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Regeneron Pharmaceuticals, Inc (USA) seeks a Senior Supply Chain Compliance Manager to lead a global compliance team across Supply Chain and Logistics, driving investigations, CAPAs, and change controls in a cGMP environment. You will collaborate with Quality, Regulatory and cross-functional partners to build a proactive compliance culture.
You will manage inspection readiness, develop training, and establish robust processes to ensure regulatory alignment and operational excellence across IOPS
Build our future together: At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Supply Chain Compliance Manager to join our IOPS Supply Chain and Logistics team, managing and overseeing all compliance-related activities — including investigations, change controls, and CAPA — across Supply Chain and Logistics operations at IOPS sites globally. In this role, you will lead and develop a compliance team, drive inspection readiness, and build a proactive compliance culture — while serving as a go-to technical mentor and collaborating with Quality, Regulatory, and cross‑functional partners across the organization. This position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.
Location: Troy, New York Work model: Monday - Friday 8am - 4:30pm, onsite Travel percentage: 25% to Ireland
Lead, develop, and guide a global team performing Supply Chain and Logistics compliance activities, fostering a healthy working environment where team members feel valued, respected, and accountable for results
Manage teams responsible for completing change controls, preparing investigation reports with root cause analysis, product impact assessments, and corrective action recommendations for medium and high severity non‑conformances
Oversee risk assessments and Failure Mode and Effects Analysis (FMEA) activities; ensure Corrective and Preventive Actions are appropriate, implemented as planned, and demonstrate intended effectiveness
Manage overall regulatory inspection preparation; oversee department liaisons during inspections and coordinate post‑inspection activities; drive proactive compliance through self‑audits, knowledge transfer, and compliance education
Develop and implement an effective compliance framework for Supply Chain and Logistics, including policies, procedures, best practice propagation, and SOP review and revision across all groups within the department
Track and trend compliance activities including investigations and CAPAs to identify improvement opportunities; ensure all training is maintained and documented in accordance with cGMP standards
Serve as the go‑to technical point of contact and mentor for compliance topics including investigations and inspections across the Supply Chain and Logistics team
Build and maintain a robust training program; provide support to groups and supervisors on the initiation, review, and follow‑up of CCs, NOEs, DNFs, impact statements, and corrective action plans
BS/BA degree with 8+ years of experience, or equivalent combination of education and experience; level determined based on qualifications
Experience in a cGMP environment required; pharmaceutical or biotechnology industry experience preferred
Advanced knowledge of cGMP operations, regulatory and quality requirements, root cause analysis, and risk evaluation methodologies
Working knowledge of quality systems and software applications such as QUMAS or similar
We are committed to building a workplace with an inclusive culture.
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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.
Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:
For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.
If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position. Salary Range (annually) $126,300.00 - $206,100.00
Regeneron is a leading biotechnology company that invents life‑transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.