Process Engineer II - cGMP Med Devices & Improvement

A leading medical device company is looking for a Process Engineer II in Bedford, MA. This position supports process improvement for medical devices and drug products by designing and implementing systems ensuring cGMP compliance. Responsibilities include collaborating with suppliers, conducting process validations, and training staff. Ideal candidates will have a Bachelor's degree in Chemical or Mechanical Engineering, along with 2-5 years of experience in a regulated environment.

Strong troubleshooting and communication skills are essential. Competitive salary with robust benefits offered.
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