Senior Level Regulatory Affairs Project Manager Jobs
Senior level regulatory affairs project manager jobs place experienced professionals in charge of regulatory strategy, submission timelines, and the cross-functional teams that deliver them. Roles are concentrated across Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Distribution & Wholesale, with a mix of on-site, hybrid, and remote positions available, and employers like Revolution Medicines, Revolution Medicines, and Insmed Incorporated hiring at this level now.
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At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Position Description:
The Advisor, CMC Regulatory Affairs – Biologicals for Elanco Animal Health is responsible for providing regulatory guidance resulting in comprehensive, cohesive, and compliant submissions and interactions to maintain product registrations and product availability. The individual in this role interacts with regulators and internal stakeholders to drive regulatory solutions.
The Advisor, CMC Regulatory Affairs – Biologicals will initiate strategies and follow-up on process improvements and commitments. Additionally, the individual in this role will focus on interacting positively while developing relationships with internal and external stakeholders including Manufacturing, Quality, R&D, and third party and trade association groups. The individual in this role is expected to perform key leadership responsibilities, which provide innovative solutions, a positive and motivating work environment, to ultimately deliver the Elanco pipeline and maintain established product registrations and regulatory availability.
Functions, Duties, Task:
Key Technical Responsibilities:
- Responsible for having a thorough understanding of the regulations to work independently within a cross-functional team.
- Anticipates and resolves complex problems to maintain product to market.
- Subject matter expertise to advise QC, QA, and Manufacturing on regulatory aspects.
- Ensure inspection readiness from regulatory perspective.
- Build tools, systems, and business processes to develop best capabilities.
- Writes and reviews submissions to ensure they are scientifically sound, accurate, and compliant in close collaboration with Subject Matter Experts.
- Coordinate, supervise and review commitment responses. Actively participates in meetings that drive strategy and outcomes.
Key Leadership Responsibilities:
- Proactively search for opportunities for continuous improvement and facilitate implementation of new standards and practices with the ability to think “out of the box”.
- Deliver regulatory solutions and opportunities while creating an innovative culture.
- Work effectively and flexibly within and across all Elanco teams, external collaborators, government agencies, and affiliates to assist in achieving overall Elanco deliverables.
- Create a positive, engaging, and inspiring work environment that is aligned with company objectives.
- Influence others to adopt a different view to create an innovative culture.
- Create an engaging culture and identify essential wins.
- Excellent interpersonal and communication skills.
Minimum Qualification (education, experience and/or training, required certifications):
- Master’s degree at a minimum
- Minimum 8 years in a veterinary vaccine / biological manufacturing setting
Additional Preferences:
- Strong understanding of varied regulatory requirements (e.g., US FDA, EMA, etc.) related to veterinary biological manufacturing.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
#LI-RH1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
At Elanco (NYSE: ELAN) – it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals’ lives better makes life better – join our team today!
Position Description:
The Advisor, CMC Regulatory Affairs – Biologicals for Elanco Animal Health is responsible for providing regulatory guidance resulting in comprehensive, cohesive, and compliant submissions and interactions to maintain product registrations and product availability. The individual in this role interacts with regulators and internal stakeholders to drive regulatory solutions.
The Advisor, CMC Regulatory Affairs – Biologicals will initiate strategies and follow-up on process improvements and commitments. Additionally, the individual in this role will focus on interacting positively while developing relationships with internal and external stakeholders including Manufacturing, Quality, R&D, and third party and trade association groups. The individual in this role is expected to perform key leadership responsibilities, which provide innovative solutions, a positive and motivating work environment, to ultimately deliver the Elanco pipeline and maintain established product registrations and regulatory availability.
Functions, Duties, Task:
Key Technical Responsibilities:
- Responsible for having a thorough understanding of the regulations to work independently within a cross-functional team.
- Anticipates and resolves complex problems to maintain product to market.
- Subject matter expertise to advise QC, QA, and Manufacturing on regulatory aspects.
- Ensure inspection readiness from regulatory perspective.
- Build tools, systems, and business processes to develop best capabilities.
- Writes and reviews submissions to ensure they are scientifically sound, accurate, and compliant in close collaboration with Subject Matter Experts.
- Coordinate, supervise and review commitment responses. Actively participates in meetings that drive strategy and outcomes.
Key Leadership Responsibilities:
- Proactively search for opportunities for continuous improvement and facilitate implementation of new standards and practices with the ability to think “out of the box”.
- Deliver regulatory solutions and opportunities while creating an innovative culture.
- Work effectively and flexibly within and across all Elanco teams, external collaborators, government agencies, and affiliates to assist in achieving overall Elanco deliverables.
- Create a positive, engaging, and inspiring work environment that is aligned with company objectives.
- Influence others to adopt a different view to create an innovative culture.
- Create an engaging culture and identify essential wins.
- Excellent interpersonal and communication skills.
Minimum Qualification (education, experience and/or training, required certifications):
- Master’s degree at a minimum
- Minimum 8 years in a veterinary vaccine / biological manufacturing setting
Additional Preferences:
- Strong understanding of varied regulatory requirements (e.g., US FDA, EMA, etc.) related to veterinary biological manufacturing.
Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
#LI-RH1
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
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Find JobsSenior Level Regulatory Affairs Project Manager Job Market
Who's Hiring
- Revolution Medicines22
- Insmed Incorporated3
- Insmed2
- Nurix Therapeutics2
Top Industries Hiring
- Biotechnology & Pharmaceuticals46
- Consulting & Professional Services5
- Distribution & Wholesale4
- Medical Devices3
- Science & Research3
Senior Level Regulatory Affairs Project Manager Jobs: Frequently Asked Questions
How do I get a senior level regulatory affairs project manager job?
Employers hiring at this level look for candidates who have owned regulatory submissions end-to-end, managed relationships with agencies like the FDA or EMA, and led cross-functional teams through complex approval cycles. Demonstrating that you have set regulatory strategy, not just executed it, and that you have mentored junior staff or coordinated multi-site programs gives your application a clear edge over mid-level candidates.
Which companies hire senior level regulatory affairs project managers?
Companies hiring senior level regulatory affairs project managers right now include Revolution Medicines, Revolution Medicines, and Insmed Incorporated, based on current listings on Migrate Mate as of November 2026. Hiring at this level is concentrated among pharmaceutical manufacturers, medical device companies, biotechnology firms, and contract research organizations that manage large regulatory portfolios across multiple product lines.
Are there remote senior level regulatory affairs project manager jobs?
Yes, though availability varies by employer and product type. About 34% of senior level regulatory affairs project manager openings are remote or hybrid as of November 2026, reflecting broader industry flexibility for experienced professionals who can manage agency interactions and cross-functional teams without being on-site every day.
What makes a regulatory affairs project manager role senior level?
Senior level roles are defined by ownership and scope. Where mid-level positions execute within defined processes, senior roles require setting regulatory strategy, resolving ambiguous agency feedback, and driving timelines across multiple programs simultaneously. They also typically involve mentoring junior team members, influencing senior stakeholders, and making risk-based decisions that affect product development or market access.
Which industries hire the most senior level regulatory affairs project managers?
Senior Level regulatory affairs project manager roles concentrate in Biotechnology & Pharmaceuticals, Consulting & Professional Services, and Distribution & Wholesale, based on current listings on Migrate Mate as of November 2026. These sectors drive demand because they operate under strict regulatory oversight, maintain large submission portfolios, and require experienced professionals who can manage complex, multi-jurisdiction approval processes.