Regulatory Affairs Recruitment
What is Regulatory Affairs?
Regulatory Affairs experts deal with the regulations, laws, and guidelines that govern industries such as pharmaceuticals, medical devices, food and cosmetics, biologics, and veterinary products.
Additionally, it also involves coordinating and liaising with regulatory agencies to ensure compliance with regulatory requirements for drug or product development, clinical trials, approvals, and post-approval activities such as labelling, advertising, and manufacturing quality control.
Lastly, those working in this sector ensure that products are safe and effective for human use and are produced under safe and controlled conditions.
Our Experience
Scienta was built on a background of regulatory affairs recruitment, with our three founders working within the sector before deciding to start their own business.
Since then, we have continued to build our skills internally as well as our relationships with talent in the field. We now have a strong network of highly skills professionals as well as a team dedicated to hiring within regulatory affairs.
Key Roles We’ve Filled
Senior RA CMC Manager
Regulatory Affairs Specialist
Head of Regulatory
Current Regulatory Roles
Our Expert
Anthony Hughes
Principal Consultant
Regulatory Affairs
I help our clients across Europe find the best Regulatory talent to support their business.
Throughout my 9 year career in life science recruitment, I have continued to specialise within the Regulatory Affairs space. Due to this consistent focus, I have been able to build a strong talent pool of outstanding talent and have a deep understanding of the regulatory space.
Speak to Our Expert
Frequently Asked Questions
How to get into regulatory affairs
1. Get a relevant education: Firstly, it typically require a degree in a life science field such as biology, chemistry, or pharmacology.
2. Gain work experience: Start by getting an entry-level position in the pharmaceutical or medical device industry. Look for an opportunity to work in a regulatory department or a related area.
3. Consider specialised training: Some universities and organisations offer specialised training programs.
4. Obtain certification: Many professionals obtain certification from organisations such as the Regulatory Affairs Professional Society (RAPS) and the Association of Clinical Research Professionals (ACRP).
5. Network: Attend industry conferences, join professional organisations, and connect with other professionals to gain insights and get guidance.
6. Keep up-to-date: Lastly, it’s s a constantly evolving field, so it’s important to stay current on new regulations, guidelines, and best practices.
Is it worth getting a masters in Regulatory Affairs?
Getting a master’s can be worth it for individuals who want to advance their careers in the pharmaceutical, medical device, or biotech industries.
A master’s degree in this field can provide in-depth knowledge of regulations, policies, and industry practices, as well as analytical and critical thinking skills required for regulatory affairs roles.
Obtaining a master’s degree can also open up higher-paying jobs and career advancement opportunities in this field. However, one should weigh the costs and benefits of a master’s program before pursuing it.
