- Merck & Co. (Rahway, NJ)
- …guidance & standards: 21 CFR Part 421 CFR 82021 CFR 210/ 211EU Medical Device RegulationUSP USP FDA Guidance for Industry, Container Closure Systems ... Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical… more
- Cognizant (Highland Heights, KY)
- **About the role** As an ** Instrument & Medical Device Validation Specialist** , you will make an impact by ensuring software installed on laboratory ... have to be considered:** . Extensive experience in instrument or medical device validation within a regulated (GxP) environment. . Strong technical… more
- Cognizant (Highland Heights, KY)
- …accordance with EMA guidelines. The ideal candidate will have strong Instrument / Medical device validation experience and will be crucial to ensure ... considered:** + **8+ years of extensive experience in instrument or medical device validation within a regulated (GxP) environment.** + Strong technical… more
- Cognizant (Highland Heights, KY)
- **About the role** As an ** Instrument / Medical Device Validation Specialist** , you will make an impact by ensuring software installed on laboratory ... you need to have to be considered** + 6-10+ years of experience in Instrument / Medical Device validation within a regulated (GxP) environment. + Strong… more
- Cognizant (Highland Heights, KY)
- …**What you need to have to be considered** + 6-10+ years of experience in Instrument / Medical Device validation within a regulated (GxP) environment. + ... **About the role** As an ** Validation Specialist - Medical Devices &...with EMA guidelines and IT SOPs in pharmaceutical or medical device settings. + Experience with risk… more
- CBRE (Indianapolis, IN)
- Process Instrument Technician Job ID 237928 Posted 22-Oct-2025 Service line GWS Segment Role type Full-time Areas of Interest Building Management, ... DO2 Transmitters, Pressure and Temperature controllers, Delta V Foundation Field bus, Device Net, PLC controlled devices and all related data and communication… more
- DEKA Research & Development (Manchester, NH)
- …for a Verification and Validation Test Engineer to work in a dynamic medical device R&D environment. Test Engineering is a high-visibility role with a ... you will make an impact as a Verification and Validation Test Engineer: + Developing and writing test procedures...Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred About DEKA:… more
- Danaher Corporation (Washington, DC)
- …processes, especially for medical devices and AI/ML-based software as a medical device (SaMD). + Familiarity with quality management systems and standards ... about the Danaher Business System which makes everything possible. The AI Evaluation Engineer, Device Intelligence will be a key member of the AI Product and Imaging… more
- Merck (Rahway, NJ)
- …& standards:** + 21 CFR Part 4 + 21 CFR 820 + 21 CFR 210/ 211 + EU Medical Device Regulation + USP <1> + USP <697> + FDA Guidance for Industry, Container Closure ... Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Microscopies, Negotiation, Optical… more
- Unither Pharmaceuticals (Rochester, NY)
- …needed Laboratory or analytical development experience in pharmaceutical manufacturing or medical device background required SPECIFIC SKILLS: Must have previous ... in cGMP environment Knowledge of LIMS use and development Strong knowledge in instrument and software validation Ability to evaluate data, perform trend… more
- Hologic (San Diego, CA)
- …a leadership role requiring a proven level of technical expertise, ideally within Medical Device and Diagnostics space, and a successful cross-functional leader ... evaluation methods, labeling per 21 CFR 809). + Oversee instrument /cartridge verification and validation (including wet bench), environmental/EMC/safety… more
- Teradyne (Agoura Hills, CA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... and embedded algorithms for Digital, DC, AC & RF instrument calibration in the ATE equipment using C/C++/C# and...development of HW error budget and offline & online validation of these error terms using statistical analysis techniques… more
- Veterans Affairs, Veterans Health Administration (Albuquerque, NM)
- …for safety and prevention of cross contamination.2. Basic knowledge of medical terminology to assemble specialty operating room/clinic instrument sets.3. ... Summary The New Mexico VA Healthcare Network is recruiting for a Medical Supply Technician assigned to Sterile Processing service (SPS). PLEASE NOTE: This job… more
- Keurig Dr Pepper (Williamson, NY)
- …Luminescence System, UV-Vis, etc. + Must be adept at determining that each instrument or device performs within the specified operational parameters. + ... and existing laboratory staff to new procedures and techniques + Conduct instrument and method development, perform validation programs on new processes… more
- Zimmer Biomet (Englewood, CO)
- …design control activities and verification and validation activities with respect to medical device development. + Understanding of medical device ... Parametric modeling and detail design of P28 implant and instrument development with a firm grasp on design for...with 6+ years of experience + Prior experience in medical device development required. + Prior experience… more
- Novant Health (NC)
- …seeking a Senior MDI System Administrator to lead the operational management of our Medical Device Integration (MDI) systems. This role is critical to ensuring ... integration and connectivity problems. + Ensure proper testing and validation of new device integrations. + Maintain...Epic, Cerner, or other EMR platforms. + Knowledge of medical device standards and regulatory compliance. +… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …21CFR820 Quality System Regulation + 21CFR11 Electronic Records requirements + ISO 13485 Medical Device Quality Management + ISO 14971 Risk Management protocols ... or transferred products to administer the design control and validation elements of the Quality System to ensure regulatory...of industry standard quality practices and tools to the Instrument Plant and it's suppliers. **Job Description** We are… more
- Microsoft Corporation (Redmond, WA)
- …quantum hardware roadmap and requires deep expertise in semiconductor physics, device fabrication, and crystal chemistry. The successful candidate will lead efforts ... in designing robust test structures, and evaluating device performance across cryogenic and room temperatures. You will apply advanced statistical analysis and data… more
- Abbott (San Diego, CA)
- …level of quality, compliance, and adequate documentation is applied to every medical instrument which undergoes the refurbishment/repair process. **2nd Shift: ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Oct 10, 2025 Req ID: 4974 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: PM&PD Management Terumo Medical Corporation (TMC) develops,… more
