- Capgemini (Bridgewater, NJ)
- … management + Strongunderstanding of clinical trial operations, regulatory compliance, anddata privacy. + Excellentcommunication, stakeholder engagement, and ... systems. This includes working closely with cross-functional teams, aligning with regulatory and compliance standards, and ensuring timely delivery of milestones… more
- Fresenius Medical Center (Cherry Hill, NJ)
- …equipment and technology, including but not limited to, patient monitors, defibrillators, medical recording devices , sterilizers and computers in a safe and ... Adheres to the Organization Compliance Program, including following all regulatory and Organization policy requirements. Provides direct nursing care pre,… more
- ManpowerGroup (Wayne, NJ)
- …Engineer **Location:** Wayne, NJ **Pay Rate:** $50 per hour Our client, a leading medical device company, is seeking a **Quality Engineer II** to join their ... This critical role ensures the quality and compliance of medical devices throughout the product development lifecycle....of experience in Quality or Engineering, preferably in the medical device or pharmaceutical industry. + Experience… more
- Cognizant (Trenton, NJ)
- …**Opcenter Technical:** A dynamic professional with proven expertise in Siemens Opcenter Medical Devices / Camstar application in Manufacturing Execution domain. ... cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the… more
- Integra LifeSciences (Princeton, NJ)
- …Engineer II with a focus on bacterial endotoxin testing programs in the medical device industry. The successful candidate will be responsible for partnering ... a willingness to learn about bacterial endotoxin testing programs, an understanding of medical device quality systems, and a commitment to ensuring product… more
- IQVIA (Parsippany, NJ)
- …+ 2-years or more experience in training and education in the pharmaceutical or medical device industry, or equivalent experience required + The ability to ... events, and reinforcement training activities + Consults and collaborates with client medical , commercial, and regulatory leadership, as well as IQVIA program… more
- J&J Family of Companies (Raritan, NJ)
- …equivalent experience is preferred. + Experience in a regulated industry ( medical device , biopharmaceutical, or pharmaceutical) + Experience leading ... Abilities:** + Knowledge of, and experience with, applicable standards and regulations in medical devices + Proven experience with the application of Design… 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
- embecta (Parsippany, NJ)
- …Quality Compliance Auditor is a critical role within embecta, a global leader in medical device manufacturing. This position ensures that all quality systems and ... operations comply with internal standards and regulatory requirements, including FDA and ISO standards. The Quality...in quality compliance or a related role within the Medical Device or Pharmaceutical manufacturing industry. +… 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