- Bristol-Myers Squibb Company (Summit, NJ)
- …the standards to site MS &T at internal and external sites. The validation lead is accountable for developing equipment, facility, and process validation ... of priorities, develop a strategic vision. The Cell Therapy Validation Lead will cover process, equipment, and...validation when in pivotal trials. Qualifications & Experience BS/ MS .S/Ph. D in Chemical Engineering or Life Science… more
- BioAgilytix (San Diego, CA)
- …experience, strong understanding of LC- MS / MS method development and validation , and demonstrated ability to lead large, regulated teams in delivering ... ensure timely completion of studies.Serve as Principal Investigator or Study Director for GLP/ validation projects, reviewing data, methods, and… more
- Eisai, Inc (Exton, PA)
- … Director writes, reviews, and/or approves GMP documents, including validation protocols and reports, and SOPs, along with providing supporting documentation. ... If this is your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is responsible for leading and building a… more
- Merck & Co. (San Francisco, CA)
- …data-driven decision-making. Under the broad guidance of the DSCS Digital Program Mgmt Lead , the Associate Director , DSCS Digital Project Manager, will be ... Job Description Position Description: Associate Director , DSCS Digital Implementation Project ManagerWithin the Development...with a strong background in the biotech industry to lead digital transformation initiatives. This role will focus on… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Director of Operations as part of the Technical Operations team based in Raritan, ... NJ. Role OverviewThe Director of Operations is an exempt level position working...ensure safe and compliant manufacturing operations according to cGMP requirements. Lead a ~250+ organization responsible for either the non-sterile… more
- Eurofins (St. Charles, MO)
- …also support BioTherapeutics Services based on business needs Develops Liquid Chromatography- Mass Spectrometry (LC- MS ) methods for ADME/ DMPK applications ... Basic Minimum Qualifications (BMQ): Direct/ Demonstrated experience with Liquid Chromatography- Mass Spectrometry (LC- MS ) in a contract research… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …oversees resource planning for GDX global and regional projects requiring Validation services and Technical Lead assignments.ResponsibilitiesOversee and manage a ... medical needs of people globally by leveraging our world-class science and technology. With more than 125 years of...4+ years of proven leadership experience managing technical and validation teams, preferably at Director or Senior… more
- IntePros (Audubon, PA)
- IntePros is currently looking for a Director of Quality to join one of our growing Medical Device clients in Audubon, PA. The Director of Quality will Provide ... system performance while ensuring compliance with all company policies and procedures. Lead and enforce regulatory compliance with US FDA, State, OSHA and… more
- ACIST Medical Systems (Eden Prairie, MN)
- Job Description Position Summary: The Senior Director , Product Quality leads and manages global product quality activities for the ACIST/BMT product lines across the ... to enhance patient safety and product performance; leading verification and validation (V&V) activities and monitoring post-market product quality to drive… more
- Sangamo Biosciences, Inc. (Richmond, CA)
- JOB SUMMARY: The Director , Vector Production will oversee activities related to the Process Development and in-house non-GMP/cGMP production of recombinant ... house for use in R&D and pending facility decisions Lead in-house team producing rAAV Co-ordinate production activities with...the ongoing security of the supply chain for raw materials and intermediates to ensure the uninterrupted performance of… more
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