Arvada, Colorado
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Today
Skills Required: Program management, manufacturing transfer, medical device compliance, ISO 13485, FDA 21 CFR Part 820, EU MDR, GMP, IQ/OQ/PQ, process validation, risk management, and Microsoft Project. Experience: Strong leadership in medical device manufacturing transfers, preferably sterile disposable devices. Must manage cross-functional teams, BOMs, process documentation, supply continuity, validation, budgets, risks, and executive reporting. PMP, Lean Manufacturing, and Six Sigma are prefe
Easy Apply
Full-time
35 - 40