Job Description

You are responsible for ensuring all Systems managed and coordinated by the Quality department are maintained and compliant. You will have strong attention to detail and a working understanding of medical device requirements. This position works directly with site manufacturing, supply chain and distribution in assuring compliance for incoming and outgoing material, as well as adherence to the Quality Management System throughout the business.

To be considered for the role, candidates would need to have a minimum of 1 years’ experience in a Quality based role in Medical Devices, Pharmaceuticals or Cosmetics. Experience of working with Quality Systems such as CAPA, Complaints and Supplier Management is essential. Previous experience working in a cGMP or ISO 13485 regulated environment, is also essential. Applicants will ideally be educated to degree level in a scientific subject (e.g., Chemistry). Formal auditor training such as Internal or Lead Auditor in ISO 13485 or 9001 would be advantageous.

Required Knowledge, Skills, and Abilities