- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + Strong knowledge of current global Good ... and follow-up of internal and external audits to ensure compliance with regulatory requirements. + ** Regulatory...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
- Integra LifeSciences (Plainsboro, NJ)
- … Medical Device Directive, Canadian Medical Device Regulations, and other applicable regulatory agencies/ requirements. **SUPERVISION EXERCISED** ... and evaluates the activities of associates in the Product Release group ,including, Device History Record (DHR) review, final review and release of finished product,… more
- J&J Family of Companies (Raritan, NJ)
- … medical device industry + Good working knowledge and understanding of medical device regulations, standards, and regulatory bodies, eg FDA (Food and ... other SOPs, balancing flexibility, efficiency, and speed, while adhering to applicable medical device industry regulations. This person will represent R&D for… more
- Astrix Technology (Somerset County, NJ)
- …validation, and optimization for medical and surgical products + Ensure compliance with quality and regulatory standards + Collaborate with R&D, ... - 19/02/2025 Apply for Job Our client who is a global, Fortune 100 Medical Device company is seeking a Process Engineer to join their team in Somerset Count,… more
- Bausch + Lomb (Trenton, NJ)
- …departments (eg, R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device ... clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical data management. + Minimum 10-12… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …(eg, presentations/publications focused on surgical device modeling, ISPOR Surgery or Medical Device SIG). + Has substantial hands-on experience planning and ... and guide product strategy -- May include cross-functional collaboration with R&D, Medical Affairs, Market Access, Regulatory Affairs and Marketing + Interact… more
- Bristol Myers Squibb (Princeton, NJ)
- …As Low as Reasonably Achievable (ALARA), are effective, and within BMS and regulatory compliance . + Maintain liaison with Facilities, Engineering, and R&D ... program. Including specialized training for Cyclotron operators and radiochemists, x-ray device users, preclinical imaging, radiochemistry suite, medical staff,… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …BS/BAOR + 6+ Years with MS/MA or MBA **Preferred Qualifications** * 6+ years Medical Affairs ( medical device /pharmaceutical industry), managed care, and HEOR ... institutions and/or hospitals strongly preferred * Solid working knowledge of regulatory and compliance environment * Effective organizational, project planning,… more
- Integra LifeSciences (Plainsboro, NJ)
- …all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for ... and set new standards of care. The **Supervisor, Automated Medical Operations** is responsible for the medical ...minimum costs, prevent operational delays, and maintain quality and regulatory compliance standards. + Trains and ensures… more
- BD (Becton, Dickinson and Company) (Branchburg, NJ)
- … testing + Knowledge of method development, validation, and regulatory compliance + Deep understanding of drug- device development, design control, and system ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...and capacity planning. + Drives continuous improvement, efficiency, and compliance with all applicable regulatory and quality… more