Entry Level Regulatory Affairs Director Jobs
New grad regulatory affairs director jobs are open to recent graduates and entry level candidates with zero to two years of experience, where strong internship work or a focused academic background in regulatory science can matter more than a long resume. Most openings are on-site roles concentrated in 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 Director Jobs: Frequently Asked Questions
How do I get an entry level regulatory affairs director job?
Employers hiring at this level prioritize candidates with a degree in a life sciences, pharmacy, or engineering field, along with any hands-on exposure to regulatory submissions, quality systems, or compliance processes through coursework, internships, or co-ops. Familiarity with FDA submission formats, knowledge of CFR requirements, and strong technical writing skills give candidates a clear edge when competing for entry level openings.
Which companies hire entry level regulatory affairs directors?
Companies hiring entry level regulatory affairs directors right now include Oscar Health, Abbott, and Laborie, based on current listings on Migrate Mate as of August 2026. Hiring at this level comes primarily from pharmaceutical manufacturers, medical device companies, and biotechnology firms that build regulatory teams through structured entry level pipelines.
Are there remote entry level regulatory affairs director jobs?
Yes, though remote availability at this level is more limited than for senior roles. About 38% of entry level regulatory affairs director openings are remote or hybrid as of August 2026, with the remainder requiring on-site presence for hands-on document review, lab coordination, or team collaboration during the early career stage.
Are these new grad regulatory affairs director jobs?
Yes, these include new grad, recent graduate, and junior regulatory affairs director roles. A posting is new-grad friendly when it welcomes zero to two years of experience, counts internships or co-op rotations toward the requirement, or lists a portfolio of regulatory projects as an acceptable substitute for full-time work history. Many employers at this level expect to train the right candidate on internal processes.
Which industries hire the most entry level regulatory affairs directors?
Entry Level regulatory affairs director roles concentrate in Biotechnology & Pharmaceuticals, Insurance, and Distribution & Wholesale, based on current listings on Migrate Mate as of August 2026. Those sectors drive entry level hiring because they face ongoing FDA, EMA, or ISO regulatory obligations that require dedicated compliance staff even at the junior level.