- Merck (Rahway, NJ)
- …Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform Packaging and ... to ensure compliance with relevant regulations and standards. Ensure thorough engineering, medical device and packaging science is applied to deliverables for… more
- Medtronic (Newark, NJ)
- …understanding of regulatory requirements and industry standards governing medical device reprocessing. + Excellent communication, interpersonal, and ... instrumentation. Commitment to upholding the highest standards of safety and quality in medical device reprocessing. + This position is in the east coast of US… more
- Merck (Rahway, NJ)
- …advanced degree (Master's or PhD) preferred. + Minimum of 10 years of experience in medical device or combination product engineering, with at least 5 years in a ... + Demonstrated technical leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing, assembly, and… more
- Merck (Rahway, NJ)
- …and support of Autoinjectors. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, and ... a minimum of 20 years of hands-on experience in medical device engineering, with a focus on...such as ISO, USP, FDA guidelines, and other global regulatory standards pertaining to medical devices and… more
- Merck (Rahway, NJ)
- …and Skills: . **Manufacturing** - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination Products. ... and compliance requirements governing development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU Medical Device … more
- Sanofi Group (Morristown, NJ)
- …and bring hope to patients and their families. The strategic vision of Sanofi's Global Medical Device and Packaging organization is to lead the industry in ... market auto-injectors, pens, safety syringes, as well as connected medical device technologies, and we are gearing...validation plan and execution of IQ/OQ/PQ in accordance with regulatory , company & site requirements. Will often support sites… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …experience in clinical investigation + Minimum of 10 years experience in the Medical Device /In Vitro Diagnostics industry required. More than six (6) years ... We are **the makers of possible** ! BD is one of the largest global medical technology companies in the world. _Advancing the world of health_ (TM) is our Purpose,… more
- J&J Family of Companies (Raritan, NJ)
- …enabling robust GxP Quality Management System of a diverse portfolio of drug and medical device health products and services. This individual serves as the ... to ensure quality of the GxP system, compliance with regulatory requirements and SOPs, and to ensure a continued...field and/or equivalent time and experience in a related medical device R&D area + Good understanding… more
- Terumo Medical Corporation (Somerset, NJ)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Additionally, they will stay updated on the SUT/CAD VAT rules within the medical device industry for multiple jurisdictions. This individual will establish… more
- Merck (Rahway, NJ)
- …and Qualifications:** + Minimum of 10 years' experience in the pharmaceutical, biotechnology, or medical device industry, with at least 3-5 years in a leadership ... equipment design, development and qualification. + Strong background in the medical device , combination product, pharmaceutical packaging equipment and… more