in Telecoms and IP networks.
?Administration of Operating Systems: Linux and UNIX with working knowledge of Perl and Shell Scripting.
?A broad telecom background and IP technology expertise is essential including UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Ability to develop written proposals and participate in the creation of RFI/RFP responses.
?Strong interpersonal/relationship skills with superior verbal and written communication to effectively communicate with the customer, executives and team-members.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance is also required.Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| System Engineering Specialist |
| Qualifications:
?Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in Mobile Communication Systems and Networks (including cell phone and other mobile communications infrastructure).
?Knowledge of UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Experience with Perl and Shell Scripting as well as administration of Operating Systems: Linux and UNIX.
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance.
Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Customer Account Specialist |
| ? Bachelor of Arts or Bachelor of Science degree
? Ability to travel
? Relevant customer experience
Geo Location: Wilmington, DE
~cb~11/11/09 |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : As the Field Technical Support Representative for a high tech growth business serving the Chemical Analysis and Life Science markets, your primary responsibilities will include: Installation, repair and qualification services for Agilent and non-Agilent analytical instruments (LC/GC/MS) products for customers, on-site. Provides service in accordance to a maintenance contract, which may involve a managed service arrangement. Will be part of a team that delivers services on-site for large volume customers.
Perform the duties of a Customer Service Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Fishkill |
NY |
11/20/2009
|
| Field Service Technical Engineer--Account Management- NJ |
| Description : As the Field Service Engineer for a high tech growth business serving the Life Sciences markets, your primary responsibilities will include: account management, as well as, providing support on analytical LC, GC and MS products for customers, on-site. This role will provide you with the opportunity to join the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies.
Agilent Field Service Engineers deliver technical expertise to customers based on Agilent products and services primarily in the MS area. As an individual contributor, this job will focus primarily on large account management by providing customers with high quality services to ensure customer satisfaction. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and validation services. Other responsibilities include, adherence to environmental health and safety guidelines, understanding our customers business, parts management, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. We are looking for enthusiastic individuals who want to grow with our company and become part of a dedicated group of individuals.
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
11/20/2009
|
| Manufacturing Associate-Intermediate |
| This position requires a BS/BA degree in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology and/or biochemistry. A strong working knowledge of standard laboratory techniques of molecular biology is required ( PCR, DNA and RNA isolation, bacterial transformations). Strong oral and written communication, organization, team building and computer skills essential.
cb~11/11/2009 |
| Agilent Technologies, Inc. US |
San Diego |
CA |
11/20/2009
|
| Field Service Technician |
| Qualifications: Associates Degree in Electronics or recent Military experience/training in electronic measurement calibration and a minimum of 2 years field experience.
Position requires:
? Hands-on Experience as Field Service Engineer or Maintenance Technician
? Knowledge of the calibration and repair of all types of electronic equipment
? Excellent communication skills (customer interface skills)
? Strong organizational skills
? Positive/Energetic attitude
? Willingness to learn |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. Will be part of a team that delivers on-site services at a major account.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/17/09 |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Automation Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Bioanalytical Chemist |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Biochemist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Clinical Data Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| E-Business Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Electromechanical Technician 1st shift |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Engineering Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Facilities Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Facilities Maintenance Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Kansas City |
MO |
11/20/2009
|
| Field Sales Consultant - Acute Care - Kansas City |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Global Business Systems Analyst -Manufacturing Execution System Implementation |
| See above |
| BD (Becton, Dickinson and Company) |
Billerica |
MA |
11/20/2009
|
| Human Resources Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Information Technology Senior Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Inspection Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Instrumentation Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Laboratory Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Business Unit Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Luer Forming Set-Up Operator A Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Luer Forming Set-Up Operator B Shift |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Maintenance Technician III-IV |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Manufacturing Integrator, Diabetes Care |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Manufacturing Technician - Production |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician II (Packaging) |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Microbiologist |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Moldmaker |
| See above |
| BD (Becton, Dickinson and Company) |
Teterboro |
NJ |
11/20/2009
|
| Pilot/Aircraft Captain Corporate Flight Department |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| PosiFlush Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer, Environmental Packaging |
| See above |
| BD (Becton, Dickinson and Company) |
Canaan |
CT |
11/20/2009
|
| Process Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager, Scientific Services |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator I |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator II |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Production Operator IV |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Project Engineer - Packaging |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Project Manager, IT |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Control Microbiologist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Systems Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Regulatory Compliance Complaint Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Research Associate (IVD strongly preferred) |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Trial Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Packaging Technology, BD Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Quality Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Marketing Manager, Strategic Marketing |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Product Manager - Vaccines |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Assembly |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Quality Engineer, Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Software Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Sr. Electro-Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr. Manufacturing Equipment Engineer - Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Sr. Packaging Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Staff Engineer, Packaging Technology |
| See above |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Summer Engineering Internship |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Support Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Tech Transfer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member- ADVANCED MOLDING SKILLS |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Validation Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Technician II |
| See above |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Associate Director, Aseptic Fill Finish Operations |
| Knowledge/Skills/Abilities Required
Strong knowledge of aseptic manufacturing of biologics as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal antibody based therapies required.
