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Company Jobs - MedImmune


 

Principal Scientist

Gaithersburg MD

Requirements: experience in successfully managing research project teams and providing scientific and strategic direction at the departmental level. ability and experience in managing junior scientists Has a proven track record of both high quality scientific publications as well as experience presenting at both internal and external scientific meetings. has a proven track record as a team player and should have extensive leadership experience at both the team and departmental level. ability to communicate effectively across all levels of the organization. experience in filing IND's and interacting with the various regulatory agencies preferred but not required. Education: PhD or MD with 10+ years of experience either in an industry (preferred ) or an academic setting. ~BSP *LI-MEDI Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9144 Position CategoryBiosuperiors Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/28/2014 8:34:56 AM

Diabetes Thought Leader

Gaithersburg MD

Minimum Requirements - Education and Experience Relevant advanced scientific or medical degree of appropriate certification (MD and /or PhD preferred) Practical/ working knowledge of the Brand and Disease Area, in this case, Diabetes Demonstrated experience in developing medical strategies and plans Experience with global TL engagement Skills and Capabilities Patient-centred but commercially aware, values driven approach Demonstrated project management skills to lead cross functional teams Ability to translate data into a strategic medical plan Proven ability to engage, influence and build effective relationships with OLs, across functional and geographic boundaries Strong verbal and written communication skills in English Broad understanding of more than one part of the business i.e. Discovery, Clinical, Regulatory, Medical or Commercial roles Presentation and influencing/negotiation skills (essential) High ethical standards required Internal Contacts/Customers * GMA Leadership Team * Global Product Team (GPT) members * The Medical Working Groups (MWGs) -Medical Science Director (MSD) -Global Payer Evidence Directors (GPED) -Key marketing company medical leaders * The Medcial Evidence Center (MEC) -Medical Evidence Directors (MED) and Leaders (MEL) -Global Publications Leaders (GPLs) -ESRO TA Directors * The Global Medical Excellence Team (GME) -Sr Dir MSL Program -Sr Dir Medical Information -Dir Medical Academy -Nom Sig Director -GMQA Leader * In-country Medical Teams * Regional Medical Directors External Contacts/Customers * International/global opinion leaders * Leadership of International Medical Associations * Academic Institutions/Hospitals * Medical opinion leaders in Policy, Payer and HTA environment * Peers in the Industry Reporting Relationship No direct line management/reports Reports directly into the Executive Director, Head of Diabetes Budget responsibility Responsible for the creation, delivery and management of an annual Brand Medical Budget that is aligned with GMD or GPPS budget processes (depending on the life-cycle of the product/brand) Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesSuccessful candidates will be AstraZeneca Employees and will be located at AstraZeneca's MedImmune strategic science center in Gaithersburg, Maryland. MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines. MedImmune is pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines. ~BSP *LI-Medi Req IDS144 Position CategoryResearch and Non-Clinical Development Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

Manager, Strategic Sourcing

Gaithersburg MD

above. Req ID9148 Position CategoryOperations - Supply Chain & Strategic Sourcing Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

Medical Director (Women's Cancer)

Gaithersburg MD

Minimum Requirements: *Graduate of an accredited medical school and recipient of M.D. or D.O. degrees or equivalent *Board certification/eligibility in Oncology (preferred) , internal medicine or a related relevant specialty. *Background in practicing medicine, clinical research, and familiarity with biostatistics, epidemiology and health outcomes. *Excellent written and oral communication, interpersonal, and organization skills. *High level of emotional intelligence. *Strong business acumen, including working knowledge of changing U.S. payer and provider landscape. *Proven ability to interact productively with both commercial and scientific colleagues. *Demonstrated ability to work collaboratively in cross functional teams. *Familiarity with OPDP, PhRMA code, and key regulations in the pharmaceutical industry *Highest level of ethics and integrity. *Ability to travel nationally and internationally. Travel will be up to ~30% of time. *Medical Directors will have at least 3 years of pharmaceutical industry or other related areas of experience . Preferred Background: *Additional training such as an M.P.H., M.B.A. or other advanced degree. *Knowledge of relevant Professional Societies and Scientific Medical Experts. *Experience with pharmaceutical drug development and Medical/Scientific Affairs *Active medical license. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesSuccessful candidates will be AstraZeneca Employees and will be located at AstraZeneca's MedImmune strategic science center in Gaithersburg, Maryland. MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines. MedImmune is pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines. ~BSP *LI-Medi Req IDS145 Position CategoryMedical & Scientific Affairs Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

