Life Science
Regulatory Affairs Jobs
Helping you navigate your next career move in Regulatory Affairs. Discover roles with pharmaceutical, biotech and medical device leaders across the globe.
Your Regulatory Affairs Career Starts Here
Regulatory Expertise We Recruit Into
Explore opportunities across specialist regulatory disciplines, product categories and therapeutic areas within the global life sciences sector.
Chemistry, Manufacturing & Controls (CMC)
Regulatory professionals working in CMC handle the technical backbone of a submission, manufacturing changes, specifications and stability packages, partnering with quality and technical teams to keep global filings on track.
Labelling, Packaging & Promotional Compliance
This discipline covers the approval of product labelling, packaging artwork, and promotional material, requiring close attention to regional rules and close coordination with marketing, legal, and medical colleagues.
Medical Devices & In Vitro Diagnostics
Device-focused regulatory specialists build submission strategies for implantable, diagnostic, and digital health products, drawing on knowledge of frameworks such as the EU MDR, the IVDR, and the FDA's 510(k) pathway.
Oncology
Submissions for cancer therapies span solid tumours, blood cancers and targeted treatments, often moving through accelerated pathways and demanding close, ongoing dialogue with regulators.
Rare & Orphan Diseases
Filings for small patient populations frequently rely on orphan designations and adaptive approval pathways, with regulatory teams working hand in hand with agencies on unconventional submission strategies.
Vaccines & Public Health
Large-scale licensure programmes for preventive and therapeutic vaccines tend to run on compressed timelines, requiring coordinated global filing strategies and strong relationships with public health authorities.
Cell & Gene Therapy
Regulatory strategy for CAR-T, gene editing and regenerative medicines sits at the sharp end of the industry, where guidance is still evolving and agency dialogue happens early and often.
Immunology & Biologics
Filings for autoimmune and inflammatory disease treatments, covering conditions like rheumatoid arthritis, psoriasis and IBD, involve dense clinical data packages and an increasingly active biosimilar landscape.
Pharmacovigilance & Regulatory Compliance
Once a product is approved, this discipline keeps it there by managing periodic safety reporting, variations, and lifecycle commitments that protect both patients and ongoing market authorisation.
Regulatory Strategy & Product Development
Support products from early development through to marketing authorisation, helping organisations navigate global regulatory requirements and build effective submission strategies.
International Regulatory Affairs
Manage submissions and compliance activities across multiple global markets, including the UK, Europe, US and emerging regions, ensuring products meet local regulatory requirements.
Advertising & Promotional Review
Review promotional materials and marketing communications to ensure regulatory compliance while supporting commercial objectives.
Regulatory Affairs Jobs We Recruit For
Regulatory Affairs professionals play a vital role in bringing medicines, medical devices and healthcare products to market. They help organisations navigate complex regulatory requirements, manage submissions to health authorities and ensure products remain compliant throughout their lifecycle.
At Orion, we recruit for a wide range of Regulatory Affairs jobs across the life sciences sector, including:
Regulatory Affairs Associate
A Regulatory Affairs Associate supports the preparation and maintenance of regulatory submissions, helping organisations meet global compliance requirements and approval timelines.This is often the starting point for professionals exploring Regulatory Affairs Associate jobs and building long-term careers in Regulatory Affairs.
Regulatory Affairs Specialist
A Regulatory Affairs Specialist manages regulatory activities across product development and commercialisation, supporting submissions, agency interactions and compliance initiatives. Regulatory Affairs Specialist jobs are among the most sought-after opportunities across the life sciences industry.
Regulatory Affairs Manager
Senior professionals lead complex submissions, provide regulatory guidance to cross-functional teams and help shape regulatory strategy across multiple products and markets.
Regulatory Affairs Director
A Regulatory Affairs Director oversees regulatory strategy at an organisational level, managing agency relationships, global submissions and long-term compliance objectives.
