QMS Engineer – Contract
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Bradford
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6-Month Contract
About the Role:
We're currently looking for an experienced
QMS Engineer
to support a key project within an
engineering manufacturing environment
based in
Bradford
- This is a fantastic contract opportunity for a quality professional with hands-on experience in quality management systems and regulatory standards within the medical device sector.
Key Responsibilities:
- Implement and manage Quality Management Systems (QMS) in line with business and regulatory requirements.
- Develop and maintain procedures, work instructions, and quality documentation.
- Plan, perform, and report on internal audits to ensure compliance and drive continuous improvement.
- Support cross-functional teams to maintain quality standards and regulatory compliance across manufacturing processes.
- Ensure alignment with ISO 13485, UK MDR 2002, and EU MDR requirements.
About You:
- Proven experience working as a QMS Engineer or in a similar quality-focused role within an engineering manufacturing environment.
- Strong knowledge of quality management systems and internal auditing processes.
- Familiarity with medical device and regulatory standards including ISO 13485, UK MDR 2002, and EU MDR.
- Excellent attention to detail with strong organisational and communication skills.
- Able to work independently and collaborate effectively with operational and engineering teams.
Contract Details:
- 6-month contract
- Bradford-based
- Competitive day rate available
- Immediate start preferred
Interested?
If you're a proactive
QMS Engineer
with experience in engineering manufacturing and medical device regulations, we'd love to hear from you.
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Apply now