
Manager Combination Products - Regulatory Affairs
Rensselaer, NYJob$108–176K/yrSeen 1w agoSeen in employer's feed 2 days ago
Most applications go out cold — see where you stand first. No sign-up to start.
Watch jobs like this. New roles like this one near Rensselaer, NY, by email.
Don't just apply. Show up ready.
Olive works from this exact posting.
At a glance
Olive lists jobs from US employers, including remote roles you can work from the United States.
Job overview
Regeneron seeks a Manager, Regulatory Affairs - Combination Products, to support global combination product development, regulatory submissions, and post-market activities. The role collaborates with Regulatory Affairs, Manufacturing, Quality, and other stakeholders, and supports work from early development through post-market activities. It is based onsite in Rensselaer, New York, five days per week.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
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 Manager, Regulatory Affairs - Combination Products to join our Regulatory Affairs team, supporting our combination product business area in an onsite work model. In this role, you will support global combination product development, regulatory submissions, and post-market activities while collaborating with Regulatory Affairs, Manufacturing, Quality, and combination product stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide .
When & where:
Rensselaer, New York
Work model: Onsite, 5 days per week
Discover your role:
• Support combination product development from early phase through post-market activities.
-
Review regulatory filings including INDs, BLAs, MAAs, annual reports, and supplements.
-
Develop design control documentation and quality systems for combination products.
-
Assess changes and deviations for regulatory impact and submission requirements.
-
Support regulatory authority meetings, responses, and inspections.
-
Create SOPs, Working Instructions, and Reviewer’s Guides.
-
Identify process gaps and support regulatory intelligence activities.
-
You translate ambiguity into action and build effective stakeholder partnerships.
This role requires:
-
Bachelor’s degree with 6+ years related experience, or advanced degree with 3+ years related experience in pharmaceutical or biotechnology, settings.
-
2-4 years of CMC Regulatory Affairs experience supporting worldwide regulations.
-
Strong understanding of global CMC Regulatory Affairs requirements, including combination products and human factors.
-
Experience delivering marketing authorizations, CTA/INDs, and post-approval submissions.
-
Experience supporting biologics and combination products preferred.
-
Experience engaging with FDA or other regulatory authorities preferred.
-
Ability to assess regulatory impact, support compliance activities, and mentor junior staff.
-
Strong communication, negotiation, strategic thinking, problem-solving, prioritization, and cross-functional collaboration skills.
-
Ability to support training activities and proactively address technical or regulatory knowledge gaps.
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: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. 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.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. 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)
$108,000.00 - $176,000.00
How this job compares
Set against the 944 open Regulatory Affairs jobs on Olive Jobs, counted October 27, 2026.
- Pay
- This posting$108–176K/yr
- New York median$120–179K/yr39 salary ranges
- US median$142–197K/yr668 salary ranges
This range's midpoint, $142K, is close to the New York median midpoint ($145K) — in the middle half of Regulatory Affairs salary ranges in New York.
- Openings
- Olive Jobs lists 52 open Regulatory Affairs jobs in New York and 944 across the US. 11% of them nationwide are listed as remote or flexible.
- Hiring the most in New York
- Regeneron Pharmaceuticals (this employer)8 open
- Google3 open
- NYU Langone Medical Center3 open
- Experience
- This posting asks for at least 3 years of experience — less than three in four Regulatory Affairs postings that state a minimum ask for (median 7 years, across 806 postings).
- Education
- 583 of the 944 open Regulatory Affairs jobs (62%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on October 27, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
Similar jobs, posted recently
Open roles like this one, listed in the last 30 days.
Manager, CMC Regulatory Affairs - BiologicsRegeneron Pharmaceuticals · Rensselaer, NY · $108–176K/yr
Manager CMC Regulatory AffairsRegeneron Pharmaceuticals · Rensselaer, NY · $108–176K/yr
Senior Specialist, CMC Regulatory Affairs - Quality ComplianceRegeneron Pharmaceuticals · Troy, NY · $79–129K/yr
CMC Product Quality Compliance Specialist, PQRRegeneron Pharmaceuticals · Troy, NY · $67–110K/yr
Senior Manager Clean EnvironmentsRegeneron Pharmaceuticals · Rensselaer, NY · $126–206K/yr
You've read the whole posting — now see how you match it.