Quality System Coordinator - Medical Devices
Location: Falmouth Salary: £30,000 - £35,000 per annum
Sector: Pharmaceuticals, Medical Devices, Life Sciences Type: Contract
Contact: Lee Ashworth Job Published: 1 day ago
Quality System Coordinator (6-Month Fixed-Term Contract)
Location: Falmouth, Cornwall (4 days on-site, 1 day WFH)
Salary: £30,000 - £35,000 (depending on experience)
Are you an experienced Quality System professional with a background in the medical device industry? Do you have a passion for maintaining high-quality standards and ensuring compliance with international regulations? If so, we have a fantastic opportunity for you!
We are looking for a Quality System Coordinator to join a global IVF and reproductive genetics company based in Falmouth, Cornwall. This is a 6-month fixed-term contract role with a focus on maintaining and managing the Quality Management System (QMS), supporting the Quality Manager, and ensuring compliance with ISO 13485, FDA 21 CFR Part 820, and MDSAP standards.
Key Responsibilities:
* Support QMS activities: Assist in the creation, implementation, and maintenance of QMS to meet ISO 13485, FDA 21 CFR Part 820, MDSAP, and relevant regulations.
* CAPA Process: Help initiate, investigate, and implement corrective and preventive actions (CAPAs), ensuring timely resolution and tracking effectiveness.
* Non-Conformance Management: Maintain accurate records, perform trend analysis, and identify recurring issues through NCMRs.
* Audit Support: Prepare for and support internal and external audits, ensuring all documentation is up-to-date and compliant.
* Continuous Improvement: Identify opportunities for process improvements and track progress to meet quality objectives.
* Collaboration: Work closely with cross-functional teams and global stakeholders to align site-specific activities with global standards.
* Reporting: Generate reports and presentations for management reviews and audits related to CAPA, NCMRs, and Continuous Improvement.
Key Skills & Qualifications:
* Knowledge of regulatory standards: Solid understanding of ISO 13485, FDA 21 CFR Part 820, MDSAP, and EU Medical Device Regulations.
* Experience in Quality Systems: Minimum 2 years of experience in Quality Assurance, including document control, auditing, and CAPA management.
* Technical Skills: Proficient in Master Control and Microsoft Office Suite.
* Attention to Detail: Strong organizational and problem-solving skills, with a results-driven mindset.
* Audit Experience: Hands-on experience in auditing and knowledge of GMP.
Why Join Us?
* Flexible work environment: 4 days on-site and 1 day working from home.
* Be part of a dynamic, global company focused on cutting-edge IVF and reproductive genetics.
* Contribute to maintaining high standards of quality in an essential field.
If you have the skills and experience we are looking for, and you're ready to make an impact in a world-leading company, we'd love to hear from you! Apply now to join the team as a Quality System Coordinator.
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