- Lilly (Durham, NC)
- …Process Technician is responsible for providing support and QA oversight to GMP operations in the Warehouse and Logisitics area. The Technician supports multiple ... regular presence in warehouse and logistics areas to monitor GMP programs and quality systems. + Reviews and approves... programs and quality systems. + Reviews and approves GMP documentation in support of daily operations such as:… more
- Merck (Durham, NC)
- …**Required Experience and Skills:** + At least one (1) year GMP manufacturing/processing experience. + Demonstrated written and verbal communications skills. + ... Literacy, Digital Literacy, Driving Continuous Improvement, Freeze Drying, Global Manufacturing, GMP Compliance, GMP Operations, Good Manufacturing Practices (… more
- Bristol Myers Squibb (Indianapolis, IN)
- …a team responsible for producing RayzeBio's radioisotopes under Good Manufacturing Practices ( GMP ). Additionally, you will be the front line in ensuring compliance ... line clearance, cleaning, equipment setup, etc.) while ensuring compliance with GMP , NRC regulations, and management expectations. + Prepare reagents and assembly… more
- Cambrex High Point (High Point, NC)
- …today! Job Overview Process Technician 1 will conduct activities associated with the GMP Kilo and Pilot Plant at Cambrex. These activities include material handling, ... suites. + Basic knowledge of equipment and facility maintenance for the GMP and large-scale production areas. Basic ability to clean equipment and manufacturing… more
- Amgen (Thousand Oaks, CA)
- …process improvements, support new technology introductions, and maintain robust GMP manufacturing performance. Your work will directly contribute to Amgen's ... owner, reviewer, or data verifier, ensuring accuracy and compliance with current GMP and Amgen standards. + Maintain documentation to accurately reflect operational… more
- Catalent Pharma Solutions (Harmans, MD)
- …on-site Catalent, in Baltimore & Harmans, Maryland, provides industry-leading GMP development and manufacturing services for cutting-edge biopharmaceuticals such as ... I-III and commercial programs. The Director, QC Analytical assures compliance to GMP and company specifications as well as relevant pharmacopeia compendia. The… more
- Bristol Myers Squibb (Indianapolis, IN)
- …in ensuring compliance in operations to support clinical development and GMP commercial operations in accordance with RayzeBio policies, standards, procedures and ... of investigations, CAPAs, change controls, validation documentation, and other related GMP documentation. + Identify and report discrepancies from required work… more
- Gilead Sciences, Inc. (Foster City, CA)
- …digital ambitions. The scope of this role will include the existing API and OSD GMP manufacturing facilities as well as take a leading role in designing a new state ... AI-driven data flows. + Standardize architecture for LIMS, MES, PCS, Historian, e-Validation, GMP and non- GMP reporting, and AI-enabled digital systems. + Ensure… more
- Dairy Farmers of America (Fort Morgan, CO)
- …and clean packaging equipment. Perform minor equipment maintenance. Adhere to all GMP , HACCP, safety, regulatory, and plant policies and procedures. Promote safety, ... Attend required training, including but not limited to, Safety, GMP , Hazard Analysis and Critical Control Point (HACCP), and...they arrive + Follow all DFA good manufacturing practices ( GMP ) and work in a manner consistent with all… more
- Lilly (Indianapolis, IN)
- …the world. **Position Brand Description:** Early Phase Quality Assurance is accountable for GMP Quality dedicated to the PR&D Early Phase Team. This position is ... to be used in Clinical Trials including management and review of GMP documentation, analytical results and regulatory commitments. + Coordinate deviation and… more