Regulatory Affairs Manager Jobs in New Jersey
Regulatory Affairs Manager jobs in New Jersey sit at the center of one of the most active markets in the country, driven by the state's dense concentration of pharmaceutical, biotechnology, and medical device companies from the Princeton Corridor through the Meadowlands to the Jersey Shore life sciences cluster. Hiring is strongest in Newark, Parsippany, and Princeton, where established employers like Johnson & Johnson, Merck, and Becton Dickinson maintain major operations. Demand runs from associate-level regulatory coordinators entering the field through senior managers overseeing global submissions. Find a role that fits below and apply directly.
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Showing 5 of 56+ Regulatory Affairs Manager jobs
Job title: Senior Manager, Regulatory Affairs Advertising and Promotion
Location: Morristown, NJ/Cambridge, MA
About the job
As the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. Ready to get started?
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.
With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches. As the product A&P expert, contribute to the development and implementation of regulatory strategies for labeling, product defense, and development projects. Serve as the primary liaison with FDA, for assigned products, on matters related to advertising and promotional compliance matters.
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
Identifies product-specific or therapeutic area A&P issues and works with other teams to propose and implement solutions.
Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.
Oversees and bears responsibility for the successful implementation of regulatory strategic objectives and projects with minimal supervision.
Active participant and Regulatory representative on brand teams and Review Committees (RC) for commercial and medical materials, respectively.
Provides guidance and feedback to internal Sanofi constituencies (commercial groups, R&D) to maximize the competitive impact of product development as well as ultimate promotion, advertising, and reimbursement. Provides input to the Global organization on domestic regulatory strategies for in-line products through life cycle management programs.
Contribute A&P expertise to the development of optimal labeling on new and supplemental new drug applications.
Provides product-specific Regulatory strategies to mitigate risk; works in conjunction with brand team management to provide advice and risk/benefit analysis to maximize value to stakeholders.
Performs other duties as assigned.
About You
Basic Qualifications:
Bachelor’s degree from an accredited four-year college or university; Science focus preferred, but not require
Work Experience Required:
3+ Years experience within pharmaceutical or medical device advertising and promotional review.
Successful track record with relevant regulatory experience.
Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc.
Knowledge, Skills and Equivalent Experience:
Knowledge and understanding of complex medical and scientific subject matter.
Ability to work well within cross-functional teams.
Demonstrates solid oral communication and writing skills.
Understanding of the U.S. pharmaceutical marketplace, and familiarity with medical terminology.
Understands issues, problems and opportunities by comparing data from different sources to draw conclusions and then can choose a course of action or develop the appropriate solution.
Develops collaborative relationships to facilitate the accomplishment of work goals.
Develops and proposes innovative solutions in work situations, trying different and novel ways to deal with work problems and opportunities.
Shows ability to use appropriate interpersonal styles and techniques to gain acceptance of ideas or plans.
Can build collaborative internal networks to obtain cooperation.
Unquestionable ethics, professional integrity and personal values consistent with the Sanofi values.
Is able to balance projects with day-to-day duties, ensuring participation from other members of the department as needed.
Is able to establish priorities and timelines to effectively manage workload. Is able to multi-task well.
Deals with people in an honest and forthright manner representing information and data accurately.
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Help improve the lives of millions of people globally by making drug development quicker and more effective.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA #LI-SA
#LI-Hybrid
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Job title: Senior Manager, Regulatory Affairs Advertising and Promotion
Location: Morristown, NJ/Cambridge, MA
About the job
As the Senior Manager, Regulatory Affairs Advertising and Promotion within our GRA Advertising and Promo Team, you will be responsible for conducting the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns. Ready to get started?
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.
With some direction from the Therapeutic Area Head, will conduct the independent review of advertising, promotional, communications and other materials, and help develop and implement regulatory strategies for promotion and advertising campaigns, including serving as regulatory lead for product launches. As the product A&P expert, contribute to the development and implementation of regulatory strategies for labeling, product defense, and development projects. Serve as the primary liaison with FDA, for assigned products, on matters related to advertising and promotional compliance matters.
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
Identifies product-specific or therapeutic area A&P issues and works with other teams to propose and implement solutions.
Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.
Oversees and bears responsibility for the successful implementation of regulatory strategic objectives and projects with minimal supervision.
Active participant and Regulatory representative on brand teams and Review Committees (RC) for commercial and medical materials, respectively.
Provides guidance and feedback to internal Sanofi constituencies (commercial groups, R&D) to maximize the competitive impact of product development as well as ultimate promotion, advertising, and reimbursement. Provides input to the Global organization on domestic regulatory strategies for in-line products through life cycle management programs.
Contribute A&P expertise to the development of optimal labeling on new and supplemental new drug applications.
Provides product-specific Regulatory strategies to mitigate risk; works in conjunction with brand team management to provide advice and risk/benefit analysis to maximize value to stakeholders.
Performs other duties as assigned.
