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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Role Overview:
The Associate Director is responsible for the review and approval of all US promotional materials and serving as the promotional regulatory expert with legal, medical and commercial colleagues to ensure that promotional practices are consistent with regulatory guidelines, our Company's policies, and support business objectives.
- Serve as the liaison and manage correspondence with FDA’s promotional review divisions OPDP/APLB, including complex regulatory questions and submissions for advisory comment.
- Propose creative, effective, and compliant regulatory strategies and solutions to challenging promotional concepts that meet business objectives and minimize regulatory risk.
- Provide regulatory consultation in the development and implementation of US marketing strategy and promotional programs.
- Support the US commercial teams, including relevant stakeholders, by participating in strategy discussions and extended team meetings and providing regulatory guidance and perspective on marketing strategies and promotion objectives and tactics. Provide promotional regulatory input on concepts and draft materials to help ensure promotional materials are aligned with U.S. promotional regulations, corporate standards and policies and business objectives.
- Actively participate in labeling and global regulatory team meetings to ensure support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the use of study results in U.S. promotion.
- Maintain current awareness and understanding of FDA advisory correspondence, evolving FDA regulations and guidance documents, FDA enforcement letters and policy issues affecting the pharmaceutical/biologics industry and clearly articulate regulatory rationale.
- Ability to take on more complex projects and provide promotional regulatory training and coaching to team members.
- Contribute to the development of departmental strategic initiatives to drive effective, compliant promotional regulatory review.
Qualifications, Skills & Experience:
Minimum Requirement:
- B.A. or B.S. degree with an emphasis in science, health care or related fields.
- Master’s, PhD or PharmD degree with an emphasis in science, health care or related fields
- Minimum of five years of pharmaceutical/biologics industry or related experience with an emphasis in regulatory or scientific disciplines
- Minimum of two years of direct experience as the primary regulatory reviewer of advertising and promotional materials
- Demonstrated knowledge of FDA regulations relating to advertising and promotion for prescription products
- Proactive with strong cross-functional collaboration skills
- Demonstrated history of successful interactions with the promotional review divisions of FDA (OPDP/APLB) or experience developing/leading the regulatory strategy for a product filing/launch
- Understanding of the product development and labeling process
- Excellent verbal and written communication skills
- Attention to detail and ability to manage multiple priorities simultaneously.
- Strong interpersonal skills with ability to demonstrate strategic and analytical thinking
- Demonstrated ability to negotiate and influence others effectively
#EligibleforERP
Required Skills:
Clinical Trials, Cross-Functional Teamwork, Data Analysis, Detail-Oriented, Electronic Common Technical Document (eCTD), FDA Regulations, Negotiation, Pharmaceutical Industry, Promotional Review, Regulatory Compliance, Regulatory Strategies, Regulatory Submissions, Stakeholder Management, Strategic Thinking, US Regulatory Affairs
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement​
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
The primary location for this posting is:
USA - Pennsylvania - North Wales (Upper Gwynedd)
Where required by law, the compensation range for this role is provided below.
The salary range for the primary location of this role is:
$129,000.00 - $203,100.00
This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.
Additional location(s) Compensation Information:
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
11/21/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Requisition ID: R424596
See All 70 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
- Education
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 Insmed Incorporated, BD, and AbbVie and others right now, based on current listings on Migrate Mate as of November 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?
Bridgewater, Florham Park, and Franklin Lakes 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 73% of regulatory affairs analyst openings tied to New Jersey are remote or hybrid as of November 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 70 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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