Regulatory Affairs Jobs in New Jersey
Regulatory affairs jobs in New Jersey are among the most active in the country, concentrated in pharmaceutical, biotech, and medical device companies that have long made the state their home. Hiring runs from entry-level regulatory coordinators through senior directors and vice presidents, with the heaviest demand in Princeton, Parsippany, and the Route 1 corridor. Johnson and Johnson, Merck, and Becton Dickinson are among the established employers with deep roots in New Jersey that consistently recruit for regulatory affairs talent. The most sought-after specialties are drug submissions, FDA compliance, and quality systems. Find a role that fits below and apply directly.
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Showing 5 of 56+ Regulatory Affairs 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 Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Regulatory Affairs JobsRegulatory Affairs Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Regulatory Affairs 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 jobs across New Jersey.
- Bachelor's degree in a life sciences, chemistry, or engineering discipline required
- Experience with FDA regulatory submissions including INDs, NDAs, or 510(k)s
- Familiarity with ICH guidelines, 21 CFR regulations, and GxP standards
- Proficiency with regulatory information management systems such as Veeva Vault
- Strong technical writing skills for preparing regulatory documents and dossiers
- RAC certification from the Regulatory Affairs Professionals Society preferred by many employers
Regulatory Affairs Jobs in New Jersey: Frequently Asked Questions
How do you become a regulatory affairs professional in New Jersey?
Most regulatory affairs roles in New Jersey require a bachelor's degree in a life sciences field such as biology, chemistry, pharmacology, or biomedical engineering, and many employers prefer candidates with a master's degree. New Jersey does not issue a state license for regulatory affairs specifically, but employers consistently value the Regulatory Affairs Certification from the Regulatory Affairs Professionals Society. Candidates who build experience in quality assurance, clinical operations, or laboratory research at New Jersey's many pharmaceutical and biotech companies often transition into regulatory roles from those adjacent positions.
How much do regulatory affairses make in New Jersey?
Regulatory affairses 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 professionals in New Jersey?
Employers hiring regulatory affairs professionals 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 dense concentration of major pharmaceutical headquarters and biotech campuses means openings appear consistently throughout the year, particularly along the Route 1 and Route 202 corridors where many global life sciences companies maintain their regulatory functions.
Which New Jersey cities have the most regulatory affairs jobs?
The cities with the most regulatory affairs openings in New Jersey are Morristown, New Jersey, and Rahway. The distribution reflects the state's pharmaceutical and biotech geography, with Princeton and its surrounding townships anchoring a cluster of global drug company headquarters, while Parsippany and Bridgewater attract medical device and specialty pharma employers whose regulatory teams are based on-site at their New Jersey campuses.
Are there remote regulatory affairs jobs in New Jersey?
Yes, and more than most fields. About 71% of regulatory affairs openings tied to New Jersey are remote or hybrid as of September 2026, reflecting the desk-based and document-driven nature of much of the work. Submission writing, regulatory strategy, and labeling review tend to be the functions most frequently offered with remote or hybrid flexibility, while roles that require direct interaction with manufacturing or laboratory operations are more likely to be on-site.
How can I get hired as a regulatory affairs professional in New Jersey with little or no experience?
The most realistic entry path is a quality assurance associate or clinical research coordinator role at one of New Jersey's large pharmaceutical or contract research organizations, which regularly hire recent graduates and provide exposure to regulatory workflows. Companies such as Merck, Johnson and Johnson, and Becton Dickinson run rotational or early-career programs that include regulatory affairs rotations. Completing a RAC certification exam and building a portfolio of regulatory writing samples, even from academic or volunteer projects, gives candidates a meaningful edge when competing for junior regulatory specialist openings.
Where can I find and apply to regulatory affairs jobs in New Jersey?
You can find and apply to regulatory affairs jobs in New Jersey on Migrate Mate, which lists current openings from employers actively hiring in the state. Find roles that fit your experience and specialization and apply directly to the ones that match.
See All 56 Regulatory Affairs Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Regulatory Affairs Jobs