- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …Science background is preferred. Specialist : 3+ years in regulatory affairs, medical device /IVD industry required. 3+ years in FDA environment preferred. ... appropriately translated into the quality management system. This position may require support from senior Regulatory Affairs members and/or managers. This role can… more
- Abbott (St. Paul, MN)
- …or CEPS certification; or, Design Validation and GLP study experience in the medical device industry. + Demonstrated ability to apply an expert understanding ... including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. Medical device industry experience preferred. Training and experience… more
- Aston Carter (Burnsville, MN)
- …field. + Minimum 5 years of supply chain experience, ideally in complex medical device manufacturing. + Proven experience in purchasing, planning, and ... at the forefront of cardiac care innovation. As a Supply Chain Specialist , you'll be instrumental in scaling our manufacturing capabilities by refining processes… more
- Envista Holdings Corporation (New Orleans, LA)
- …allowance and mileage reimbursed through Motus **Preferred Requirements:** + Medical device /technical sales experience; regenerative/biologics or dental implants ... **Job Description:** The **Regenerative Sales Specialist ** is responsible for achieving or exceeding sales and service goals mainly in dental clinics, universities… more
- Cardinal Health (Indianapolis, IN)
- …working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device ) preferred. + Has experience in authoring a variety of forms ... difference for our customers and communities. **What a Senior Specialist , Quality Control (Chemistry) contributes to Cardinal Health** Quality...offers a wide variety of benefits and programs to support health and well-being. + Medical , dental… more
- Danaher Corporation (Sunnyvale, CA)
- …(IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) participating regulatory authorities ... (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Quality Systems Specialist is responsible for functioning as Lead Internal Auditor… more
- CosignMed (El Paso, TX)
- Clinical Specialist El Paso, TX + Apply + + View...Certified Medical Technician + Two years of medical device or Operating Room experience, preferred + ... Men's Health surgical procedures as requested on prn basis + Providing technical support to physicians, surgical staff and institutions + Confirm case details with… more
- ThermoFisher Scientific (Rochester, NY)
- …least 2 years of experience in a regulated industry (pharmaceutical or medical device ). **Preferred Qualifications** + Familiarity with product stewardship, ... regulations (EU REACH, CA Prop 65, TSCA). + Understanding of pharmaceutical and medical device standards and regulations (USP, ISO 10993, ISO 13485, IVDR,… more
- Achieve Beyond (Forest Hills, NY)
- LMSW Early Intervention Evaluations Specialist Apply Now! Back to search Location: Forest Hills, New York Department: Administrative Posted: 10/10/2025 Location ... have potential. We are guided by the mission to support children with special needs to Achieve Beyond their...to 90% of the workday working on a computer/electronic device . + The ability to observe details at close… more
- ThermoFisher Scientific (Pittsburgh, PA)
- …manufacturing and/or supply chain experience is preferred + Experience in life sciences, medical device , or pharmaceutical industries is a plus **Benefits:** We ... solutions for major challenges. How will you make an impact? The UFM Program Specialist is essential for the success and longevity of the UFM program in North… more