Quality Systems & Document Control Specialist

Stryker Group; Belfast; On-site; GBP 30,000 - 40,000; Full time

Job summary

A global medical technology firm in Belfast is seeking a Quality Systems Specialist - Document Control. In this role, you will manage and maintain controlled documents ensuring compliance with FDA and ISO regulations. The ideal candidate has a Level 6 qualification and up to 2 years of experience. Responsibilities include administering the document control system and collaborating with cross-functional teams to support audits and ensure timely document approval. This role provides a hands-on opportunity in a fast-paced medical device environment.

Responsibilities

• Manage controlled documents to ensure compliance with regulations.
• Administer the document control system including revisions and approvals.
• Ensure compliance with ISO 13485 and other regulatory standards.
• Collaborate with teams for timely document approval and release.
• Facilitate internal and external audits.

Skills

Basic communication and project management skills

Strong interpersonal skills

Written and oral communication skills

Basic analytical skills

Basic problem-solving capabilities

Ability to work in cross-functional teams

Education

Level 6 qualification

Tools

Microsoft Office

MS Project

Adobe Acrobat

Job description

A global medical technology firm in Belfast is seeking a Quality Systems Specialist - Document Control. In this role, you will manage and maintain controlled documents ensuring compliance with FDA and ISO regulations. The ideal candidate has a Level 6 qualification and up to 2 years of experience. Responsibilities include administering the document control system and collaborating with cross-functional teams to support audits and ensure timely document approval. This role provides a hands-on opportunity in a fast-paced medical device environment.