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Compliance / Quality Administrator - Medical Devices

Posted 24 days ago

  • London, Greater London
  • Any
  • External
  • Expired - 2 months ago
Compliance / Quality Administrator Medical Devices We are looking for a Compliance / Quality Administrator to join a dynamic company developing an array of products for the medical and healthcare industry. The company is growing and offering many opportunities for personal career development in addition to a wide variety of new projects to work on. As the Compliance / Quality Administrator you will join their Product Management Team and will be responsible for document control in compliance with applicable regulatory standards. The job will suit a friendly, diligent and motivated individual with a background in Quality Assurance / Quality Management /Document Control or similar technical administration role within medical equipment sector. Compliance / Quality Administrator s Responsibilities:
Producing, updating and maintaining product specifications and design documentation, making sure that all documentation complies with internal procedures and International Standards. Manage product changes, resolving design and build issues while collaborating with global supplies and distribution partners. Assist with quality control of products. Management of documentation control system Manage medical device technical files and documentation for new products, working closely with Sales and Purchasing to resolve technical questions.
Requirements:
Experience in document control for ISO9001 Quality Management System and understanding of medical regulatory standards. Excellent computer literacy with proficiency in Microsoft Office products is essential (especially Word and Excel). NetSuite and/or DemandCaster experience is desirable. Quality Data reporting and analysis. Excellent written and verbal communication skills and attention to detail are essential.
Vacancy Location: West Cambridgeshire (Commutable from Cambridge, St Neots, Letchworth, Hitchin, Bedford, Huntingdon, etc.)
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