At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director to join our Regulatory Sciences team, to turn strategy into execution. Someone who is operationally minded, enjoys building and improving processes, develops high-performing teams, and isn't afraid to roll up their sleeves to remove roadblocks and drive results.
When & where:- Location: Troy, New York, United States
- Work model: Monday - Friday 8am - 4:30pm
- Lead and manage a team responsible for authoring and coordinating CMC regulatory submissions across all modalities — biologics, small molecule, cell and gene therapy, and combination products — from IND/CTA through NDA/BLA and post-approval lifecycle
- Develop and implement global CMC regulatory strategies for product development and lifecycle management, aligning with business objectives and accelerating time to approval
- Build and continuously improve team processes, templates, workflows, and submission tracking systems to increase throughput and consistency, enabling the team to reliably meet aggressive and shifting timelines
- Establish and track operational metrics such as cycle time, submission quality, and on-time delivery to identify bottlenecks and drive measurable improvements in team efficiency
- Manage team capacity and workload distribution across concurrent submissions, proactively identifying resourcing gaps and reallocating support during peak submission periods
- Mentor, coach, and develop staff to build bench strength and technical capability; represent the company in industry professional associations to help shape the external regulatory environment
- Demonstrated experience managing or leading a team with a track record of developing talent and scaling team output
- Strong working knowledge of FDA, EMA, and international CMC regulations and guidance across multiple modalities
- BS/BA in a life sciences discipline required
- Associate Director: 10+ years of experience in the healthcare or biotech industry
- Director: 12+ years of experience in the healthcare or biotech industry
- Senior Director: 15+ years of experience in the healthcare or biotech industry
- May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role
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)
$147,800.00 - $338,400.00Skills Required
- BS/BA in a life sciences discipline
- 12+ years of experience in the healthcare or biotech industry (Director level)
- Strong working knowledge of FDA, EMA, and international CMC regulations and guidance across multiple modalities
- Demonstrated experience managing or leading a team and developing talent
- Experience authoring and coordinating CMC regulatory submissions from IND/CTA through NDA/BLA and post-approval
- Ability to interact directly with regulatory authorities and represent CMC strategy
- Experience building and improving team processes, templates, workflows, and submission tracking systems
- Willingness to work on-site in Troy, New York per stated schedule (Monday-Friday)
Regeneron Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Regeneron and has not been reviewed or approved by Regeneron.
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Healthcare Strength — Medical, dental, and vision coverage is positioned as comprehensive, with Regeneron prescription drugs covered at 100% for those enrolled in the medical plan. Mental health support is also emphasized through EAP access and tools like Talkspace and the Journey app.
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Equity Value & Accessibility — Stock grants are described as available to all employees, strengthening the overall total-rewards package beyond base pay. Long-term incentives and stock-related rewards are repeatedly framed as meaningful components of compensation.
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Parental & Family Support — Paid parental leave is paired with fertility/adoption assistance and childcare-related support such as discounts and nanny services. Additional family-oriented resources extend to elder care, pet care, and education support like college coaching and tutoring.
Regeneron Insights
What We Do
At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in. Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media. An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.









