- Fujifilm (Wayne, NJ)
- …and procedures. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... or degree preferred, but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field. + Soldering experience… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …technical field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with ... ISO frameworks, GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to align technical decisions… more
- ManpowerGroup (Princeton, NJ)
- Our client, a leader in the medical device industry, is seeking a Product Support Specialist Sr. II to join their team. As a Product Support Specialist Sr. II, ... medically-related field. + 3-5 years of experience in an FDA regulated environment. + Ability to assimilate complex technical...your skills in troubleshooting and technical support within the medical device industry. + Collaborate with a… more
- Fujifilm (Trenton, NJ)
- …United States. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...evolving situations and needs + Strong commitment to delivering high- quality work and upholding HCUS values. + Proficiency in… more
- Fujifilm (Trenton, NJ)
- …and II + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...Provides on-going support to resolve application related and image quality concerns on both a product and system level.… more
- Fujifilm (Trenton, NJ)
- …management. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …products by closely working with MTP internal colleagues in various functions ( Quality Assurance, Regulatory Affairs, Marketing, Market Access, Medical Affairs, ... respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several… more
- Fujifilm (Wayne, NJ)
- …exceed deadlines. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard ... **Position Overview** This position is responsible for technical repair and final quality inspection on assigned Endoscopic units. This position is responsible for… more
- Bristol Myers Squibb (Princeton, NJ)
- …of industry experience in bioanalysis and/or IVD/CDx development within pharmaceutical, biotech, medical device , or CRO settings. + Direct experience managing ... excellence for regulated bioanalytical studies and CDx development, ensuring high quality , compliance, and timely delivery of internal and outsourced projects. This… more
- Integra LifeSciences (Princeton, NJ)
- …Legal, and Operations to ensure alignment across product lifecycle phases and compliance with medical device regulations (eg, FDA , ISO 13485, MDR). Ensure ... procurement strategy aligned with corporate goals, emphasizing cost reduction, supplier quality , risk mitigation, and innovation. + Establish and maintain strategic… more