QA Specialist III - 70011901

Louisville KY

Requirements: Minimum of 4 years' experience in the Biopharmaceutical/pharmaceutical industry. Minimum of four years' experience in quality assurance, quality control or validation. Excellent Communication and interpersonal skills Excellent technical writing skills Ability to adapt to a changing environment and able to set and adjust priorities accordingly Capable of functioning independently with a minimum of supervision/direction Experienced with working in a highly regulated environment (FDA, EMA) Preferred: Working knowledge of Quality Information Systems (e.g., Trackwise) and Enterprise Resource Planning systems (e.g., SAP) Auditing experience Education: * Bachelor's degree is required * Bachelor's degree in biology, chemistry, engineering or other relevant field is preferred. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional Notesn/a Req ID9150 Position CategoryOperations - Quality Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

Senior Clinical Project Manager

Gaithersburg MD

For Both levels we require the following: Education: University degree, preferably in a biologic/scientific discipline Experience and Skills: Thorough understanding of country level regulations, ICH and GCP guidelines Thorough understanding of cross-functional clinical processes including data management, biostatistics, medical writing, drug safety, and regulatory affairs Ability to lead a cross-functional team in a matrix environment Strong interpersonal and negotiation skills Strong verbal and written communications and presentation skills Proven complex problem solving and decision making skills Strong leadership, communication, management and organizational skills, conflict resolution, and team building skills Ability and willingness to travel 25% of the time (internationally and domestically) Provides technical solutions to a range of difficult problems in a program level Works under a minimal level of oversight of AD/D, Clinical Operations Develops approach to solutions and seeks guidance as appropriate In addition to the above, for the CPM we require the following: Minimum of 5 years progressive experience in clinical operations including project coordination, site management and monitoring or equivalent and at least 3 years of project management experience or equivalent Potential to line manage personnel Ability to manage early stage clinical trial(s) and potentially large/global clinical trials with low to moderate complexity In addition to the above, for the Sr. CPM we require the following: Minimum of 10 years progressive experience in clinical operations including 5 years of clinical project management or equivalent. Strong line management experience Experience managing clinical program(s) *LI-MEDI ~BSP Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9141 Position CategoryClinical Operations Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

Sr. Clinical Project Manager/Clinical Project Manager

Gaithersburg MD

Required Education: University degree, preferably in a biologic/scientific discipline. Advanced degree is preferred. Certification or Degree in Project Management is a plus. Required Experience and Skills: At least ten years of experience in the pharmaceutical/biotech industry. Extensive and proven experience in driving operational delivery to timelines, cost and quality Proven experience leading delivery through collaboration with internal organization and external providers Significant experience and expertise in Clinical Trial methodology with a proven ability to deliver differentiated options based on a sound knowledge of operational delivery Proven ability in proactive problem solving and risk management that is solution focused Proven Global Project Management experience with expertise in program level resource and budget management Preferred program level experience across the product life cycle and across multiple therapeutic areas, with experience in global drug development Experience and strength in working and leading in matrix teams Requires minimal guidance and oversight from the Director/Sr. Director, Clinical Operations and/or Sr. Director, Clinical Development or TA VP Strategic Skills including a high level of creativity, innovation, and problem solving with an ability to manage effectively through ambiguity Strong collaborative communications skills including the ability to engage with a diverse client base and manage through conflict Manages the Clinical Operations remit within the PDT and/or GPT structure Ability/willingness to lead strategic and/or operational management of individual clinical trials should the need arise Ability to motivate team members and build cross functional teams in support of the PDT/GPT vision Provide strong leadership and facilitation skills to link strategic direction to a clear operation plan The appropriate candidate must: Act decisively Work collaboratively Exhibit passion for customers Drive performance Think strategically Develop people and organization Possess positive change management skills, at all levels including individually, team and the business, seeing change as an opportunity to improve performance and add value to the business Have a willingness to travel both domestically and internationally Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9142 Position CategoryClinical Operations Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/26/2014 7:27:59 AM

