Entry Level Regulatory Affairs Manager Jobs
New grad regulatory affairs manager jobs connect recent graduates and entry level candidates with zero to two years of experience to a field where internship work or a strong portfolio of coursework and submissions can matter more than a long resume. Most openings include on-site, remote, and hybrid positions across Biotechnology & Pharmaceuticals, Insurance, and Distribution & Wholesale, with employers like Oscar Health, Abbott, and Laborie hiring at this level now.
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INTRODUCTION
We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact on the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
ROLE AND RESPONSIBILITIES
Laborie Medical Technologies is currently searching for a Regulatory Affairs Specialist to join our team in hybrid role based out of the Portsmouth, NH or Minnetonka, MN offices. The Regulatory Affairs Specialist will support global product registration, approval, and lifecycle maintenance activities across key markets, including the United States, Canada, Europe, and other international regions. This role is responsible for ensuring that regulatory approvals are obtained, maintained, and renewed in accordance with applicable regulatory requirements and internal standards. The individual will contribute to regulatory strategy and execution for assigned product lines, including preparing and submitting regulatory submissions, managing product registrations and renewals, and ensuring ongoing compliance with global regulatory requirements. The Regulatory Affairs Specialist will work cross-functionally to support product changes, maintain regulatory documentation, and ensure alignment with established corporate procedures and quality standards.
About the Role:
Preparing and submitting documentation necessary for regulatory approval of assigned products.
Defining worldwide regulatory requirements necessary for regulatory approval of assigned products, and advising cross-functional teams on regulatory strategies.
Executing product submission strategies as directed.
Maintaining all regulatory documentation to ensure availability for external audits and preparation of submission packages.
Maintaining a thorough knowledge of current regulatory requirements.
Executing on additional responsibilities as defined by management.
MINIMUM QUALIFICATIONS
Bachelor’s degree in Science, Engineering, or other relevant discipline
1-3 years' experience in Regulatory Affairs in the medical device industry
1-3 years' experience in international registrations
Working knowledge of quality system regulations and guidelines
Great communication skills with all levels of personnel
High level of organization and planning skills
* Working knowledge of medical devices, procedures, and terminology
WHY LABORIE
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
Paid time off and paid volunteer time
Medical, Dental, Vision and Flexible Spending Account
Health Savings Account with Company Funded Contributions
401k Retirement Plan with Company Match
Parental Leave and Adoption Services
Health and Wellness Programs and Events
* Awarded 2025 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.
INTRODUCTION
We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact on the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.
ROLE AND RESPONSIBILITIES
Laborie Medical Technologies is currently searching for a Regulatory Affairs Specialist to join our team in hybrid role based out of the Portsmouth, NH or Minnetonka, MN offices. The Regulatory Affairs Specialist will support global product registration, approval, and lifecycle maintenance activities across key markets, including the United States, Canada, Europe, and other international regions. This role is responsible for ensuring that regulatory approvals are obtained, maintained, and renewed in accordance with applicable regulatory requirements and internal standards. The individual will contribute to regulatory strategy and execution for assigned product lines, including preparing and submitting regulatory submissions, managing product registrations and renewals, and ensuring ongoing compliance with global regulatory requirements. The Regulatory Affairs Specialist will work cross-functionally to support product changes, maintain regulatory documentation, and ensure alignment with established corporate procedures and quality standards.
About the Role:
Preparing and submitting documentation necessary for regulatory approval of assigned products.
Defining worldwide regulatory requirements necessary for regulatory approval of assigned products, and advising cross-functional teams on regulatory strategies.
Executing product submission strategies as directed.
Maintaining all regulatory documentation to ensure availability for external audits and preparation of submission packages.
Maintaining a thorough knowledge of current regulatory requirements.
Executing on additional responsibilities as defined by management.
MINIMUM QUALIFICATIONS
Bachelor’s degree in Science, Engineering, or other relevant discipline
1-3 years' experience in Regulatory Affairs in the medical device industry
1-3 years' experience in international registrations
Working knowledge of quality system regulations and guidelines
Great communication skills with all levels of personnel
High level of organization and planning skills
* Working knowledge of medical devices, procedures, and terminology
WHY LABORIE
Our Mission every day is to operate as a world-class specialist medical company making and advancing technologies that preserve and restore human dignity. We do that today by helping people with pelvic and gastrointestinal conditions live normal lives, and by helping mothers and babies have safe deliveries.
Paid time off and paid volunteer time
Medical, Dental, Vision and Flexible Spending Account
Health Savings Account with Company Funded Contributions
401k Retirement Plan with Company Match
Parental Leave and Adoption Services
Health and Wellness Programs and Events
* Awarded 2025 Cigna Healthy Workforce Designation Gold Level
Laborie provides equal employment opportunities and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Laborie is committed to providing access and reasonable accommodation in our services, activities, education, and employment for individuals with disabilities.
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Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals10
- Insurance5
- Distribution & Wholesale3
- Healthcare & Medical Services3
- Education2
Entry Level Regulatory Affairs Manager Jobs: Frequently Asked Questions
How do I get an entry level regulatory affairs manager job?
Focus on demonstrating familiarity with regulatory frameworks, submission processes, and documentation standards even if your experience comes from internships, coursework, or cooperative education programs. Employers at this level look for candidates who understand compliance workflows and can organize complex information carefully. A science or health-related degree, exposure to FDA or similar agency processes, and any hands-on lab or regulatory project work all strengthen your application meaningfully.
Which companies hire entry level regulatory affairs managers?
Companies hiring entry level regulatory affairs managers right now include Oscar Health, Abbott, and Laborie, based on current listings on Migrate Mate as of August 2026. At this level, hiring comes from pharmaceutical manufacturers, medical device companies, biotechnology firms, and contract research organizations that build junior regulatory teams to support submission pipelines and compliance programs.
Are there remote entry level regulatory affairs manager jobs?
Yes, though on-site roles remain common at this stage. About 38% of entry level regulatory affairs manager openings are remote or hybrid as of August 2026, reflecting broader flexibility in the industry. Remote positions often require strong self-direction and familiarity with digital submission platforms, since you may be working with cross-functional teams and regulatory databases without in-person guidance.
Are these new grad regulatory affairs manager jobs?
Yes, many of these listings are new grad and junior roles that welcome recent graduates with little or no professional experience. A new grad friendly posting typically signals this by welcoming zero to two years of experience, accepting internship or co-op work in lieu of full-time history, or specifying that a relevant degree or regulatory coursework is the primary qualification. Junior titles are common at this level too.
Which industries hire the most entry level regulatory affairs managers?
Entry Level regulatory affairs manager roles concentrate in Biotechnology & Pharmaceuticals, Insurance, and Distribution & Wholesale, based on current listings on Migrate Mate as of August 2026. These sectors drive the most entry level hiring because they operate under strict product approval and compliance requirements, creating ongoing demand for junior professionals who can support documentation, submissions, and regulatory strategy under experienced team leadership.