Global Regulatory Affairs Lead – GMP & Submissions
Listed on 2026-10-06
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Englewood Lab, Inc. is seeking a Regulatory Affairs Manager to lead regulatory operations at our Totowa, NJ site, ensuring alignment with global regulatory strategy and quality standards.
You will oversee regulatory compliance, submissions, and facility registrations while coordinating cross-functionally to support audits and regulatory programs. Strong FDA knowledge and leadership are essential.
This opening is for the Global Regulatory Affairs Lead – GMP & Submissions role at Englewood Lab, Inc.
The advertised compensation is 90..
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 Global Regulatory Affairs Lead – GMP & Submissions role in the description above.
We appreciate your interest in this position.
Join Englewood Lab, Inc. and contribute to our ongoing work.
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