Entry Level Regulatory Affairs Jobs
New grad regulatory affairs jobs welcome recent graduates and entry level candidates with zero to two years of experience, where strong internship work or coursework in compliance, quality, or life sciences can matter more than a long resume. Most openings are Biotechnology & Pharmaceuticals, Insurance, and Medical Devices roles with a mix of on-site, remote, and hybrid settings, and employers like Oscar Health, Abbott, and BD are hiring at this level now.
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Showing 4 of 31+ Entry Level Regulatory Affairs jobs
Job Title: Regulatory Affairs Associate I
Location: Skaneateles, NY - Fully Remote
Duration: 12 Months
Pay Rate Range:
Description: Responsible for the global coordination and the preparation of documents/packages for regulatory submissions. In this position you will also review and evaluate technical and scientific data and reports required for submission in support of global client’s products.
Top three to five technical skill requirements
- Familiar with USA and OUS device regulations (specifically EU device regulations)
- Experience with RA strategy development
- Experience with working with Cross functional team members
- Experience with interaction with external Regulators (FDA, TUV)
- Experience with working with medical devices
Essential Duties and Responsibilities
- Supports regulatory project plan execution
- Maintain awareness of regulatory requirements and ensure continued learning
- Maintain regulatory files in a format consistent with requirements
- Participate as an active team member of project teams as required
- Compile and prepare responses to questions from regulatory authorities according to plan
- Edit and proofread regulatory documentation
- Assist in preparation and review of labeling, SOP’s, and other departmental documents
- Compile under supervision regulatory documents for submission
- Track status and progress of regulatory documentation
- Understand Regulatory Affairs' position in small project teams
Qualifications
- Knowledge of regulations
- Scientific knowledge
- Administrative and project management skills
- Ability to contribute to multiple projects from a regulatory affairs perspective
- Ability to multitask and prioritize
- Interpersonal and communication skills
- Technical system skills (e.g. word processing, spreadsheets, databases, online research)
- Proofreading and editing skills
Education and/or Experience
- Bachelor’s degree or country equivalent in a relevant scientific discipline
- Suitable candidates with a non-scientific degree may be accepted and undertake further training e.g. under an apprenticeship or similar post graduate qualification
- Regulatory experience (not mandatory) preferably within a healthcare environment
Job Title: Regulatory Affairs Associate I
Location: Skaneateles, NY - Fully Remote
Duration: 12 Months
Pay Rate Range:
Description: Responsible for the global coordination and the preparation of documents/packages for regulatory submissions. In this position you will also review and evaluate technical and scientific data and reports required for submission in support of global client’s products.
Top three to five technical skill requirements
- Familiar with USA and OUS device regulations (specifically EU device regulations)
- Experience with RA strategy development
- Experience with working with Cross functional team members
- Experience with interaction with external Regulators (FDA, TUV)
- Experience with working with medical devices
Essential Duties and Responsibilities
- Supports regulatory project plan execution
- Maintain awareness of regulatory requirements and ensure continued learning
- Maintain regulatory files in a format consistent with requirements
- Participate as an active team member of project teams as required
- Compile and prepare responses to questions from regulatory authorities according to plan
- Edit and proofread regulatory documentation
- Assist in preparation and review of labeling, SOP’s, and other departmental documents
- Compile under supervision regulatory documents for submission
- Track status and progress of regulatory documentation
- Understand Regulatory Affairs' position in small project teams
Qualifications
- Knowledge of regulations
- Scientific knowledge
- Administrative and project management skills
- Ability to contribute to multiple projects from a regulatory affairs perspective
- Ability to multitask and prioritize
- Interpersonal and communication skills
- Technical system skills (e.g. word processing, spreadsheets, databases, online research)
- Proofreading and editing skills
Education and/or Experience
- Bachelor’s degree or country equivalent in a relevant scientific discipline
- Suitable candidates with a non-scientific degree may be accepted and undertake further training e.g. under an apprenticeship or similar post graduate qualification
- Regulatory experience (not mandatory) preferably within a healthcare environment
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Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals11
- Insurance5
- Medical Devices3
- Healthcare & Medical Services3
- Education2
Entry Level Regulatory Affairs Jobs: Frequently Asked Questions
How do I get an entry level regulatory affairs job?
Employers hiring at the entry level look for coursework or internships in regulatory science, quality assurance, or a life sciences field, along with familiarity with submission processes and agency guidelines. Candidates who can show hands-on exposure through a co-op, capstone project, or lab role stand out. Tailoring your resume to highlight compliance or documentation experience, even from academic settings, gives you a real edge.
Which companies hire entry level regulatory affairss?
Companies hiring entry level regulatory affairss right now include Oscar Health, Abbott, and BD, based on current listings on Migrate Mate as of August 2026. Hiring covers pharmaceutical manufacturers, medical device companies, contract research organizations, and biotech startups, many of which actively recruit new graduates into structured regulatory associate or coordinator roles.
Are there remote entry level regulatory affairs jobs?
Yes, though most entry level roles still favor on-site or hybrid arrangements given the hands-on training involved. About 35% of entry level regulatory affairs openings are remote or hybrid as of August 2026, so there are genuine options for candidates who need flexibility, particularly at larger organizations with established remote onboarding programs.
Are these new grad regulatory affairs jobs?
Yes, the listings here include new grad, recent graduate, and junior regulatory affairs roles. A posting is new-grad friendly when it welcomes zero to two years of experience, accepts internships or co-ops in place of full-time history, or calls out a life sciences degree as sufficient qualification. If a role says entry level or regulatory associate, it is open to candidates coming directly from school.
Which industries hire the most entry level regulatory affairss?
Entry Level regulatory affairs roles concentrate in Biotechnology & Pharmaceuticals, Insurance, and Medical Devices, based on current listings on Migrate Mate as of August 2026. Those sectors drive hiring at this level because they face ongoing submission, labeling, and compliance requirements that create steady demand for junior regulatory staff supporting senior teams.