Minimum 8 years of relevant aseptic manufacturing experience with biologics, several of which must be in a management position required. Graduate level degree in biological sciences or related subject highly preferred. Individuals without a graduate degree but more experience will be considered.
Prior contract manufacturing project management experience is highly preferred. Prior experience with manufacturing from pre-IND through phase 3 or commercial production is highly desired.
An understanding of project accounting and financial concepts required.
A hands-on, proactive stance is essential with willingness and ability to assist all team members to achieve corporate goals required.
Up to 20% domestic and international travel required. |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Manufacturing Manager |
|
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Manufacturing Manager
Location: Newark-Pencader
Job Code: 51
# of openings: 1
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Description
The Manufacturing Manager is responsible for planning, organizing, staffing directing and controlling production. The manager sets priorities, coordinates the scientists and operators work schedules to meet production requirements while maintaining a high quality standard. Leads continuous improvement programs to increase yield and reduce variation. Helps lead technical troubleshooting and root cause analysis efforts to reduce cost and improve output quality. The manager is an integral part of internal product/process redesigns, new product transfers from R&D and the integration and process transfer of external product/process acquisitions.
Responsibilities and Duties:
1. Manages and coordinates the Scientist/Operator production activities and schedules. Meets job schedules with acceptable quality.
2. Hires new employees and is responsible for operator training & certification, establishes standards of performance, conducts employee performance appraisals and on going coaching. Conducts corrective actions when disciplinary action is required and enforces company policies, rules and regulations.
3. Must be able to achieve completion of objectives through mentoring and coaching others..onitors and measures the department performance, strives for continual improvements in productivity and ways to increase capacity and reduce cost.
4. Monitors and measures the department performance, strives for continual improvements in efficiencies and reductions in variation and costs.
5. Takes ownership for the quality of products produced and services performed.
6. Is dedicated to reducing process variation and champions the use of statistical process control (SPC) and formal problem solving tools across all operations, trains employees in quality theory and practice, writes and modifies procedures to confirm to quality standards and maintains proficiency in problem solving techniques.
7. Responsible for the managing and replenishment of key custome reagents.
8. Responsible for the accuracy of the MRP system data, Bill of Material and Routings, Syspro standards and the material and labor variances.
9. Determines manufacturing capital and tooling needs. Is knowledgeable of the process specifications in his/her area of responsibility and is dedicated to the reduce process variation.
10. Continually works towards control of key equipment variables and process parameters associated with the lyophilizers, fermenters, centrifuges, balances, coating machines, reel-to-reel sprayer and dippers. Ensures equipment maintenance is appropriate and monitored.
11. Writes and follows standard operating procedures and makes certain paperwork is properly filled out and data collection systems reflect accurate product movements.
12. Is knowledgeable of the process specifications in the area of responsibility.
13. Makes sure process changes are documented before a new process or change is implemented on the production floor.
14. Communicates effectively with the Supply Chain Manager and Sales & Marketing to resolve customer performance problems, participates in customer audits and visits.
15. Complies with and aids in the development of department safety rules, monitors area for hazards, uses proper personal protective equipment (PPE) when required and maintains a safe, clean and organized work area.16. Monitors and maintains supplies, spare/contingency parts and WIP minimums to reduce downtime.
16. Performs other duties as assigned.
Qualifications :
BS/BA in biochemisty/microbiology/engineering field
At least 5 years of management experience in a manufacturing enviornment
Familiar with antibody and or immunoassays processes
Good mechanical and mathematical abilities and the ability to make critical judgments within the production processes.
Familiarity with antibody and/or immunoassay processes.
Computer proficiency- Word, Excel, PowerPoint, and Project expertise is preferred.
Knowledgeable of SPC and the use of data driven problem solving tools.
Good verbal and written communication skills.
Abilities:
Consistently meets production schedule deadlines
Consistently sets and meets production goals
Identifies and resolves production issues.
Establishes and makes changes to process for continuous improvement
Trains staff on process
Excellent organizational skills
Must be able to mutli-task
Must be able to apply priority management skills and assess the risk/benefits of decisions and actions.
Supervisory Responsibilities:
Manages a staff of technical and labor personnel. Responsibilities include interviewing, hiring and training new employees, planning, assigning and directing work, conducts employee appraisals, on-going coaching sessions provides a motivating work environment, enforces company policies, rules and regulations and maintains cooperation with other areas.
Work Environment/ Other requirements:
At SDI our work environment varies significantly from job to job. Ability to lift or move 20 pounds and work/travel throughout plant environment of varied temperatures and humidity; grasp and hold small objects, a full range of motion, and to wear personal protective devices. This position may expose the employee to fumes or airborne particles, biohazards, and toxic or caustic chemicals. Daily contact with employees in other departments is required.
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| Miltenyi Biotec Inc. |
|
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11/20/2009
|
| Field Service Engineer: Mid-Atlantic Southeast |
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