- Sanofi Group (Swiftwater, PA)
- **Job title: Device Regulatory Lead ( Associate Director)** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... thought was possible. Ready to get started? **Main responsibilities** + Serve as Device Regulatory Lead on assigned project teams (early phase, late stage… more
- Teva Pharmaceuticals (West Chester, PA)
- …registration. This position comes with 4 direct reports (Dir, Sr Manager, Manager & Associate III). The Sr Director, Regulatory Affairs CMC is responsible for ... Senior Director Regulatory Affairs CMC (Biologic Products) Date: Jun 13,...associated with product development including product and process development, device development, analytical methods, formulation development, manufacturing, and labeling.… more
- Zimmer Biomet (PA)
- …respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to enable the ... key functional areas - Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio as owned by… more
- CSL Behring (King Of Prussia, PA)
- **The Opportunity** As the Regional Lead for the Enterprise Contracting Center of Americas (US, Canada, LATAM), you'll help foster meaningful relationships and ... creative contracting, this is the role for you. This is an Associate Director level role. **The Role** **Key Responsibilities:** 1. **Stakeholder Support:** +… more
- Merck (West Point, PA)
- …operational/ regulatory requirements for all dosage forms (liquid, lyo, drug- device combinations) + Review and approval of data and technical documents + ... of vaccine drug products and various innovative technology platforms. The candidate will lead and direct the development for a range of vaccine modalities within our… more
- Dentsply Sirona (York, PA)
- …FDA, ISO, EPA and OSHA guidelines and regulations. Ensures full compliance with regulatory , safety and Human Resources programs within manufacturing. + Lead ... Action (CAPA). + In conjunction with both the Quality and Regulatory Affairs Departments, drive quality investigations for consumer complaint issues, issue… more
- Omnicell, Inc. (Warrendale, PA)
- …skills **Preferred Qualifications** + ISO 9001, ISO 13485 or FDA Regulated Medical Device experience + Associate degree and minimum three (3) years of ... procedures + Maintain identification and traceability of parts per regulatory requirements + Maintain documentation for supplier certifications +...all. + In **Doing the Right Thing** , we lead by example in ALL we do. We value… more