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EU MDR Remote Jobs

9 fresh jobs found

Customer Quality Manager - Recalls and Device Tracking
US Remote, United States

Device tracking 21 CFR 806 21 CFR 821 Recall management 21 CFR 820 EU MDR Medical Device Regulations Medical device industry ISO 13485 +17

Senior Mid Full Time

USD 125K+

Principal Scientist, Device Product and Process Development (Director Equivalent)
USA - New Jersey - Rahway, United States

Risk-oriented development Structural finite element analysis Measurement techniques Design failure modes and effects analysis In silico modeling Device characterization FDA guidance Device technology Mechanical Testing +70

Senior Full Time

USD 153K+

Manager, Quality Systems & Compliance - Purchasing Controls - Remote
USA - New Jersey - Rahway, United States

Medical device standards Supplier Audits Purchasing controls Deviations Document management systems Quality Risk Management QMS EU MDR Current good manufacturing practices +66

USD 94K+

Sr./Director, Quality Assurance
Virtual US

Cleerly Remote-first

21 CFR 801 21 CFR 803 Docs Slides 21 CFR 820 MDSAP EU MDR Regulatory strategy Sheets +30

Senior Full Time

USD 210K+

Associate Director, Quality Assurance - Remote
USA - New Jersey - Rahway, United States

Purchasing controls Preventive action 21cfr820 ICH Q9 21cfr part 4 Combination product development Design Controls Good manufacturing practice Device development +76

Senior Mid Full Time

USD 139K+

Manager, Clinical Science/Medical Writing
USA-California-Remote, United States

Edwards Lifesciences

Clinical protocol development Clinical writing Clinical Affairs EU MDR Clinical study design Clinical Study Reports Literature review Clinical evaluation Protocol Development +25

Senior Full Time

USD 120K+

Product Security Risk Analyst (Remote)
Michigan, Virtual Address, United States

IEC 81001-5-1 UL-2900 GRC platforms Nist rmf EU MDR OneTrust Medical Device Regulations Product Lifecycle Product Security +34

Entry Mid Full Time

USD 100K+

Clinical Study Manager (Remote)
Michigan, Portage 3800 East Centre Ave, United States

Medical Device Experience Clinical Trial Management Systems (CTMS) Electronic Trial Master File (eTMF) Clinical Evidence Strategy Good Clinical Practice (GCP) Publication strategy EU MDR Clinical evaluations Clinical evaluation +39

Senior Mid Full Time

USD 87K+

Staff Product Security Analyst
Remote US

Medical Device Design Software bill of materials Product security policy documentation Medical device security EU MDR FDA compliance Data Flow Diagrams Secure coding Threat modeling +22

Senior Full Time

USD 150K+

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