- Nestle (Bohemia, NY)
- …highest standards of SOPs and current Good Manufacturing Practices (cGMPs). You'll lead daily quality activities on the production floor while actively contributing ... and assists in developing solutions. + Responsible for plant GMP audits and the Glass and Hard Plastic program;...work experience. + Knowledge of FDA regulations for the GMP of Dietary Supplements and Foods. + Experience with… more
- ThermoFisher Scientific (Miami, FL)
- …lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, ... maintenance machining/welding shop. + Communicate daily with the Maintenance Team Lead about significant information. + Assists in analyzing and correcting problems… more
- Amgen (Holly Springs, NC)
- …world. In this vital role you will communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance ... some upstream process unit operations. + New Product Introduction (NPI) lead coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities… more
- ThermoFisher Scientific (St. Louis, MO)
- …Standard (Mon-Fri) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office **Job Description** When you're part of ... to impacted areas and leadership. + Coordinate and effectively lead cross-functional teams through complex investigations, and complete milestones on-schedule.… more
- Kelly Services (Petaluma, CA)
- …Standard Operating Procedures (SOPs) and QC protocols for microbiological analyses. + Lead the method development and validations for all analyses, such as LAL ... findings. + Participate in internal/external audits and ensure regulatory adherence ( GMP , FDA). **Qualifications:** + Bachelor's or Master's degree in Microbiology,… more
- Actalent (Irvine, CA)
- …ManagerJob Description We are seeking a Quality Assurance Manager to lead the development, maintenance, and improvement of technical documentation, including SOPs, ... will ensure all documentation is accurate, complete, and compliant with GMP , FDA, NSF, and other relevant regulatory requirements. Responsibilities + Oversee… more
- Actalent (San Clemente, CA)
- …in accordance with ICH and other relevant standards. Responsibilities + Lead quality engineering activities for the development and manufacturing of drug-eluting ... stents. + Oversee drug coating processes, ensuring compliance with GMP , GLP, and ICH guidelines. + Manage equipment validation protocols (IQ, OQ, PQ) and support… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …contract laboratories for methods development/method transfer/QC testing. + Assume a lead SME role in analytical chemistry related team roles and responsibilities ... of method development, method validation and transfer principles in a GMP setting. + Hands-on experience and expertise with Mass Spectroscopic detectors… more
- ManpowerGroup (Milpitas, CA)
- …within 30 minutes during on-call periods **What's the Job?** + Lead all facilities operations, maintenance, and regulatory compliance within a pharmaceutical ... activities, change control procedures, and regulatory inspections to maintain GMP standards. **What's Needed?** + Bachelor's degree in Mechanical Engineering,… more
- BD (Becton, Dickinson and Company) (Los Angeles, CA)
- …in accordance with current ISO (International Organization for Standardization) and GMP (Good Manufacturing Practices) standards. + Provide clear, timely, and ... or as requested by other business functions in accordance with current GMP requirements. + Report and document all customer complaints in appropriate systems… more
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