About You
Basic Qualifications:
Bachelor’s degree from an accredited four-year college or university; Science focus preferred, but not require
Work Experience Required:
3+ Years experience within pharmaceutical or medical device advertising and promotional review.
Successful track record with relevant regulatory experience.
Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc.
Knowledge, Skills and Equivalent Experience:
Knowledge and understanding of complex medical and scientific subject matter.
Ability to work well within cross-functional teams.
Demonstrates solid oral communication and writing skills.
Understanding of the U.S. pharmaceutical marketplace, and familiarity with medical terminology.
Understands issues, problems and opportunities by comparing data from different sources to draw conclusions and then can choose a course of action or develop the appropriate solution.
Develops collaborative relationships to facilitate the accomplishment of work goals.
Develops and proposes innovative solutions in work situations, trying different and novel ways to deal with work problems and opportunities.
Shows ability to use appropriate interpersonal styles and techniques to gain acceptance of ideas or plans.
Can build collaborative internal networks to obtain cooperation.
Unquestionable ethics, professional integrity and personal values consistent with the Sanofi values.
Is able to balance projects with day-to-day duties, ensuring participation from other members of the department as needed.
Is able to establish priorities and timelines to effectively manage workload. Is able to multi-task well.
Deals with people in an honest and forthright manner representing information and data accurately.
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
Help improve the lives of millions of people globally by making drug development quicker and more effective.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA #LI-SA
#LI-Hybrid
#vhd
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
See All 56 Regulatory Affairs Manager Jobs in New Jersey
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Find JobsRegulatory Affairs Manager Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Regulatory Affairs Manager Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Healthcare & Medical Services
What New Jersey Employers Look For
The qualifications that appear most often in regulatory affairs manager jobs across New Jersey.
- Bachelor's degree in life sciences, pharmacy, chemistry, or a related scientific field
- Three or more years of regulatory affairs experience in pharmaceutical or medical device industry
- Working knowledge of FDA submission processes including INDs, NDAs, BLAs, or 510(k)s
- RAC certification from the Regulatory Affairs Professionals Society preferred or required
- Experience with eCTD document management systems and electronic submission platforms
- Strong written communication skills for authoring regulatory documents and agency correspondence
Regulatory Affairs Manager Jobs in New Jersey: Frequently Asked Questions
How do you become a regulatory affairs manager in New Jersey?
Most regulatory affairs managers in New Jersey enter through a bachelor's degree in pharmacy, biology, chemistry, or engineering, then build experience in quality assurance or clinical operations at one of the state's many pharmaceutical or device companies. New Jersey does not require a state-issued license specific to this role, but the Regulatory Affairs Professionals Society's RAC credential is widely expected by New Jersey employers and strengthens candidacy for senior positions.
How much do regulatory affairs managers make in New Jersey?
Regulatory affairs managers in New Jersey earn a median of about $100,000 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $58,860 for the lowest 10% to over $158,540 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire regulatory affairs managers in New Jersey?
Employers hiring regulatory affairs managers in New Jersey right now include Merck, Insmed Incorporated, and BD, based on current listings on Migrate Mate as of September 2026. New Jersey's life sciences corridor, which runs through Morris, Somerset, and Middlesex counties, means the majority of these openings sit within large pharmaceutical headquarters or their contract research and manufacturing partners.
Which New Jersey cities have the most regulatory affairs manager jobs?
Morristown, New Jersey, and Rahway have the most regulatory affairs manager openings in New Jersey. The distribution reflects the state's pharmaceutical and biotech anchors: Parsippany and Princeton are home to global drug company headquarters and regional offices, while Newark draws openings tied to hospital systems and the growing life sciences presence near its airport corridor.
Are there remote regulatory affairs manager jobs in New Jersey?
Yes, and more than most fields. Regulatory affairs is largely document-driven and submission-focused, making it well suited to remote work. About 71% of regulatory affairs manager openings tied to New Jersey are remote or hybrid as of September 2026, reflecting how widely New Jersey pharmaceutical employers have adopted flexible arrangements since the pandemic. Submissions management, labeling review, and agency correspondence are the functions most commonly done fully remote.
How can I get hired as a regulatory affairs manager in New Jersey with little or no experience?
The most realistic entry path is through a regulatory affairs associate or coordinator role at a New Jersey contract research organization or mid-size pharmaceutical company, where responsibilities include dossier formatting, archiving, and tracking agency correspondence. Johnson & Johnson, Merck, and Becton Dickinson all run new-graduate rotational programs that include regulatory functions. Candidates moving laterally from quality assurance, clinical data management, or pharmacovigilance roles have a strong foundation, and completing a RAC examination prep course signals seriousness to hiring managers.
Where can I find and apply to regulatory affairs manager jobs in New Jersey?
You can find and apply to regulatory affairs manager jobs in New Jersey on Migrate Mate, which lists current openings across the state's pharmaceutical, biotech, and medical device sectors. Search the available roles, find the ones that match your background and location preference, and apply directly.
See All 56 Regulatory Affairs Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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