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Manager - Supplier Quality Maryland
9/27/2016 6:10 AM

The QA Manager provides leadership and guidance to a number of functional areas including manufacturing, facilities, and other quality departments, and may support manufacturing operations at contract facilities. Interprets and implements quality policies, manages quality systems, and assists in facilitating regulatory compliance inspections.

The QA Manager supervises Quality Assurance Sup
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Scientist I/Scientist II, Antibody Drug Conjugate/Bio-conjugation Maryland
9/27/2016 6:10 AM

This position can be filled at either a Scientist I/Scientist II level depending upon experience.

The position is for an innovative and highly-motivated scientist who will join the Antibody Drug Conjugation (ADC) team at MedImmune's headquarter in Gaithersburg (MD). The candidate will be responsible for optimization and development of bioconjugation processes, for developing novel antibody
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Project Manager Maryland
9/27/2016 6:10 AM

The project manager will be part of the Access Services Project Management Office (PMO). The project manager is responsible for the effective management of cross functional project teams and the efficient governance of the project. This includes planning, executing, milestone tracking, monitoring variances to plan and budget, reporting progress to stakeholders and ultimately ensuring all project m  ...View Job
Associate Scientist II/Scientist I Maryland
9/26/2016 6:34 AM

As part of the Upstream (Cell Culture) Manufacturing Sciences and Technology (MS&T) organization, the successful candidate will be responsible for supporting technology transfer of therapeutic protein (primarily monoclonal antibodies) processes from our development organization into one of the two mammalian production facilities located at the Frederick Manufacturing Center. The incumbent will  ...View Job
Associate Scientist I/Associate Scientist II, In Vivo Pharmacology - CVMD Maryland
9/26/2016 6:34 AM

This position can be filled at either the Associate Scientist I or Associate Scientist II level depending upon experience.

The successful candidate will be expected to help design, execute and analyze in vivo pharmacology studies in mouse and rat models of obesity, diabetes and NASH. He/she will contribute to various in vivo research activities within the CVMD Research group including mode
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QA Specialist III - Compliance Maryland
9/26/2016 6:34 AM

Responsibilities include but are not limited to:  Perform daily operations to support deploy Supplier Quality Systems as related to creation, review and approval of vendors files, reviews of approved vendor lists for cGMP direct and indirect materials  Maintains Supplier Quality in a state of compliance with current good manufacturing practice regulations  Fo  ...View Job
Scientist I, Medical Device Engineer Maryland
9/26/2016 6:34 AM

The candidate will be a part of MedImmune drug delivery and device development group responsible for combination product development involving parenteral injection devices delivering biologics and peptides. This position is in the device development platform group and will play a critical role in the design and testing of state-of-the-art platform injection devices.

This role will support
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Scientist II / Senior Scientist, Analytical Biochemistry, Late Stage Biologics Maryland
9/26/2016 6:34 AM

This position can be filled at Scientist II or Senior Scientist level depending upon experience.

Late stage biologics group in Analytical Sciences Division within Biopharmaceutical Development Department has an opening for a Scientist II/ Senior Scientist for supporting a wide range of biologicals in late-stage development for regulatory filings and subsequent lifecycle management activiti
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Manager, Capacity Planning Colorado
9/26/2016 6:34 AM

* Responsible for partnering with operations and MS&T to determine constraints through debottlenecking analysis. * Oversees development of product bills of capacity and maintenance of assumptions for capacity planning at each defined level, including Rough Cut Capacity Planning (RCCP) and Capacity Requirements Planning (CRP). * Partners with operations to ensure development and ongoi  ...View Job
QA Specialist III Maryland
9/26/2016 6:34 AM

Responsible for assuring the quality of licensed or clinical products manufactured at MedImmune or at contract manufacturing sites. The QA Specialist supports and provides advice to a number of functional areas including Manufacturing, Facilities & Engineering, Quality Control, and other departments. Interprets and implements quality procedures, manages quality systems and assists in maintaini  ...View Job
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