- Quality Management: Maintain and uphold QMS standards (ISO 13485, 9001 etc.)
- Investigations: Conduct thorough quality and engineering investigations using cutting-edge tools and techniques.
- Inspections: Perform meticulous inspections of incoming materials, in-process items, and finished products.
- Documentation: Create and review cGMP documentation, ensuring everything is up to snuff.
- Customer Interaction: Be the friendly face and knowledgeable point of contact for all customer quality concerns.
- Experience: Ideally, you've got a background in the medical device industry, but experience in automotive or aerospace will also shine.
- Skills: You're strategic, methodical, and detail-oriented. Your communication skills are top-notch, and you can read and interpret complex specifications with ease.
- Independence: You work well independently, managing your time effectively and meeting tight deadlines.
- Knowledge: Familiarity with ISO 13485, cGMP/FDA standards, and other related directives is a big plus.
- Right to Work in the UK
- Impact: Directly influence the quality of products that make a real difference.
- Growth: Continuous learning and development in current quality principles.
- Team: Join a supportive and professional team dedicated to excellence.