LSI Standards Senior Specialist

Gaithersburg MD

Educational Qualifications Bachelor's Degree required, life sciences, scientific, pharmaceutical or business discipline is preferred. Experience v Experience developing and managing Standards in a global GXP environment. v Experience managing systems and data associated with training/compliance documentation including standardized metrics reports. Technical/Specialized Skills v Excellent interpersonal, verbal and written communication skills. v Medium-to-strong knowledge of FDA/MHRA regulations and guidelines, ICH Guidelines, EU Directives, and overall GCP, GLP, or GPvP is advantageous. v Excellent Project Management, Time Management, and Organizational skills v Excellent PC skills utilizing Microsoft Office products (e.g., Word, Excel, PowerPoint), and basic-to-expert knowledge in one or more collaborative tools (e.g., WebEx, SharePoint). Behavioral Competencies v Ability to work globally, in a highly matrixed environment, spreading across MedImmune and AstraZeneca. v Recognizes responsibility to service customer's needs in a fast-paced, changing environment. v Ability to prioritize effectively and to adapt to changing priorities. v Ability to deal with change and ambiguity. v Team Lead on complex projects with minimal supervisory support. v Ability to influence decisions with customers and stakeholders, ensuring decisions are long-lasting. v Demonstrated project management skills, planning schedules and arranging own activities in accomplishing objectives. v Ability to solve complex problems requiring expert skills and regular use of ingenuity and innovation. v Comfortable interacting with senior stakeholders and managing conflict? *LI-MEDI *NS-Medi Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesPlease note this position is based in Cambridge, uk. Req ID9135 Position CategoryTraining Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/25/2014 7:33:40 AM

Scientist I/II

Frederick MD

Position: - Coordinate and perform process characterization studies, and participate in multiple simultaneous projects that are complex and technically demanding within a specific area/field. - Initiate, implement, plan, direct, and execute investigations to resolve issues, understand process trends, and/or improve process performance. - Support scale-up and technology transfer of clinical or commercial processes to manufacturing facilities, engage in process performance monitoring, recommend/implement process improvement strategies, and develop/qualify process scale-down models. - Responsible for routine experimental planning, execution, and a longer term project or investigations. -Work under general supervision of the manager. -Make detailed observations, analyze data, interpret results and write protocols / reports. Demonstrates scientific rigor in assessing own data and that of others. - Serve as a subject matter expert in cell culture processing and engineering; support implementation of disposable cell culture technology, responsible for developing bioreactor characterization methodologies and data acquisition tool for process monitoring /control. - Able to perform statistical analysis using statistical tool such as JMP, Design Expert, etc.; good knowledge of statistical design of experiments (DOE) and data analysis. - Able to establish effective working relationships toward goals within and outside the department, and support/participate in collaborative projects, where appropriate. -Effectively present results at internal meetings, and participate / present at external scientific meetings. - Responsible for meeting project goals within time and budget constraints. - Applies a working knowledge of related scientific and engineering disciplines including downstream processing/purification and analytical methods. Education: Advanced degree (MS/PhD) in Bio/chemical engineering or biochemistry/biological sciences preferred. Bachelor's degree required at minimum. Experience: For Scientist I - PhD: 0-3 years experience. Masters: 8+ years experience. Bachelors: 10+ years of experience. For Scientist II - PhD: 3+ years experience. Masters: 10+ years experience. BS: 13+ years experience.. *LI-MEDI Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesExperience with bioreactor scale-down model development / qualification and mammalian cell culture process improvement studies. Experience with disposable cell culture technology. Experience with data acquisition for process monitoring /control. Experience with mixing and bioreactor characterization methodologies. Experience with BLA / PAI -enabling process characterization/ robustness studies. Experience with equipment design, technology transfer and facility fit. Strong technical writing and presentation skills, effectively communicating scientific thought and logic in oral and written presentations. Req ID9136 Position CategoryOperations Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/25/2014 7:33:40 AM

