About this opportunity
Englewood Lab, Inc. lists this Global Regulatory Affairs Lead – GMP & Submissions opportunity in totowa, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
totowa, NJ, 07512, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.