Quality Compliance Lead

Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries.

Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world.

Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries.

Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world.

The Quality Compliance Lead is responsible for developing, implementing, maintaining, and continuously improving the organization's Quality Management System (QMS) and Electronic Quality Management System (eQMS). This role ensures compliance with applicable regulatory requirements, industry standards, and internal quality policies. Working closely with cross-functional teams, the Quality Compliance Lead promotes a culture of quality and drives continuous improvement to strengthen quality performance and reduce compliance risk.

Quality Manager

Keele Office. Standard working hours (Mon - Fri, 8am-4pm or 9am-5pm, 35hpw)

• Lead and maintain compliance with the organization's Quality Management System (QMS) and Electronic Quality Management System (eQMS).
• Ensure adherence to applicable regulatory requirements, customer standards, and industry regulations (ISO 13485, MDSAP, GMP, FDA, or other relevant standards).
• Plan, coordinate, and lead internal quality audits and support external audits, customer audits, and regulatory inspections.
• Plan, coordinate, and lead any supplier audits.
• Monitor compliance against quality procedures, policies, and regulatory requirements, identifying areas for improvement.
• Monitor quality system performance through key performance indicators (KPIs) and report trends to management.
• Review and approve quality documentation, ensuring adherence to applicable regulatory requirements, customer standards, and industry regulations (ISO 13485, MDSAP, GMP, FDA, or other relevant standards).
• Drive continuous improvement initiatives using quality improvement methodologies.
• Deliver quality training and promote awareness of quality system requirements throughout the organization.
• Maintain quality records and ensure document retention requirements are met.
• Stay informed of changes to relevant regulations and quality standards.
• Management and Development of a team
• Role will require some travel nationally and internationally.

• Level 6 within a science regulated industry or relevant experience
• Minimum 6 years quality management experience within Pharmaceutica/Medical Devices
• Knowledge of Quality Management Systems ISO
  13485
• Lead auditor…