Regulatory Compliance Specialist - Medical Device

TN United Kingdom; Manchester; On-site; GBP 35,000 - 50,000; Full time

Job summary

A leading medical device manufacturer is seeking a Regulatory Compliance Specialist in Manchester. The role involves ensuring compliance with FDA regulations, managing documentation, and coordinating with internal teams. The ideal candidate will have a degree in Life Sciences and experience in regulatory affairs.

Qualifications

• Proven experience in regulatory affairs.
• Solid understanding of FDA regulations.
• Ability to manage multiple projects.

Responsibilities

• Ensure compliance with FDA regulations and standards.
• Manage all regulatory submissions and documentation.
• Liaise with external regulatory bodies.

Skills

Communication

Organisational skills

Attention to detail

Problem-solving

Education

Degree in Life Sciences

Job description

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Regulatory Compliance Specialist - Medical Device, Manchester

Client:

Page Personnel

Location:

Manchester, United Kingdom

Job Category:

Other

EU work permit required: Yes

Job Reference:

a228952bdfb5

Job Views:

3

Posted:

21.05.2025

Expiry Date:

05.07.2025

Job Description:

• Fantastic opportunity to join a leading medical devices manufacturer
• 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 an existing portfolio.

Job Responsibilities

• Ensure compliance with FDA regulations and standards
• Manage all regulatory submissions and documentation
• Liaise with external regulatory bodies
• Coordinate with internal teams to ensure company-wide compliance
• Stay up-to-date with changes in regulatory legislation and guidelines
• Contribute to the development of regulatory strategies
• Provide training and support to staff on regulatory issues
• Participate 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