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Compliance Specialist (External Manufacturing)
Compliance Specialist (External Manufacturing)-March 2024
East Greenbush
Mar 29, 2026
About Compliance Specialist (External Manufacturing)

  We are currently looking to fill a Compliance Specialist, External Manufacturing position. This position is a member of the External Manufacturing Team and is responsible for operations support and compliance related activities for the manufacture of Regeneron products.

  In this role, a typical day might include the following:

  Leading and handling deviation investigations, CAPAs, and change controls

  Reviewing and maintaining procedures, polices and other instructional documents with a focus on continuous improvement

  Generating and tracking performance metrics

  Maintaining knowledge of current good manufacturing practices (cGMPs)

  Conducting periodic reviews of Drug Product Manufacturing documentation and records to assess for compliance with established quality standards, policies and procedures

  Maintaining required training status on Regeneron specific work instructions and SOPs

  Assisting in maintenance of product integrity and company reputation by assisting in the monitoring of cGMP compliance at drug product contract manufacturers

  Continuous Process Improvement Implementation

  This role may be for you if you:

  Have knowledge of drug product manufacturing from formulation through the final package

  Possess basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations

  Exhibit confidence, have a high emotional IQ, and have strong interpersonal, written and oral communication skills for providing team updates

  Like collaborating with external vendors and partners

  Enjoy travel to contract manufacturers or business partners, as the need arises (25% or less)

  To be considered for this role you must hold a Bachelor’s degree in scientific discipline and the following amount of related experience in cGMP manufacturing operations (clinical and/or commercial drug products) for each level:

  Associate Compliance Specialist: 0-2+ years

  Compliance Specialist: 2+ years

  May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.

  #REGNQA

  Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels!

  Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.

  The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

  Salary Range (annually)

  $58,480.40 - $106,300.00

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