- L'Oreal USA (Clark, NJ)
- …relevant product safety experience in the cosmetic, OTC, consumer health care, medical device , dietary supplements, and/or pharmaceutical industries, with global ... of SRCM Americas with regards to cosmetics, OTC monograph products, drugs, medical devices and chemicals throughout the product lifecycle. + Lead and develop… more
- Grifols Shared Services North America, Inc (Trenton, NJ)
- …submissions. + May supervise staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams ... strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides regulatory expertise… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …to successfully deliver the product development outcomes. + High volume disposable medical device product development experience from concept to successful ... and mitigate risk points. Make tradeoffs between time, schedule, cost, and quality (when appropriate), while meeting safety and regulatory requirements + Exhibit… more
- Sokol Materials & Services (Skillman, NJ)
- …experience in CQV and/or CSV within the pharmaceutical, biotechnology, cell therapy or medical device industries. + Experience with Cell Therapy equipment (cell ... including risk-based validation approaches. + Knowledge of regulatory requirements, including FDA , EMA, and ICH guidelines. Knowledge, Skills & Abilities: +… more
- Integra LifeSciences (Princeton, NJ)
- …Oracle + Experience in a multi-national manufacturing and distribution organization, medical device or pharmaceutical industry preferred Integra LifeSciences is ... full compliance with US Customs and Border Protection (CBP), FDA , and other government agency regulations for both imports...and leadership skills + Proven attention to detail and quality is mandatory + US Customs brokerage license preferred… more
- Sokol Materials & Services (Skillman, NJ)
- …Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and ... Strong understanding of validation principles, methodologies, and regulatory requirements, including FDA , EMA, and ICH guidelines. Knowledge, Skills & Abilities: +… more