Job Description

Kinetic has partnered with a leading Medical Device company who are hiring a Regulatory Affairs Assistant to be based in Plymouth.

Please note that you must meet all the criteria set out below for your application to be considered. Suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.

The main responsibilities will include but not limited to:

• Prepare, compile and submit regulatory approvals for various markets.
• Maintain and update existing product registrations, licenses, and regulatory certifications.
• Collaborate cross-functionally providing regulatory insights and responding to information requests.
• Monitor relevant industry-wide International Registration activities.
• Contribute to improving international registration procedures to enhance efficiency and compliance.

To be successful, you will need to meet the following:

• Bachelor’s degree in Life Sciences or equivalent.
• Minimum 1-2 years of experience in Regulatory Affairs within the Medical Devices industry in the UK.
• Good knowledge with key market approval requirements in APAC, EMEA, and LATAM regions.
• Strong organizational skills and attention to detail.
• Proficient in Microsoft Office Suite and document control systems.
• Applicants should be available for face-to-face interviews in the location mentioned above.

Must Read: Watch Out for These Red Flags Before You Hit Apply

Hiring? If you need help filling a similar position in your company, please contact us on +44 (0)208 137 0401 or click here.

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