Entry Level Senior Director Regulatory Affairs Jobs
New grad senior director regulatory affairs jobs welcome recent graduates and entry level candidates with zero to two years of experience, where strong internship work or a demonstrated understanding of regulatory frameworks can matter more than a long resume. Most openings are on-site roles across Biotechnology & Pharmaceuticals, Insurance, and Medical Devices, with employers like Oscar Health, Abbott, and BD hiring at this level now.
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Showing 4 of 31+ Entry Level Senior Director 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 Senior Director Regulatory Affairs Jobs: Frequently Asked Questions
How do I get an entry level senior director regulatory affairs job?
Start by building familiarity with regulatory submission processes, compliance documentation, and agency guidelines relevant to your target industry. Internships, co-ops, or coursework in regulatory affairs, life sciences, or quality assurance give you a concrete foundation. Employers at this level look for candidates who can demonstrate attention to detail, an understanding of regulatory pathways, and the ability to support senior staff on filings and reviews.
Which companies hire entry level senior director regulatory affairss?
Companies hiring entry level senior director regulatory affairss right now include Oscar Health, Abbott, and BD, based on current listings on Migrate Mate as of August 2026. Hiring at this level comes from a mix of established life sciences companies, medical device manufacturers, and specialty consulting firms that need support staff to assist with regulatory strategy and compliance workflows.
Are there remote entry level senior director regulatory affairs jobs?
Yes, though on-site and hybrid roles remain common at this level. About 35% of entry level senior director regulatory affairs openings are remote or hybrid as of August 2026, reflecting the nature of compliance work that often requires access to internal systems and close collaboration with cross-functional teams. Fully remote positions do exist, particularly at larger organizations with distributed regulatory departments.
Are these new grad senior director regulatory affairs jobs?
Yes, this page includes new grad, recent graduate, and junior senior director regulatory affairs roles alongside other entry level postings. A new grad friendly posting typically welcomes zero to two years of experience, accepts internship or co-op work in place of full-time history, and values a relevant degree or certification over a long employment record. Look for listings that mention training programs or mentorship as signals a new grad would be a strong fit.
Which industries hire the most entry level senior director regulatory affairss?
Entry Level senior director regulatory affairs roles concentrate in Biotechnology & Pharmaceuticals, Insurance, and Medical Devices, based on current listings on Migrate Mate as of August 2026. These sectors drive hiring at this level because regulatory compliance is built into their product development and market approval processes, creating a consistent need for entry level professionals who can support documentation, submissions, and cross-departmental coordination.