Regulatory Affairs Analyst Jobs in New Jersey
Regulatory Affairs Analyst jobs in New Jersey are concentrated in the pharmaceutical and medical device corridors of central and northern New Jersey, particularly around Princeton, Parsippany, and the Raritan Valley, where employers like Johnson & Johnson, Novartis, and Becton Dickinson maintain major operations. The most in-demand specialties are pharmaceutical submissions and labeling compliance, medical device quality systems, and FDA regulatory strategy. Demand runs from entry-level specialists supporting submission teams to senior analysts leading IND and NDA filings. See the openings below and apply to the ones that match your experience.
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Showing 5 of 56+ Regulatory Affairs Analyst 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 Analyst Jobs in New Jersey
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Find JobsRegulatory Affairs Analyst Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Regulatory Affairs Analyst 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 analyst jobs across New Jersey.
- Bachelor's degree in life sciences, pharmacy, chemistry, or a related scientific field
- Experience preparing and submitting regulatory documents to FDA, including INDs or NDAs
- Familiarity with FDA regulations for pharmaceuticals, biologics, or medical devices
- Proficiency with electronic submission tools such as eCTD publishing software
- Knowledge of ICH guidelines and Good Manufacturing Practice or Good Clinical Practice standards
- Strong technical writing skills for preparing regulatory correspondence and submission summaries
Regulatory Affairs Analyst Jobs in New Jersey: Frequently Asked Questions
How do you become a regulatory affairs analyst in New Jersey?
Most regulatory affairs analyst positions in New Jersey require a bachelor's degree in a life science such as biology, chemistry, or pharmacy, though many employers in the state's dense pharmaceutical corridor prefer candidates with a master's or RAC certification from the Regulatory Affairs Professionals Society. There is no state-issued license specific to regulatory affairs work in New Jersey, but RAC certification is widely recognized by New Jersey employers as a meaningful credential that sets candidates apart.
Which companies hire regulatory affairs analysts in New Jersey?
New Jersey regulatory affairs analyst roles are posted by Merck, Insmed Incorporated, and BD and others right now, based on current listings on Migrate Mate as of September 2026. New Jersey's dense concentration of pharmaceutical and medical device headquarters makes it one of the most active states in the country for this role.
Which New Jersey cities have the most regulatory affairs analyst jobs?
Morristown, New Jersey, and Rahway have the most regulatory affairs analyst openings in New Jersey. The distribution reflects the state's pharmaceutical and biotech industry clusters, with central New Jersey's Raritan Valley and Princeton area anchored by major drug company campuses, while northern New Jersey cities benefit from proximity to large corporate headquarters and contract research organizations.
Are there remote regulatory affairs analyst jobs in New Jersey?
Yes, and more than most scientific roles, since regulatory affairs work is documentation- and review-focused rather than lab-based. About 71% of regulatory affairs analyst openings tied to New Jersey are remote or hybrid as of September 2026, reflecting how well document preparation, submission coordination, and agency correspondence translate to off-site work. Roles involving on-site audits or manufacturing site support are more likely to require in-person presence.
How can I get hired as a regulatory affairs analyst in New Jersey with little or no experience?
The most realistic entry path is through a regulatory affairs associate or regulatory coordinator role at a New Jersey contract research organization or mid-size pharmaceutical company, where the scope is narrower and on-the-job training is common. Large employers like Johnson & Johnson and Novartis also run rotational development programs that include regulatory functions. Candidates coming from adjacent roles such as quality assurance specialist, clinical data coordinator, or scientific writer have a strong basis for the lateral move, and pursuing RAC certification while applying strengthens a profile considerably.
Where can I find and apply to regulatory affairs analyst jobs in New Jersey?
You can find and apply to regulatory affairs analyst jobs in New Jersey on Migrate Mate, which lists current openings in the state. Search the listings to find roles that match your experience level and specialty area, then apply directly to the ones that fit.
See All 56 Regulatory Affairs Analyst Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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