QMS Engineer – Contract 📍 Bradford
🗓️ 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.
👉 Apply now