- Agiliti Health (Paterson, NJ)
- … equipment management experts who proudly serve hospitals and healthcare facilities to ensure quality medical equipment is in the right place at the right time ... repairs, preventive maintenance and calibration. + Participate in hazard identification and medical device reporting procedures. + Instruct customer personnel on… more
- Sanofi Group (Morristown, NJ)
- …or PhD in LifeScience; Law or Computer Sciences + **Pharmaceutical, biotech, medical device industry experience required** + Demonstrated experience in working ... to generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements, and… more
- Integra LifeSciences (Plainsboro, NJ)
- …the identity, quality , durability, reliability, safety, and effectiveness of medical devices and, thereby, protect patient safety. **ESSENTIAL DUTIES AND ... ensuring that they meet performance expectations and adhere to safety, quality , and regulatory standards. + Imparts a culture of 6S and continuous improvement… more
- Integra LifeSciences (Plainsboro, NJ)
- …+ 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience in a clean room ... records, required logs, books, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more
- Marotta Controls, Inc. (Montville, NJ)
- …Controls, a New Jersey Top Workplace three years running! Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the Aerospace ... (ie procedures, schematics/technical drawings, etc.) and use necessary measuring devices /equipment to confirm tooling/fixturing geometries and dimensions, as directed… more
- Integra LifeSciences (Plainsboro, NJ)
- …0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly ... required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more
- iconectiv (Bridgewater, NJ)
- …rely on our data exchange platforms each day to keep their networks, devices and applications connected and 2B consumers and businesses protected. Our cloud-based ... security for 3 rd party applications, host systems, development software, devices , and technologies for vulnerabilities; and developing requirements for related… more
- Fujifilm (Trenton, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- Integra LifeSciences (Plainsboro, NJ)
- …0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly ... required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more
- Integra LifeSciences (Plainsboro, NJ)
- …position. + High School diploma or equivalent. + 0-2 years working in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly ... accurate records, required logs and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more