- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the ... critical role ensuring product safety and compliance in the medical device industry. **Responsibilities** + **Lead Post-Market Surveillance Activities:** Oversee the… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …Affairs, you will be responsible for leading RA team members involved in device project activities and new product development in Advanced Drug Development Delivery ... of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products...of regulatory affairs experience within the pharmaceutical or medical device industries, ideally with expertise in drug- device … more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the ... bodies, review design control documents and product labeling, and evaluate proposed device changes. The Sr. Regulatory Affairs Specialist is able to interpret and… more
- Integra LifeSciences (Plainsboro, NJ)
- …is responsible for the medical dispersion production activities for CMC (Collagen Manufacturing Center) to ensure the safety, efficacy, and quality of our medical ... conducted in compliance with ISO 7 Clean Rooms and with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and… more
- J&J Family of Companies (Raritan, NJ)
- …technical support to multidisciplinary project teams in the design, development, and manufacturing of various devices primarily within wound closure and healing. + ... supply chain functions to ensure proper implementation and process controls for manufacturing processes. + Provide technical support for marketed medical device … more
- Integra LifeSciences (Plainsboro, NJ)
- …overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be ... appropriate test records. + Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. +… more
- Integra LifeSciences (Plainsboro, NJ)
- …overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be ... appropriate test records. + Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. +… more
- Kelly Services (Raritan, NJ)
- …Chemist** Kelly OCG a Polymer Chemist for our client a leading medical device company in Raritan, NJ. If you're passionate about bringing the latest scientific ... with Polymer Process Engineers to optimize process parameters for large-scale manufacturing . The ideal candidate will possess a solid background in polymer… more
- Integra LifeSciences (Plainsboro, NJ)
- …overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be ... appropriate test records. * Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. *… more
- Integra LifeSciences (Plainsboro, NJ)
- …overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be ... appropriate test records. + Perform line clearances and quality reviews in manufacturing , labeling, or other assigned areas during manufacturing activities. +… more