- Actalent (Boston, MA)
- Job Title: QMS Specialist (25/hrs. per week) We are seeking a highly skilled QMS Specialist with experience in a GMP-regulated environment, ideally ... regulations for GMP compliance is essential. Responsibilities + Assess current QMS processes, identify areas for improvement, and implement effective solutions to… more
- DEKA Research & Development (Manchester, NH)
- DEKA R&D has an immediate opening for a Quality Systems Specialist to work in the Quality Department in a dynamic Medical Device Research and Development ... and Approve Quality System Records + Process changes for QMS Procedures (SOPs) + + Make red-line changes +...and distribute via electronic system + Track training for QMS documents within the Change Order process + Track… more
- Carrier (Beverly, MA)
- …. **About This Role:** The Cybersecurity & Application Specialist operates independently, conducting multidisciplinary research and performing System ... to identify, prioritize, and address security-related issues. Additionally, the specialist provides assurance, both internally and externally, to demonstrate the… more
- Hologic (Marlborough, MA)
- Medical Device Reporting Specialist Marlborough, MA, United States We are seeking a detail-oriented and proactive Medical Device Reporting Specialist to join our ... ensuring compliance with applicable regulations and quality management systems ( QMS ) requirements, specifically related to the assessment, documentation, and… more
- Corning Incorporated (Tewksbury, MA)
- Regulatory Affairs Specialist , Biologics **Date:** May 3, 2025 **Location:** Tewksbury, MA, US, 01876 **Company:** Corning Requisition Number: 67375 **The company ... productivity and enable breakthrough discoveries. **Role Summary** Regulatory Affairs Specialist (biologics focused) provides necessary support to regulatory affairs… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- We are seeking a highly skilled, self-motivated **Senior Validation Specialist - CSV** to ensure compliance of computerized systems with regulatory requirements in ... GAMP 5, and Annex 11. **As a Senior Validation Specialist , a typical day might include:** + Planning and...facility; GMP experience is required. Experience with ERP, LIMS, QMS and other GxP-regulated computerized systems and analytical instruments… more