- Zimmer Biomet (Parsippany, NJ)
- …year of relevant work experience. 3-5 years of experience preferred. + Certified Quality Engineer (CQE) and Medical Device , particularly Orthopedic Industry ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...and experts outside Zimmer Biomet to implement Zimmer Biomet quality goals. + Supplier Qualification + Supplier Corrective Action… more
- Zimmer Biomet (Fair Lawn, NJ)
- …**Your Background** + BS in Engineering. + Experience in the role + Certified Quality Engineer (CQE) and Medical device , particularly Orthopedic industry, ... innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's...and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. **How You'll Create Impact** + Individual will… more
- Integra LifeSciences (Princeton, NJ)
- …mindset, a willingness to learn about bacterial endotoxin testing programs, an understanding of medical device quality systems, and a commitment to ensuring ... Engineer II with a focus on bacterial endotoxin testing programs in the medical device industry. The successful candidate will be responsible for partnering… more
- Stryker (Mahwah, NJ)
- …Solving** : Research, design, develop, modify, and verify mechanical components for medical devices ; translate design inputs into engineering specifications; and ... + Minimum 4+ years of product design experience in orthopaedics or the medical device industry **Preferred Qualification** + Experience in the function, clinical… more
- Actalent (Emerson, NJ)
- …as calipers and micrometers. + Quality Assurance experience, preferably in medical devices , though experience in pharmaceuticals is also considered. + ... Job Title: Quality Control Laboratory TechnicianJob Description As a ...concerns and coordinating necessary repairs or rework. + Support regulatory compliance efforts by preparing documentation and maintaining relevant… 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
- 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 (Plainsboro, NJ)
- …overseeing the quality control inspection activities to ensure the safety, efficacy, and quality of the company's medical devices . This role is expected ... to provide technical and supervisory leadership and mentoring to the quality control inspectors and provides support to management. This job is expected to work… 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
- Bausch + Lomb (Trenton, NJ)
- …Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and Clinical ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more