Senior QC Scientist

Frederick MD

Problem Solving & Communication Skills required: * Develops solutions to complex problems requiring ingenuity and creativity. * Applies knowledge of technical theories and principles on a broad base where analysis of situations or data requires an in-depth evaluation of various factors. * Frequent inter and intradepartmental collaborations. * Establishes contacts with outside centers of excellence in field of specialization and has contacts with customers and suppliers. * Has external alliances. * Active in professional organizations. Education & Experience Requirements: * BS Required, MS or PhD Preferred. * PhD 6-10 years relevant experience, MS 12+ years, or BS 14+ years. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9133 Position CategoryOperations Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/25/2014 7:33:40 AM

Senior Manufacturing Associate I/II, Manufacturing Compliance/Investigations

Gaithersburg MD

Position: * Write clear, concise, and organized summaries of investigations, product impact/process assessments, root cause analysis, and CAPAs. * Ensure all investigations are drafted to meet site specified timelines and support clinical demand of associated product(s). * Work closely with the all aspects of organization to remediate events and/or CAPA's necessary to close out the investigation. Coordinate involvement of cross functional teams with appropriate expertise. * Perform and understand investigation trending in order to determine appropriate CAPA's in response to trends. * Participate in meetings providing updates and follow-up to manage process & schedule. * Support internal and external inspections/audits. * Manage and increase the effectiveness and efficiency of Manufacturing Operation through improvements in a reduction of non-conformances, CAPAs, documentation errors and hold up of batch records. * Independently identify and resolve complex problems through good decision quality utilizing functional and technical skills. * Utilize OE principles and quality risk management. Education: Bachelors or Masters Degree (preferred): Engineering or Science Experience in multiple areas which may include Quality, Product Development or Manufacturing Operations. Knowledge of the processes and equipment involved in the manufacturing. Experience in validation activities associated with aseptic process, technology transfer and equipment and/or process validation. Experience in FMEA, QRM and Six Sigma preferred. Sr. MA I - 5+ years in the biotech /pharmaceutical industry. Sr. MA II - 7+ years in the biotech /pharmaceutical industry. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9130 Position CategoryDevelopment - Clinical Biologics Manufacturing Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/24/2014 7:25:31 AM

Facilities Maintenance Planner

Gaithersburg MD

Position: 5+ years in related BioTech, Pharmacuetical, or other regulated industry. 7-10 years in Engineering/Maintenance position preferred. 5+ Years experience with a CMMS (Computerized Maintenance Management System), Preferably SAP PM. Experience working with Microsoft Project - preferred Education: BS in Engineering/Technical field preferred or related practical experience CPMM (Certified Plant Maintenance Manager) and/or CMRP (Certified Maintenance and Reliability Professional) strongly preferred ~BSP *LI-MEDI Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesFrequent use and general knowledge of industry practices, techniques and standards. General application of concepts and principles. Develops solutions to a variety of problems of moderate scope and complexity. Refers to policies and practices for guidance. Works under only very general supervision. Work is reviewed for soundness of judgment and overall adequacy and accuracy. Contributes to the completion of organizational projects and goals. Errors in judgment or failure to achieve results would normally require a moderate expenditure of resources to rectify. Frequent internal company and external contacts. Represents organization on specific projects. Req ID9134 Position CategoryEngineering & Facilities Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/21/2014 7:26:26 AM

