Address
Form of work- Fantastic opportunity to be apart of a global Medical Device Business
- Great opportunity to be apart of a dynamic team working on exciting projects
About Our Client
The company is a well-established player and is a leading medical devices manufacturer renowned for its innovative solutions and exceptional quality of products. With a global presence and a significant employee base, the company is committed to creating a healthier and safer world.
Job Description
- Develop and implement regulatory strategies for new and modified products.
- Prepare and submit regulatory submissions to health authorities.
- Collaborate with global teams to ensure regulatory compliance.
- Manage regulatory aspects of product development and post-market activities.
- Lead interactions with regulatory agencies during pre and post-marketing phases.
- Monitor regulatory landscape and update teams on relevant changes.
- Ensure all documentation and reports comply with regulatory standards.
- Participate in quality assurance activities and internal audits.
The Successful Applicant
A successful 'Senior Regulatory Affairs Specialist' should have:
- A degree in Life Sciences, Pharmacy, or related field.
- Proven experience in Regulatory Affairs within a medical devices manufacturer.
- Strong knowledge of global regulatory requirements and procedures.
- Exceptional project management, communication, and analytical skills.
- Ability to work effectively in a team and independently
What's on Offer
- A competitive salary
- A supportive and collaborative company culture.
We are excited to welcome a new Senior Regulatory Affairs Specialist to our team. We encourage all eligible candidates to apply and contribute to our mission.
Contact
Kelly Percival
Quote job ref
JN-012024-6287902
Phone number
+44 1727 730 143
