Senior Manufacturing Validation Engineer; MedTech/Regulated
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Engineering
Job Description & How to Apply Below
United Pharma seeks an experienced Validation Engineer to lead and execute manufacturing equipment validation in a regulated environment. You will collaborate with cross-functional teams to draft, review, and release IQ/OQ/PQ documents, and ensure compliance with ISO 13485, GMP, and 21 CFR Part 820.
The role emphasizes metrology, calibration, MSA, and robust documentation practices. Responsibilities include coordinating validation activities from vendor selection to commissioning, releasing
The Senior Manufacturing Validation Engineer (Med Tech/Regulated) role at United Pharma is now open for applications in MA, United States.
The advertised compensation is 110..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Senior Manufacturing Validation Engineer (Med Tech/Regulated) role in the description above.
We appreciate your interest in this position.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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