Quick Overview
Seniority
Mid Senior
Work mode
Hybrid
Location
Arvada, CO, United States
Posted
21 hours ago
Job Description
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 preferred.
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