Regulatory Affairs Jobs in New Jersey
Regulatory Affairs jobs in New Jersey are open across Florham Park, Princeton, and Basking Ridge and other New Jersey metros, with employers like AbbVie, Insmed Incorporated, and Artech hiring at every experience level. Find a role that fits below and apply directly.
Find Regulatory Affairs JobsOverview
Showing 5 of 23+ Regulatory Affairs jobs
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits.
Stryker is hiring a Staff Regulatory Affairs Specialist in Mahwah, NJ to support new product development for our Joint Replacement implant and instrument portfolio across U.S and international markets. This role focuses on developing regulatory strategies, guiding product development teams, and preparing submissions to achieve market access across U.S. and international markets.
What you will do
- Assess regulatory intelligence and update local, regional, and global regulatory strategies based on evolving requirements
- Evaluate the regulatory environment and provide guidance across product lifecycle phases including development, manufacturing, and commercialization
- Determine product classification, submission requirements, and approval pathways across domestic and international markets
- Prepare and submit regulatory filings in accordance with applicable global regulations and timelines
- Identify regulatory risks and obstacles, propose mitigation strategies, and recommend refinements based on regulatory outcomes
- Provide regulatory guidance on quality, preclinical, and clinical documentation to ensure submission readiness and compliance
- Communicate with regulatory authorities to support submissions, monitor review progress, and respond to agency requests
- Develop or update regulatory procedures and train cross-functional stakeholders to maintain compliance across the organization
What you will need
Required Qualifications
- Bachelor’s degree required. Preferred to be in Engineering, Science, or a related field
- Minimum 4 years of experience in regulatory affairs within a regulated industry
- Experience within the medical device industry
Preferred Qualifications
- Master’s degree in Regulatory Science or related discipline
- Regulatory Affairs Certification (RAC)
- Knowledge of 510(k) and/or CE marking pathways
- Experience preparing and submitting regulatory filings (e.g., FDA, EU, or international submissions)
- Experience supporting product lifecycle regulatory activities (development through post-market)
Posted Date: 06/19/2026
This role will be posted for a minimum of 3 days.
United States of America Pay Ranges:
- Puerto Rico: $77,700 - $129,500 USD Annual
- USN: $95,700 - $159,500 USD Annual
- US5: $100,500 - $167,500 USD Annual
- US10: $105,300 - $175,500 USD Annual
- US15: $110,100 - $183,400 USD Annual
- US20: $114,800 - $191,400 USD Annual
- US30: $124,400 - $207,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
Job description
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more: US Stryker employee benefits.
Stryker is hiring a Staff Regulatory Affairs Specialist in Mahwah, NJ to support new product development for our Joint Replacement implant and instrument portfolio across U.S and international markets. This role focuses on developing regulatory strategies, guiding product development teams, and preparing submissions to achieve market access across U.S. and international markets.
What you will do
- Assess regulatory intelligence and update local, regional, and global regulatory strategies based on evolving requirements
- Evaluate the regulatory environment and provide guidance across product lifecycle phases including development, manufacturing, and commercialization
- Determine product classification, submission requirements, and approval pathways across domestic and international markets
- Prepare and submit regulatory filings in accordance with applicable global regulations and timelines
- Identify regulatory risks and obstacles, propose mitigation strategies, and recommend refinements based on regulatory outcomes
- Provide regulatory guidance on quality, preclinical, and clinical documentation to ensure submission readiness and compliance
- Communicate with regulatory authorities to support submissions, monitor review progress, and respond to agency requests
- Develop or update regulatory procedures and train cross-functional stakeholders to maintain compliance across the organization
What you will need
Required Qualifications
- Bachelor’s degree required. Preferred to be in Engineering, Science, or a related field
- Minimum 4 years of experience in regulatory affairs within a regulated industry
- Experience within the medical device industry
Preferred Qualifications
- Master’s degree in Regulatory Science or related discipline
- Regulatory Affairs Certification (RAC)
- Knowledge of 510(k) and/or CE marking pathways
- Experience preparing and submitting regulatory filings (e.g., FDA, EU, or international submissions)
- Experience supporting product lifecycle regulatory activities (development through post-market)
Posted Date: 06/19/2026
This role will be posted for a minimum of 3 days.
United States of America Pay Ranges:
- Puerto Rico: $77,700 - $129,500 USD Annual
- USN: $95,700 - $159,500 USD Annual
- US5: $100,500 - $167,500 USD Annual
- US10: $105,300 - $175,500 USD Annual
- US15: $110,100 - $183,400 USD Annual
- US20: $114,800 - $191,400 USD Annual
- US30: $124,400 - $207,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
See All 23 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
- AbbVie3
- Insmed Incorporated3
- Artech2
- Daiichi Sankyo2
- Haleon2
Top Industries Hiring
- Biotechnology & Pharmaceuticals16
- Consulting & Professional Services2
- Medical Devices2
- Science & Research1
What New Jersey Employers Look For
The qualifications that appear most often in regulatory affairs jobs across New Jersey.
- Bachelor's degree in life sciences, pharmacy, chemistry, or a related field
- Experience with FDA submissions including INDs, NDAs, BLAs, or 510(k)s
- Knowledge of 21 CFR regulations and ICH guidelines
- Proficiency with regulatory information management systems such as Veeva Vault
- Regulatory Affairs Certification (RAC) from RAPS preferred or required
- Strong technical writing skills for regulatory documents and agency correspondence
Regulatory Affairs Jobs in New Jersey: Frequently Asked Questions
How many regulatory affairs jobs are there in New Jersey?
There are 23+ regulatory affairs openings in New Jersey on Migrate Mate as of June 2026, with the most roles in New Jersey, Florham Park, and Princeton. New positions post regularly as employers across New Jersey hire.
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 New Jersey cities have the most regulatory affairs jobs?
New Jersey, Florham Park, and Princeton have the most regulatory affairs openings in New Jersey right now, with additional roles spread across smaller metros statewide.
Which companies hire regulatory affairss in New Jersey?
Employers hiring regulatory affairss in New Jersey include AbbVie, Insmed Incorporated, and Artech, based on current listings on Migrate Mate as of June 2026.
Are there remote regulatory affairs jobs in New Jersey?
Yes. About 39% of regulatory affairs openings tied to New Jersey are remote or hybrid as of June 2026. The rest are on-site roles based in New Jersey metros.
How do I apply for regulatory affairs jobs in New Jersey?
You can apply to regulatory affairs jobs in New Jersey directly on Migrate Mate. Search the listings above, find roles that match your experience and preferred New Jersey location, then apply to each one that fits.
See All 23 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