- ThermoFisher Scientific (Plainville, MA)
- …and drug product technology transfer activities. + Lead technology transfer to GMP from clients or the internal development team, including process/facility gap ... assessments and drafting/reviewing GMP documents (batch records, tech transfer protocols, sampling plans). + Lead the downstream tech transfer team; build and… more
- Herbalife (Winston Salem, NC)
- …+ Assist production staff with the correct understanding and implementation of GMP procedures and company policy + Document and investigate (as appropriate) foreign ... rejected, hold, etc. + Document quality-related incidents using appropriate GMP documentation (eg, nonconforming materials report, unplanned deviation report,… more
- BeOne Medicines (Pennington, NJ)
- …with a primary focus on capillary electrophoresis techniques to support GMP manufacturing, testing, and release of material, intermediates and finished biological ... Review, interpret, and report analytical data in accordance with GMP regulations and internal procedures. + Lead troubleshooting efforts...for the laboratory. + Participate in internal and external GMP audits, as needed. + Train other junior level… more
- Kelly Services (Malvern, PA)
- …new production introduction (NPI) tech transfers into the manufacturing area to enable GMP production of DS clinical supplies + Setup and lead project kickoff ... Chain (CSC) teams and the Site Operations team, regarding tech transfer and GMP DS clinical supplies updates + In collaboration with Site Operations and Quality,… more
- ABM Industries (San Diego County, CA)
- **Overview** **Job Summary Details:** The GMP (Good Manufacturing Practices) Cleaner plays a critical role in maintaining cleanliness and hygiene standards within ... **Preferred Qualifications:** * Previous experience in cleaning within a GMP -regulated environment, preferably in the pharmaceutical or healthcare industry. *… more
- Boehringer Ingelheim (Athens, GA)
- …**Duties & Responsibilities** + Responsible for managing higher level, more complex GMP validation project activities at the BIAH US locations from concept through ... scientific, bioengineering or relevant discipline + Six (6) years GMP validation or similar experience in a GMP... GMP validation or similar experience in a GMP manufacturing or similar production environment + Minimum of… more
- Astrix Technology (Holly Springs, NC)
- …are seeking a Manufacturing Associate to join our dynamic team and support GMP drug substance manufacturing and validation activities. This individual will play a ... operations and support activities on the production floor. + Perform GMP and non- GMP production runs (small- and large-scale). + Handle material preparation,… more
- Astrix Technology (New Brunswick, NJ)
- …in maintaining and supporting facility and equipment operations within a GMP biotechnology manufacturing environment. This position is responsible for both facility ... preventive maintenance, troubleshooting, and repair activities, while maintaining full GMP compliance and documentation standards. **Location:** Middlesex County, NJ… more
- Amgen (Holly Springs, NC)
- …will act as the Manager for the New Product Introduction (NPI) Team in GMP Drug Substance Supply. This position is within Amgen North Carolina (ANC) Manufacturing ... and GMP Supply - Manufacturing Support organization. ANC is a...an important supply facility for Amgen's pipeline products. The GMP DSS plant manufactures drug substance for clinical trials… more
- Astrix Technology (Los Angeles, CA)
- …and other techniques, and in-process test method + Follow approved GMP manufacture directions such as Master Batch Records, Standard Operation Procedures, ... Standard Test Procedures and other procedures to manufacture GMP materials, perform in-process test, package the product including other related activities + Perform… more