- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Investigations Supervisor as part of the Technical Operations team based in Raritan, New Jersey. ... Role Overview The CAR -T Investigation Supervisor will work with the investigation team to help...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Catalent (Philadelphia, PA)
- QA Supervisor Position Summary Catalent Pharma Solutions in Philadelphia, PA is hiring a QA Supervisor . The QA Supervisor will p rovide Quality Assurance ... categoriesCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- The QC Microbiology Supervisor leads, and monitoring the daily operations, activities, and workflow for the laboratory personnel. Additionally, you will implement ... testing standards, policies and ensure safety measures are followed. The supervisor will assist laboratory personnel with career development, performance and other… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Operations Supervisor (2nd shift) as part of the Technical Operations team based in Raritan, ... NJ. Role Overview The Operations Supervisor is an exempt level position working within Technical...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Facility Supervisor as part of the Maintenance & Metrology team based in Raritan, NJ. ... Role Overview The CAR-T Facility Supervisor is an exempt level position working within Technical...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QA Investigations Supervisor (2nd shift) as part of the Quality team based in Raritan, NJ. ... Role Overview The QA Investigations Supervisor has the responsibilities for providing quality oversight over...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking QC Investigations Supervisor as part of the Quality Control team based in Raritan, NJ. Role ... Overview The QC Investigations Supervisor is an exempt level position with responsibilities for...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Supervisor , QC Micro as part of the Quality Control team based in Raritan, NJ. ... Role Overview The QC Microbiology Supervisor , CAR-T Manufacturing is an exempt level position with...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a Warehouse Supervisor as part of the Technical Operations team based in Raritan. Role Overview ... The Warehouse Supervisor will be part of the Technical Operations team...uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free… more
- Catalent (Manassas, VA)
- …services to solve difficult development and manufacturing challenges.The Quality Assurance Supervisor will lead Food Safety and Quality programs. This includes ... categoriesCatalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking a Training Supervisor - Operations as part of the Training team based in Raritan, NJ. ... citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. Legend Biotech maintains a drug -free workplace. more
- Catalent (San Diego, CA)
- …methods for peptide and small molecule API, intermediates, and drug products from scratch.Develop cleaning verification methodsPerform and train others ... friability testing.Troubleshoot and optimize analytical methods for characterization of drug products and intermediatesPerform qualification studies to determine if… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and immune disorders. Summary Position leads very complex studies or entire drug project in study design, data analysis and interpretation of results independently ... with minimal supervision. This position provides input to entire drug development plans with minimal supervision and authors regulatory responses and other documents… more
- Merck & Co. (Durham, NC)
- …role will contribute to the performance and results of a E2E drug substance/product department and provide technical guidance. Off-shift and weekend coverage will ... is in direct support of our Upstream Fermentation manufacturing process for Bulk Drug Substance. Focused areas of responsibility include but are not limited to… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on ... deviation reports and elevate issues to the attention of the supervisor .Compile and maintain a monitoring review spreadsheet.Compile and maintain CRO Oversight… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on ... deviation reports and elevate issues to the attention of the supervisor .Compile and maintain a monitoring review spreadsheet.Compile and maintain CRO Oversight… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …sanitation, and documentation activities associated with the production of drug products. This position supports the ongoing development, manufacture, and ... corporate policies, and the regulatory requirements of the US Food and Drug Administration. Job Responsibilities: Perform duties associated with the compounding of… more
- Catalent (St. Petersburg, FL)
- …activities and schedule for the QA Specialists.Provides feedback to QA Supervisor and Manager on performance of QA Specialists.Responsible for actively identifying ... DRB (Deviation Review Board) presentation.Effective communication with Quality Assurance Supervisor and Manager regarding status of daily work.Serve as administrator… more
- Catalent (Philadelphia, PA)
- …PA is hiring a QA Inspector. This position reports to the Quality Supervisor . The Quality Inspector is responsible for process monitoring and auditing of packaging ... for packaging job(s) and/or operation(s) to ensure that the drug product quantities documented in the batch record match...rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring… more
- BioAgilytix (Durham, NC)
- …fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll gain experience with a variety ... I or II, leading the development and validation of Anti- drug Antibodies (ADA) and Pharmacokinetics (PK) assays, playing a...of MS Excel and WordDemonstrated experience serving in a supervisor role and leading teams Knowledge and application of… more
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