Job Title: Regulatory Affairs Manager - Medical Devices
Location: Hertfordshire
Hybrid Working - 2/3 days office based
Salary: 50,000 - 70,000 plus package (Flexible dependant on experience)
Exciting opportunity to join a growing R&D focused pharmaceutical manufacturer, specialised within the OTC and Prescription market for topical products.
This role will be responsible for managing and motivating a small regulatory team, and guiding the business through the new regulatory MDD/MDR changes, ensuring the business remains compliant in all aspects.
Role:
- Preparation and submission of medical device technical files
- Provide regulatory expertise in all aspects of product regulatory compliance, and maintenance of certifications
- Maintenance of accurate technical documentation
- Manage and motivate a small regulatory team
Experience:
- Pharma/Medical Device/OTC/Cosmetics background within Regulatory Affairs
- Strong understanding of MDD/MDR regulations
- Experience authoring technical documentation
- Leadership qualities, effective communicator, and ability to motivate
For more details please apply with your update CV and I will be in touch to discuss further details. - chris.bart@cpl.com
- Agency: Cpl Life Sciences
- Reference: JO-2205-492721
Website: Cpl Life Sciences
- Posted: 25th July 2022
- Expires: 22nd August 2022
