Regulatory Compliance Specialist Jobs in New Jersey
Regulatory Compliance Specialist jobs in New Jersey are open across Princeton, Bridgewater, and Mahwah and other New Jersey metros, with employers like Artech, ImmunityBio, and Integra LifeSciences hiring at every experience level. Find a role that fits below and apply directly.
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See related jobsWhy 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 5 Regulatory Compliance Specialist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find JobsRegulatory Compliance Specialist Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Regulatory Compliance Specialist Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
- Artech1
- ImmunityBio1
- Integra LifeSciences1
- Stryker1
- Taiho Oncology1
Top Industries Hiring
- Biotechnology & Pharmaceuticals2
- Medical Devices2
- Consulting & Professional Services1
What New Jersey Employers Look For
The qualifications that appear most often in regulatory compliance specialist jobs across New Jersey.
- Bachelor's degree in business, law, finance, or a related field
- Knowledge of relevant regulatory frameworks such as SOX, HIPAA, FDA, or EPA standards
- Experience conducting internal audits or compliance assessments
- Proficiency with compliance management software or GRC platforms
- Strong written communication skills for policy documentation and regulatory reporting
- Professional certification such as CCEP, CRCM, or CHC preferred
Regulatory Compliance Specialist Jobs in New Jersey: Frequently Asked Questions
How many regulatory compliance specialist jobs are there in New Jersey?
There are 5+ regulatory compliance specialist openings in New Jersey on Migrate Mate as of June 2026, with the most roles in Princeton, Bridgewater, and Mahwah. New positions post regularly as employers across New Jersey hire.
How much do regulatory compliance specialists make in New Jersey?
Regulatory compliance specialists 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 compliance specialist jobs?
Princeton, Bridgewater, and Mahwah have the most regulatory compliance specialist openings in New Jersey right now, with additional roles spread across smaller metros statewide.
Which companies hire regulatory compliance specialists in New Jersey?
Employers hiring regulatory compliance specialists in New Jersey include Artech, ImmunityBio, and Integra LifeSciences, based on current listings on Migrate Mate as of June 2026.
Are there remote regulatory compliance specialist jobs in New Jersey?
Yes. About 20% of regulatory compliance specialist 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 compliance specialist jobs in New Jersey?
You can apply to regulatory compliance specialist 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 5 Regulatory Compliance Specialist Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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