Regulatory Affairs Compliance Specialist

Michael Page (UK)
Manchester
GBP 35,000 - 60,000
Job description

Fantastic opportunity to join a leading medical devices manufacturer

About Our Client

My client is a leading medical device manufacturer within the beauty/tech space with innovative new product development lines and existing portfolio.

Job Description

  1. Ensuring compliance with FDA regulations and standards.
  2. Managing all regulatory submissions and documentation.
  3. Liaising with external regulatory bodies.
  4. Coordinating with internal teams to ensure company-wide compliance.
  5. Staying up-to-date with changes in regulatory legislation and guidelines.
  6. Contributing to the development of regulatory strategies.
  7. Providing training and support to staff on regulatory issues.
  8. Participating in audits and inspections.

The Successful Applicant

A successful Regulatory Affairs Compliance Specialist should have:

  1. A degree in Life Sciences or a related field.
  2. Proven experience in regulatory affairs.
  3. A solid understanding of FDA regulations and guidelines.
  4. Excellent communication and organisational skills.
  5. The ability to manage multiple projects simultaneously.
  6. Strong attention to detail and problem-solving abilities.

What's on Offer

Competitive package available.

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