Senior Quality Engineer - Medical Devices & Compliance
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Engineering
Job Description & How to Apply Below
Baxter is seeking a Principal Quality Engineer to provide strategic quality direction across complex manufacturing processes and product lifecycle activities. You will mentor engineers, lead investigations, and drive risk-based decisions to meet regulatory requirements and customer expectations.
The role requires advanced knowledge of FDA QSR, ISO 13485, ISO 14971, and cGMP, with experience in injection molding and multi-functional leadership. Competitive salary and benefits are offered.
The following position is for a Senior Quality Engineer
- Medical Devices & Compliance with Regulatory Toolkit.
We appreciate your interest in this position.
Join Regulatory Toolkit and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Senior Quality Engineer
- Medical Devices & Compliance role at Regulatory Toolkit, based in MN, United States.
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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