Regulatory Affairs Associate Jobs
Regulatory Affairs Associate jobs are open across pharmaceuticals, medical devices, biotechnology, and consumer products, from entry-level to senior associate roles, with specializations in FDA submissions, labeling compliance, and clinical trial documentation. Find a role that fits from the openings below and apply directly.
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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
Regulatory Affairs Associate Jobs by Experience Level
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Find JobsRegulatory Affairs Associate Job Market
Who's Hiring
- Katalyst Healthcares & Life Sciences48

- Revolution Medicines18

- AbbVie17

- BD13

- Abbott11

Top Industries Hiring
- Biotechnology & Pharmaceuticals59
- Medical Devices11
- Healthcare & Medical Services10
- Consulting & Professional Services9
- Science & Research5
What Employers Look For
The qualifications that appear most often in regulatory affairs associate jobs.
- Bachelor's degree in life sciences, chemistry, engineering, or a related scientific field
- Hands-on experience preparing or supporting FDA regulatory submissions such as 510(k), NDA, or BLA
- Working knowledge of FDA regulations including 21 CFR Parts 11, 820, and 210/211
- Proficiency with regulatory information management systems and electronic document control software
- Strong technical writing skills demonstrated through SOPs, labeling documents, or regulatory summaries
- Regulatory Affairs Certification (RAC) from RAPS or active candidacy preferred by many employers
Tips for Your Regulatory Affairs Associate Job Search
Tailor your resume to submission types
List the specific submission types you've worked on, such as 510(k), PMA, NDA, or BLA, rather than just naming the agency. Hiring managers scan for exact acronyms, and a generic 'regulatory submissions' line won't pass an ATS filter targeting those terms.
Get your RAC credential before applying
The Regulatory Affairs Certification from RAPS signals baseline competency to screeners who don't have a regulatory background themselves. Candidates with RAC credentials move faster through initial screening at mid-size and large medical device companies, so time your applications accordingly.
Apply early to roles that fit
Migrate Mate lists regulatory affairs associate openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Target postings by product classification
Search for openings by Class II or Class III device, OTC drug, or biologics, not just by job title. Companies organized by product type want associates who already know the relevant regulatory pathway, so matching your background to the product class dramatically improves your callback rate.
Prepare case answers for real submissions
Interviewers at regulated companies almost always ask you to walk through a submission you managed, including the agency feedback you received. Have a concise narrative ready for at least one complete regulatory cycle, from initial strategy through approval or clearance, with specific obstacles you resolved.
Negotiate using scope, not just base pay
In regulatory affairs, the range of products you're assigned and the chance to lead submissions solo matter as much as salary for long-term career growth. When you get an offer, ask directly which product lines you'd own and whether you'd handle agency correspondence independently from day one.
Regulatory Affairs Associate Jobs: Frequently Asked Questions
Which companies are hiring the most regulatory affairs associates?
The companies hiring the most regulatory affairs associates right now include Katalyst Healthcares & Life Sciences, Revolution Medicines, and AbbVie, with the largest share of openings in California, Massachusetts, and New Jersey, based on current listings on Migrate Mate as of November 2026. Pharmaceutical manufacturers, contract research organizations, and medical device firms consistently post the highest volumes of associate-level regulatory openings.
How many regulatory affairs associate jobs are remote?
About 72% of regulatory affairs associate openings are fully remote or hybrid as of November 2026, making it one of the more flexible roles in the life sciences field. Submission coordination and regulatory writing roles tend to have the highest remote availability, while positions involving lab access, device testing oversight, or in-person agency meetings are more often on-site.
How do you become a regulatory affairs associate?
Start with a bachelor's degree in a life science, chemistry, or engineering discipline, then gain exposure to regulated environments through internships, quality assurance roles, or clinical operations positions. Build familiarity with FDA guidance documents and the Code of Federal Regulations relevant to your target product type. Pursuing the RAC credential through RAPS strengthens your application significantly, and entry-level openings at contract research organizations are often the most accessible first step into the field.
Can I get a regulatory affairs associate job with little experience?
Yes, candidates with limited direct regulatory experience can break in by highlighting adjacent work in quality assurance, clinical trial coordination, or laboratory compliance. Demonstrating that you've read and applied FDA guidance documents, written SOPs, or supported an audit shows practical readiness even without a formal regulatory title. Targeting smaller companies or contract research organizations with high submission volumes gives you the fastest path to hands-on experience.
What does the regulatory affairs associate interview process look like?
Most regulatory affairs associate interviews follow a structured process that begins with a recruiter screen focused on your regulatory background and product experience, followed by a technical interview with the hiring manager covering specific submission types and relevant regulations. Many companies include a writing exercise or case study asking you to review a mock submission or draft a response to agency feedback. A final panel interview with cross-functional colleagues in quality, clinical, or R&D is common before an offer is extended.
Where can I find and apply to regulatory affairs associate jobs?
You can find and apply to regulatory affairs associate jobs on Migrate Mate, which lists current openings from across the United States. Find roles that match your background and apply directly to each listing without leaving the platform.
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