Packaging Specialist IV

Philadelphia (Non Sales) PA

**Multiple Openings** Position: *Execute packaging activities for all products as assigned *Work closely with Packaging Supervisor and Coordinator to ensure department priorities are met *Understand and follow GMP procedures required to package product to specification *Assign packaging operators to predetermined visual staffing plan *Understand the daily packaging schedule to maintain line operation *Monitor hour by hour packaging line performance and escalate as required *Ensure adherence to standard work package utilizing various line management initiatives *Communicate with team members to problem solve and resolve issues *Perform special assignments and other duties as required, as well as assist co-workers with problem solving *Ensure compliance with all regulatory requirements and Safety, Health and Environmental standards *Demonstrate extensive knowledge of processes and procedures in packaging operations *Complete required batch documentation and resolve issues *Participate in the design, development, or modification of area-specific processes or procedures *Complete assignments that require judgment, initiative, creativity and leadership in troubleshooting, suggesting alternatives, and making recommendations for continuous improvement *Demonstrate knowledge of supply chain management process as it relates to packaging operations *Execute various system based transactions as required *Execute training activities of operators for fulfillment of on the job training requirements *Demonstrate ability to work cross functionally with Quality Assurance, Quality Control, Facilities, Engineering, Materials Management and other business units *Work shifts and overtime as required Education: *High School diploma, General Education Degree (GED) or Associate Science Degree. Bachelor's degree is a strong plus. *6-8 years of related experience or training with no college degree. 4 - 6 years of related experience or training with a college degree. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional Notes*Ability to read and interpret documents such as safety procedures and manufacturing instructions *Ability to write routine reports, correspondence and status updates *Ability to speak effectively before groups of customers or other employees of the organization *Ability to calculate figures and amounts such as proportions and percentages *Ability to solve practical problems in situations where only limited information is available *Ability to work with Microsoft Office applications. SAP experience is preferred Req ID9080 Position CategoryManufacturing and Production Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/21/2014 7:26:26 AM

Setup Mechanic II

Philadelphia (Non Sales) PA

**Multiple Openings** Position: *Perform routine setup and maintenance for all product packaging equipment *Perform basic troubleshooting, adjustments, and repairs per GMP compliance standards *Work independently on off-shifts and call-ins in order to perform routine activities of the role on an emergency basis *Provide support to facilities and engineering teams with emergency, corrective and preventive maintenance work on all packaging equipment *Take a proactive approach to minimize potential equipment variances, deficiencies and breakdowns *Plan work activities to ensure packaging equipment is set up to run efficiently and within required timelines *Perform all job responsibilities in compliance with applicable regulations, standard operating procedures and industry practice *Adhere to all Medimmune Quality System policies and procedures as applicable for functional area *Work independently and without direct supervision to perform normal operating routines and emergency response procedures *Ensure all documentation and records (work orders, log books, etc) are accurate, complete and organized *Understand the daily packaging schedule, as well as monitor scrap levels and equipment performance. Address or escalate as required *Communicate with team members to problem solve and resolve issues Work closely with Packaging Supervisor to ensure department priorities are met *Perform special assignments and other duties as required, as well as assist co-workers with problem solving *Ensure compliance with all regulatory requirements and Medimmune Environmental, Health and Safety standards *Perform complex or specialized project assignments that may require working independently *Complete assignments that require judgment, initiative, creativity and leadership in basic troubleshooting, suggest alternatives, and make recommendations for continuous improvement *Communicate changes/events that may affect packaging schedule in a timely manner *Execute various system based transactions as required *Ensure fulfillment of on the job training requirements *Demonstrate ability to work cross functionally with Quality Assurance, Quality Control, Facilities, Engineering, Materials Management and other business units *Participate in all required and appropriate training *Demonstrate ability to work shifts and overtime as required *Flexibility to work shifts 3-6 years of related experience or training. Education: High School diploma, General Education Degree (GED) or Associate Science Degree. Bachelor's Degree is a strong plus ~BSP *LI-MEDI Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional Notes*Ability to read and interpret documents such as safety procedures and manufacturing instructions *Ability to write routine reports, correspondence and status updates *Ability to calculate figures and amounts such as proportions and percentages *Ability to solve practical problems in situations where only limited information is available *Ability to work with Microsoft Office applications. SAP experience is preferred. Req ID9089 Position CategoryManufacturing and Production Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/21/2014 7:26:26 AM

