Assurance Engineer on our Acute Care Technology Research and Development (R&D) team, this role will perform electronic test... products Design and test to meet FDA/IEC standards and develop test techniques Document test systems planning, architecture...
Overview: The R&D Manager, Capital Equipment will be responsible for overseeing R&D project team(s) in the execution... and business needs are appropriately addressed. Technical responsibility for all R&D activities assigned. Identifying new vendors...
requirements. Supervises Assistant Controller, Accounts Payable and A/R Accounting Staff and Financial Analysts. Oversees...-Owned Business Enterprise, ISO/IEC 27001, SOC 2 Type 2 certified company with massive 18+years of diversified...
with family of standards for electrical safety of medical devices IEC/EN/UL 60601-1 Experience in R&D environment, delivering...
Construction, R&D, Risk, Legal, TES, Social Responsibility, Sustainability, TOM, and Fleet. The role's scale will include... or construction management. Working knowledge of” ISO, IEC, or regulatory requirements or standards, etc. Have or working towards a PE...
in a role which required knowledge of MIL-STD-704, MIL-STD-1275, MIL-STD-461, MIL-STD-464, DO-160, IEC-61000, and/or FCC part 15... control compliance requirements, a “U.S. Person” as defined by 22 C.F.R. §120.15 is required. “U.S. Person” includes...
with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The Core R..., ISO/TS 10974, IEC 60601-2-33, etc. Work under minimal supervision Ensure understanding of all quality policy/system...
Overview The R&D Manager, Capital Equipment will be responsible for overseeing R&D project team(s) in the execution... and business needs are appropriately addressed. Technical responsibility for all R&D activities assigned. Identifying new vendors...
for QA-related R&D activities from research through product launch. This position ensures that design controls and risk... of regulatory and international standards requirements including 21 CFR 820, ISO 13485, ISO 14971 and IEC 62304 to support quality...
+ years industry experience Quality Assurance, R&D, or Regulatory Affairs in Medical Device or Pharmaceutical Industries.... Experience with Medical Device Quality Systems (21 CFR 820, ISO-13485, and EU MDR) Strong familiarity with ISO-14971 and IEC...