- Danaher Corporation (Muskegon, MI)
- …Muskegon site Validation Master Plan. This position reports to the Quality Assurance Manager and is part of the Quality Assurance Department located in Muskegon, MI ... if you also possess previous experience in: + Life Science, Pharmaceutical , Medical Device or Biopharma manufacturing environments. + Analytical and problem-solving… more
- Abbott (Alameda, CA)
- …for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed. + Participate in cross-functional clinical team(s) in the planning ... in conducting medical device and/or _in-vitro_ diagnostics studies preferred. Pharmaceutical background may also be considered. **Skills** + Demonstrated excellence… more
- East Boston Neighborhood Health Center (East Boston, MA)
- …and communities. Whether you're a nurse or physician providing direct care, a manager leading dedicated teams, or part of the essential support staff who keep ... various non-skilled nursing tasks, for the maintenance and control of non- pharmaceutical supplies and equipment, and for assigned support activities. This position… more
- AbbVie (Worcester, MA)
- …. Job Description The Associate Director, Third Party Manufacturing (TPM) Manager will be the main supplier relationship contact person in charge ... development and planning skills coupled with necessary knowledge of pharmaceutical development, manufacturing and supply activities. + Issue identification and… more
- Sanofi Group (Swiftwater, PA)
- …site. This position reports to and supports the area team Metrology Manager who is ultimately responsible for the efficient, effective, and reliable operation ... associated control and recording systems. + Previous experience in cGMP or pharmaceutical manufacturing environments. **Why Choose Us?** + Bring the miracles of… more
- DEKA Research & Development (Manchester, NH)
- …Device Research and Development environment. The position reports to the Product Complaints Manager . This is a high visibility role with a significant direct impact ... or product analysis. + Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and… more
- DEKA Research & Development (Manchester, NH)
- …Device Research and Development environment. The position reports to the Product Complaints Manager . This is a high visibility role with a significant direct impact ... or product analysis. + Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and… more
- AbbVie (Worcester, MA)
- …Description The Associate Director, Project Engineering will serve as a true project manager who is responsible for leading large global projects that contributes to ... A technical background in health care, medical devices, biological, or pharmaceutical companies. + Consistently demonstrated competency with financial systems and in… more
- PruittHealth (Valdosta, GA)
- …medication in appropriate container for correct dispensing system. * Mixes pharmaceutical preparations according to written orders. * Labels medication container ... department. * Pulls stickers for reorder items and forwards them to Inventory Manager . * Places received stock on shelves accurately. * Keeps medication storage area… more
- DEKA Research & Development (Manchester, NH)
- …Device Research and Development environment. The position reports to the Product Complaints Manager . This is a role with direct impact to the Quality Management ... setting is preferred. + Knowledge of FDA requirements for Quality Systems, pharmaceutical products, and Medical Device Reporting regulations (21 CFR 803, 820 and… more