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Regulatory Affairs Compliance Specialist

Manchester Permanent View Job Description
An exciting opportunity has arisen for a Regulatory Affairs Compliance Specialist, who will be responsible for ensuring compliance with regulatory requirements and standards.
  • Fantastic opportunity to join a leading medical devices manufacturer
  • Fantastic opportunity to work with NPD lines

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

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

The Successful Applicant

A successful Regulatory Affairs Compliance Specialist should have:

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

What's on Offer

Competitive package available

Contact
Kelly Percival
Quote job ref
JN-012025-6655457
Phone number
+44 1727 730 143

Job summary

Job function
Life Sciences
Subsector
Regulatory Affairs
Sector
Healthcare / Pharmaceutical
Location
Manchester
Contract type
Permanent
Consultant name
Kelly Percival
Consultant phone
+44 1727 730 143
Job reference
JN-012025-6655457