- Bristol Myers Squibb (Princeton, NJ)
- …5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading ... assessing regulatory risk, and developing global filing strategies. + Co- lead marketing application submission teams for indications that are at regulatory… more
- Novo Nordisk (Princeton, NJ)
- …regulatory agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/ Lead Regulatory Scientist/Sr. Manager ... related experience; including hands on related pharmaceutical or medical device /pharmaceutical combination product experience and actual regulatory experience… more
- Kelly Services (Horsham, PA)
- …time. This Regulatory Affairs Coordinator will help administer the day-to-day Regulatory Affairs operations as directed by the Associate Director related to ... Kelly Science and Clinical FSP is currently seeking a Regulatory Affairs Specialist for a long-term engagement with one...of the business. In this role, you will: + Lead and manage activities concerned with the submission and… more
- Integra LifeSciences (Plainsboro, NJ)
- …challenging what's possible and making headway to help improve outcomes. The Warehouse Lead operator will verify and keep records of all incoming and outgoing ... inventory locations, and perform all associated transactions in ORACLE. The Warehouse Lead will perform all required duties in compliance with company policies, US… more
- Bristol Myers Squibb (Princeton, NJ)
- …medical device , and/or translational development processes, with ability to lead supportive project management processes + Strong understanding of global ... the patients and health care providers we serve. The Associate Director, Technical Management, reports to the Technical Management...regulatory requirements for companion diagnostic device development… more
- AbbVie (Branchburg, NJ)
- …Team (IEST) lead , Clinical Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director, Clinical Development should expect to ... on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global or regional responsibilities and… more
- Integra LifeSciences (Plainsboro, NJ)
- …help improve outcomes. The ** Lead Quality Inspector** serves as a Lead Associate , Quality Inspector for the Plainsboro Manufacturing Site, Collagen ... Manufacturing Center (CMC). The lead associate is responsible for performing and/or...policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory … more
- J&J Family of Companies (Titusville, NJ)
- Associate Director, Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part of ... the Johnson & Johnson Family of Companies, is recruiting for an Associate Director, Temperature Strategy & Execution within Clinical Supply Chain (CSC). The position… 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
- Envista Holdings Corporation (Quakertown, PA)
- …as primary lead for hourly employee completion of annual survey + Lead site community involvement and associate recognition initiatives and programs such as ... growing, energetic, and diverse mix of professionals spanning engineering, operations, regulatory and quality backgrounds that work collaboratively in the fast-paced… more