At a Glance
- Tasks: Lead and improve our Quality Management System to ensure top-notch compliance.
- Company: Join Biocomposites, a global leader in innovative medical devices.
- Benefits: Enjoy competitive salary, company events, and employee discounts.
- Other info: Dynamic team culture with opportunities for growth and international travel.
- Why this job: Make a real impact in healthcare by enhancing quality and compliance.
- Qualifications: 6+ years in quality management within medical devices and strong communication skills.
The predicted salary is between 38250 - 46750 £ per year.
Job Description
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.
Job Summary
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 (e QMS).
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.
- Reports to
- Quality Manager
- Location & Working pattern
- Keele Office. Standard working hours (Mon – Fri, 8am-4pm or 9am-5pm, 35hpw)
Duties & Responsibilities
- Lead and maintain compliance with the organization's Quality Management System (QMS) and Electronic Quality Management System (e QMS).
- 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.
Essential requirements
- 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 ISO13485
- Lead auditor certification
- Experience with regulatory inspections and customer audits
- Familiarity with ERP and electronic document management systems
- Excellent communication skills
- People management skills
- Ability to take initiative within controlled working environment
- Ability to meet deadlines
- Attention to detail
Desirable requirements
- Level 5 in Leadership Management
- Member of a chartered institute
- Demonstrate positive and enthusiastic attitude
- Full, clean driving licence
What do we offer?
Competitive salary and benefits! With us, you will receive a competitive salary package and benefits.
We grow talent. At Biocomposites we create opportunities to thrive and grow.
One Biocomposites – team spirit & engagement.
Our culture is important and we strive to create engaged and inclusive global teams that encourage colleagues to share their diverse perspectives and opinions.
Who do we look for?
People who are passionate about what we do.
People who are open minded to evolving the way we work.
People who can work together to transform outcomes and change lives.
Benefits
- Company events
- Company pension
- Employee discount
- Free or subsidised travel
- Free parking
- On-site parking
- #J-18808-Ljbffr
Quality Compliance Lead in Keele employer: Biocomposites
Biocomposites in Keele, UK, is an excellent employer that prioritises collaboration and employee growth, making it an ideal place for those looking to advance their careers in a supportive environment. With a strong focus on safety and reliability, employees benefit from comprehensive training and development opportunities, ensuring they are well-equipped to lead maintenance activities effectively. Join us to be part of a dynamic team dedicated to innovation and excellence in the biocomposite industry.
