- Takeda Pharmaceuticals (Lexington, MA)
- …and PS + In collaboration with commercial functions, develop and implement strategies to control quality of drug substances and products based on the current ... (PS) with management and oversight of all project-related analytical control topics, development requirements and program milestones including global...Good/ Laboratory /Manufacturing Practice ( cGMP , cGLP) regulations + Harmonization… more
- Stony Brook University (Stony Brook, NY)
- …ongoing radiochemistry procedures for current clinical research studies, including production, quality control and metabolite analysis. The successful candidate ... radiochemistry facilities: the KAVITA AND LALIT BAHL Molecular Imaging Laboratory (https://cancer.stonybrookmedicine.edu/CancerResearch/BahlCenter) in the recently constructed Medical Arts and… more
- Catalent Pharma Solutions (Winchester, KY)
- …waist to chest height. Loading product of various amounts of completion to counters and quality control devices - Overhead lift and reach (≤15 lbs.). + Overhead ... committed to a Patient First culture through excellence in quality and compliance, and to the safety of every...equipment. All responsibilities are dictated by strict regulations (eg, cGMP , SOP, batch records). Shift: B/D Shift (6 PM-6… more
- Astrix Technology (Redwood City, CA)
- **QC Specialist - Biotechnology** Laboratory Redwood City, CA, US Pay Rate Low: 45 | Pay Rate High: 52 + Added - 03/10/2025 Apply for Job _Our client, a leading ... to drive analytical testing, ensure data integrity, and advance digital lab process improvements._ **Title: QC Specialist - Biotechnology** **Pay: $45-52/hr**… more
- BeOne Medicines (Pennington, NJ)
- …exercises. + Execute scale down model of manufacturing processes. Maintains a good laboratory practice. + Author and maintain process control strategy documents ... for DP raw materials and in-process samples. + Author and maintain process control strategy documents throughout the lifecycle of a program and maintain process risk… more
- Grifols Shared Services North America, Inc (Dallas, TX)
- … Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice ( cGMP ) and internal company procedures. + Supervise donor selection, plasma ... FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP . + Attend all required training sessions, staff meetings,...Manager and/or the Assistant Manager. + Assist in the control of center donor funds as determined by the… more
- Biomat USA, Inc. (Lorain, OH)
- … Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice ( cGMP ) and internal company procedures. * Supervise donor selection, plasma ... FDA approved Standard Operating Procedure Manual, OSHA, CLIA and cGMP . * Attend all required training sessions, staff meetings,...Manager and/or the Assistant Manager. * Assist in the control of center donor funds as determined by the… more
- Endo International (Rochester, MI)
- …work to bring the best treatments forward. Our shared values of Integrity & Quality , Innovation, Drive, Collaboration and Empathy guide our team and enable us to ... maintains cooperative cross-functional relationships with peers and leadership in Quality , Operations, Pharmaceutical Technology, and Supply Chain to meet… more
- Fujifilm (Holly Springs, NC)
- …This role works with multiple functions to support operations (eg, Warehouse, Supply Chain, Quality Control (QC)). The Raw Material Sampler 2 uses Systems and ... (SAP) Enterprise Resource Planning (ERP) system for inventory management and Laboratory Information Management System (LIMS) for sample management while operating in… more
- PCI Pharma Services (Madison, WI)
- …highly desirable. + Experience performing RCA, technical writing, and working with quality related investigations. + Knowledge of laboratory and production ... PCI. The Senior QA Manager will work with other departments to ensure the quality of products and compliance to internal procedures and external standards. The role… more
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