Director Medical Alignment - Oncology

Gaithersburg MD

Minimum Requirements: Advanced degree in science-related field, such as Pharmacology, Pharmacy, Medicine, or equivalent >3 years managing programs in a team environment Strong knowledge of medical strategy, clinical development, and medical science liaison areas Ability to manage a diverse group of responsibilities Ability to work effectively in a cross-functional team environment Preferred Requirements: Doctorate in Pharmacology, Pharmacy, Medicine, or equivalent MBA Oncology disease experience Minimum 5 years experience in a strategy-setting role within Medical Affairs Global experience within the pharmaceutical industry Working knowledge of FDA requirements Minimum Skills and Competencies: Leadership abilities Expert technical depth in disease area Strategic influencing skills Highly developed written and verbal communication skills Well-developed initiative ability Excellent project management skills Strong organization and time management skills Strong analytical and problem solving skills Preferred Skills and Competencies: Excellent computer skills (Excel, Word, Power Point, etc.) Knowledge of information/technology systems Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesSuccessful candidates will be AstraZeneca Employees and will be located at AstraZeneca's MedImmune strategic science center in Gaithersburg, Maryland. MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines. MedImmune is pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines BSP Req IDS142 Position CategoryMedical & Scientific Affairs Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/20/2014 7:25:47 AM

Manager I, CS&DM

Mountain View CA

Major Requirements: Minimum of 5 years in a related setting (clinical, data management or laboratory), with at least 2 years managing clinical trial data. Significant experience with relational databases, knowledge of the clinical trials process and GxP. Ability to query multi-table database for reporting, metrics and reconciliation purposes. 2 years prior management experience Experience with LabWare LIMS or other LIMS system preferred Computer Science background is a plus Advanced MS Excel skills required: including pivot tables, vlookup and logic functions Familiarity with SQL/Oracle queries Excellent interpersonal, oral and written communication skills Strong ability to communicate clearly and concisely Builds positive collaborative relationships with a variety of internal MedImmune staff and outside contacts. Understanding of overall clinical study process -- emphasis on understanding of clinical data flow and sample controls Excellent mentoring skills and ability to develop others Demonstrates strategic influencing, concern for standards, and thoughtful persuasion to obtain desired outcomes while maintaining effective, positive, organizational relationships Ability to independently prioritize workload with a sense of urgency in completing work assignments Proven ability to move projects to completion Proven, sustained record of high-quality independent work Proven ability to identify, manage and mitigate risk Ability to define problems, collect data, establish facts, and draw valid conclusions Education: Bachelor's Degree: Biotechnology; Life Sciences; or related fields Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9126 Position CategoryResearch - Translational Science Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/20/2014 7:25:47 AM

Manager/Senior Manager, R&D - Lab Automation

Gaithersburg MD

Education: For Senior Manager, BS with a minimum of 15 years of relevant experience or MS/PhD with 10-12 years of relevant experience. For Manager, BS with at least 10 years of relevant experience or MS/PhD with 5-8 years of relevant experience * The degree must be in Chemistry, Biochemistry, Biomedical engineering or a related field. Additional skills and knowledge needed for the job: * Experience with laboratory automation (TECAN, Hamilton, PerkinElmer, etc) is essential. * Working with external vendors for creating custom laboratory automation solutions. * Must have experience with establishing impactful collaborations internally and externally in developing high throughput methods. * Must have experience and skills in creating, modifying and troubleshooting laboratory robotics/automation scripts. * Experience in programming in C/C++, visual basic, .net is a must. * The successful candidate will play an important role on the development, optimization, and qualification of a wide variety of analytical assays as well as improving assay throughput/productivity through lab automation. * Successful candidate will present their research findings at internal and/or external meetings, and will serve as positive role model to other lab personnel. * Familiarity with various bio analytical methods is essential * Good verbal and written communication skills are must. Computer skills using Microsoft Word, PowerPoint and Excel are needed. * This individual must have a high level of initiative, independence and the ability to execute lab work under minimal supervision. * Experience with advanced VBA programming is a plus. Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional Notes Req ID9132 Position CategoryDevelopment - Analytical Biochemistry Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/20/2014 7:25:47 AM

