- Lilly (Concord, NC)
- …up. The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC ( GMP and non GMP ) and the ancillary systems associated within the facilities. During ... responsible for effectively, reliably, and cost effectively operating the site's HVAC ( GMP and non- GMP ) and ancillary systems associated within the facilities,… more
- Merck (Durham, NC)
- **Job Description** The Quality Associate Director/ GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the ... (5) years of manufacturing, technology, laboratory, and/or quality operations experience within GMP environment + GMP Compliance knowledge and proficiency in… more
- Kelly Services (Petersburg, VA)
- …the process safety activities associated with technology transfer, process design, and GMP startup (4) Lead process safety assessments, Management of Change (MOC), ... and the implementation and verification of safeguards in GMP manufacturing (5) Lead PFMEAs, PHAs, and PSSRs for new and existing API processes; translate outcomes… more
- Astrix Technology (Torrance, 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
- Merck (Rahway, NJ)
- …portfolio needs, and ensure predictable, on-time delivery of clinical batches with impeccable GMP compliance for the filling line asset in scope of the expansion ... operational requirements with C&Q activities; ensure equipment and facilities are released for GMP use and ready for clinical campaigns. + Establish and maintain … 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 (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
- 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
- ABM Industries (Oceanside, 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
- 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