KARL STORZ North America is seeking a collaborative Quality Engineer to support medical device development. You will partner with project teams to ensure regulatory compliance, patient safety, and product quality throughout the lifecycle.
Responsibilities include managing DHF/DMR, supporting design reviews, and driving continuous improvement. Ideal candidates hold a degree in engineering or life sciences and have 2–4 years in a regulated environment with strong communication skills.
Matching similar jobs
Level
Lead L6
Location
Charlton, MA
Occupation
Validation Engineers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