Oncology Field Medical Science Liaison Lead

Gaithersburg MD

Minimum Requirements: * Doctorate in Pharmacology, Pharmacy, Medicine or equivalent experience. * Minimum of 3-5 years experience in pharmaceutical industry preferably in Medical Affairs or Clinical Development * Experience leading MSL teams * Experience with product medical strategy development and execution * Demonstrated expertise in drug information communication * Thorough knowledge of FDA requirements * Excellent interpersonal as well as oral and written communication skills * Strong knowledge of medical strategy, clinical development, and MSL areas * Knowledge of heath outcomes * Ability to manage a diverse group of responsibilities * Ability to work effectively in a cross-functional team environment Preferred Background: * MBA * 3-4 years of pharmaceutical Medical Science Liaison experience * >3 years experience in a strategy-setting role within Medical Affairs Skills and Competencies: * Builds and develops effective people and teams * Demonstrates personal commitment and enforces appropriate guidelines and policies * Manages performance and resources for functional area * Provides clarity and context around strategic direction as well as tactical execution * Applies organizational savvy * Builds relationships and employs appropriate interpersonal skills * Highly developed verbal and written communication skills * Well-developed initiative ability * Strong organization and time management skills * Strong analytical and problem solving skills * Life-long learner Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesSuccessful candidates will be AstraZeneca Employees and will be located at AstraZeneca's MedImmune strategic science center in Gaithersburg, Maryland. MedImmune is the worldwide biologics research and development arm of AstraZeneca, a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of small molecule and biologic prescription medicines. MedImmune is pioneering innovative research and exploring novel pathways across key therapeutic areas, including respiratory, inflammation and autoimmunity; cardiovascular and metabolic disease; oncology; neuroscience; and infection and vaccines BSP Req IDS143 Position CategoryMedical & Scientific Affairs Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/20/2014 7:25:47 AM

Sr. Manager, Clinical Contract Operations/Manager, Clinical Contract Operations

Gaithersburg MD

For the Sr. Manager level, we require more than 8 years of experience in pharma/biotech/CRO, including at least 7 years in clinical contracting. For the Manager level, we require a minimum of 8 years of experience in pharma/biotech/CRO, including at least 5 years in clinical contracting. Additionally, for both levels, we require the following education and experience: Bachelor equivalent degree in Science or Business is required. MBA or law degree is preferred. Experience in successfully executing clinical contracts from vendor selection through life-cycle management. Thorough understanding of the drug development process. People management experience preferred. Exceptional operational and negotiation skills. Ability to deliver with high quality at a fast pace. Excellent written and verbal communication skill. Good problem-solving and conflict resolution skills. Flexibility and ability to thrive in a rapid paced environment, manage effectively and capable of making difficult decisions in uncertain/evolving situations. *LI-MEDI ~BSP Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Req ID9124 Position CategoryClinical Operations Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/19/2014 7:19:44 AM

Supervisor - QA

Frederick MD

Position: 7- 10 yrs of QA experience. Prior night shift experience is desirable. Education: Bachelors in Sciences Equal Opportunity Employer Minorities/Women/Protected Veterans/Disabled/Sexual Orientation Additional NotesSolid operating skills including timely decisions, managing and measuring work along with good overall timeline and project management skills. Ability to develop staff and set mid and short term priorities. Builds and motivates teams. Ability to provide constructive feedback to staff. Ability to manage conflict and stand alone on certain issues. Adept at influence management of senior management, clients, and contractors/suppliers. Provides technical solutions to a wide range of difficult problems. Solutions are imaginative, thorough, practicable, and consistent with organizational objectives. Good understanding and wide application of technical principles, theories, and concepts in the field. General knowledge of other related disciplines. Frequent inter-organizational and outside customer contacts. Represents the organization in providing solutions to difficult technical issues associated with specific projects. Familiar with the use of OE tools/lean manufacturing, utilizing tools such as DMAIC and root cause analysis. Experience with Trackwise, SAP and Aegis is desirable. Knowledge of both US and international regulatory guidelines and standards. Req ID9120 Position CategoryOperations - Quality Refer A FriendApply Now MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune's approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune's approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency. MedImmune, LLC. is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. Information submitted will be used by MedImmune and its contracted partners for activities related to your prospective employment. MedImmune respects your privacy and any use of the information submitted will be subject to the terms of our Privacy Policy. MedImmune, LLC is an Equal Opportunity/Affirmative Action Employer

Posted On - 11/19/2014 7:19:44 AM

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