Sanofi Inc. in Cambridge, MA is seeking a Device Quality Engineer to lead risk management, clinical evaluation, and post-market surveillance across the global device portfolio.
You will ensure compliance with ISO 14971, MDR, and related regulatory requirements throughout the product lifecycle. You will partner with quality, compliance, development, and manufacturing teams to deliver expert evaluations, drive improvements, and mentor colleagues in risk management methodologies while supporting
#J-18808-LjbffrGlobal Device Risk & Post-Market Quality Engineer in cambridge at Unknown Company
This position is listed as full time and onsite.