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Regulatory Affairs Manager

Hertfordshire   •  Negotiable  •  Permanent, Full time


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
  • Posted: 25th July 2022
  • Expires: 22nd August 2022

Cpl Life Sciences

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