Labelling & Submissions Specialist
Labelling and Submissions Specialists focus on the preparation, review and maintenance of product labelling, packaging content and regulatory documentation across international markets.
Regulatory Affairs Consultant
Regulatory Affairs Consultants provide specialist expertise on a contract or project basis, advising organisations on submissions, regulatory strategy and compliance requirements.
CMC Regulatory Affairs Specialist
CMC Regulatory Affairs professionals manage submissions relating to manufacturing processes, product specifications and regulatory changes throughout the product lifecycle.
Medical Device Regulatory Affairs Specialist
These professionals support regulatory strategy and submissions for medical devices and diagnostics, working with frameworks such as EU MDR, IVDR and FDA requirements.
Benefits Of Working In Regulatory Affairs
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1. Strong Earning Potential, Permanent or Contract
Regulatory expertise is scarce and well rewarded, with day rates for experienced contractors holding up well against other life sciences disciplines.
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2. A Genuine Upward Career Path
Build a structured career path with opportunities to progress from Regulatory Affairs Associate and Specialist roles through to management and leadership positions.
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3. Real Influence Over What Reaches Patients
Support the approval and lifecycle management of medicines, medical devices and healthcare products that improve patient outcomes worldwide.
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4. Demand That Isn't Going Away
Every regulated product needs regulatory oversight, which keeps Regulatory Affairs recruitment active across pharma, biotech, device and CRO employers alike.
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5. More Flexibility Than People Expect
Many Regulatory Affairs jobs now offer hybrid and remote working arrangements, particularly within submissions, labelling and lifecycle management functions.
Featured Life Science Jobs
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FAQs about Clinical Research Associate Jobs
What qualifications do I need to work in Regulatory Affairs?
Most Regulatory Affairs jobs require a life sciences degree in subjects such as pharmacy, chemistry, biology or biomedical science. Employers also value experience in areas such as quality assurance, clinical operations, scientific writing and compliance. Knowledge of regulatory frameworks including FDA, EMA and MHRA requirements can be beneficial, particularly for more senior roles.
What kind of salary can I expect in Regulatory Affairs?
Regulatory Affairs professionals can typically expect salaries ranging from around $50,000–$80,000 for entry-level and Associate roles, $80,000–$130,000 for Specialist and Manager positions, and $150,000+ for senior leadership roles. Salaries vary by location, experience level and specialism, while contractors and consultants can often command premium rates, particularly in high-demand areas such as oncology, medical devices and cell and gene therapy.
Are Regulatory Affairs jobs available remotely?
Many Regulatory Affairs jobs now offer hybrid or remote working arrangements, particularly within submissions, labelling and lifecycle management functions. Working arrangements vary by employer, product type and regulatory responsibilities.
What are the most in-demand areas of Regulatory Affairs?
Demand remains strong across areas including oncology, medical devices, cell and gene therapy, CMC, pharmacovigilance and rare diseases. As regulatory requirements continue to evolve globally, employers are increasingly seeking professionals with specialist expertise.
How can Orion Group help me find Regulatory Affairs jobs?
Our specialist Life Sciences recruiters work closely with pharmaceutical, biotechnology, medical device and CRO organisations worldwide. Whether you're looking for your first Regulatory Affairs Associate job or your next leadership opportunity, we can provide access to relevant roles, market insights and ongoing career support throughout your job search.
What experience do I need for Regulatory Affairs Specialist jobs?
Most Regulatory Affairs Specialist jobs require experience in regulatory submissions, compliance or related life sciences functions. Employers typically look for professionals with a strong understanding of regulatory requirements and experience supporting product approvals or lifecycle management.
Is contracting a good career option in Regulatory Affairs?
Yes. Many Regulatory Affairs professionals build successful long-term careers through contracting, benefiting from flexible working arrangements, varied project experience and strong earning potential across the life sciences sector.
Apply for Regulatory Affairs Jobs with Orion Group
Whether you’re a graduate starting out or a senior professional ready for your next move, Orion can help you find the right role.
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