Quality Engineering Optimisation Manager in Wales

The Opportunity

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world‑leading in vitro diagnostics company with award‑winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all.

Your new role

As the Quality Engineering Optimisation Manager, you will provide direction and operational oversight across Quality Engineering, ensuring alignment with global regulatory requirements (ISO 13485, FDA 21 CFR 820, IVDR, and other applicable standards). You will be responsible for leading and developing a team of Quality Engineers focused on continuous improvement and optimisation of manufacturing and quality processes for in vitro diagnostic (IVD) medical devices. The role ensures robust implementation of Corrective and Preventive Actions (CAPA), validation activities, and process improvement initiatives to maintain compliance with regulatory requirements while improving product quality, operational efficiency, and reliability.

The Quality Engineering Optimisation Manager works cross‑functionally to embed Quality and Compliance principles across the product lifecycle, supporting inspection readiness and operational excellence. Ensuring the team partners cross functionally to identify opportunities for improvement, drive root cause investigations, and implement sustainable solutions that enhance product and process performance.

What you’ll be doing

• People Leadership: 40%
  • Lead, develop, and inspire a team of Quality professionals to achieve organizational and individual performance objectives.
  • Establish clear priorities, assign responsibilities, and ensure effective resource allocation to meet business and compliance needs.
  • Coach and mentor emerging Quality leaders and technical experts to build organizational capability and ensure robust succession planning.
  • Model QuidelOrtho’s leadership principles by demonstrating collaboration, accountability, inclusion, and service mindset in all interactions.
• Quality Management System Oversight: 30%
  • Provide technical, regulatory, and operational leadership to ensure Quality systems comply with ISO 13485, FDA 21 CFR 820, and IVDR.
  • Partner with Manufacturing, R&D, Regulatory Affairs, Supply Chain, and other stakeholders to integrate Quality and Compliance principles throughout the product lifecycle.
  • Ensure the team maintains a state of inspection readiness and supports successful engagement with regulatory agencies, notified bodies, and internal audits.
  • Provides CAPA management within scope ensuring timely, effective investigation and resolution of quality issues.
  • Provides quality support and leadership for process, equipment and facility changes including validation support.
• Process Improvement: 30%
  • Support harmonization and standardization of Quality processes, procedures, and tools across sites and functions to strengthen compliance and efficiency.
  • Promote a culture of continuous improvement by identifying opportunities for simplification, process excellence, and digital enablement within the Quality Management System (QMS).
  • Monitor Quality performance using metrics and data analytics to identify risks, drive root cause analysis, and implement sustainable improvements.

What you’ll need to succeed

• Required Skills
  • Bachelor’s degree in Life Sciences, Engineering, or a related technical discipline required.
  • Demonstrated experience in Quality, Compliance, or related fields within the Medical Device, IVD, or Biopharmaceutical industries, including experience leading and developing teams.
  • Understanding of Quality System regulations and standards, including ISO 13485, FDA 21 CFR 820, and IVDR.
  • Proven ability to lead and develop high‑performing teams and build future technical and people leaders.
  • Demonstrated success driving Quality and Compliance initiatives that align with business strategy and regulatory expectations.
  • Excellent collaboration, influence, and communication skills across functional and organizational boundaries.
  • Strong analytical and problem‑solving skills, with experience using data to drive decision‑making and improvement.
  • Experience leading in a matrixed, global organization and managing competing priorities effectively.
• Preferred Skills
  • Advanced degree (MS, PhD, MBA, or equivalent) in a relevant discipline.
  • Experience implementing or optimizing global Quality Management Systems (QMS) and digital tools.
  • Lean Six Sigma, PMP, or similar certification demonstrating process improvement expertise.
  • Experience supporting or leading Health Authority or Notified Body inspections.

What we offer

• Competitive Salary
• Yearly Salary Reviews
• Attractive Pension Scheme
• Bonus Scheme
• Life Assurance
• Private Medical (If applicable)
• LinkedIn Learning
• Cycle to Work Scheme
• Free Onsite Gym
• Subsidised Canteen
• 25 days Holidays + 8 Bank Holidays
• Employee Assistance Programme
• Reward & Recognition Programmes
• State‑Of‑The‑Art facilities
• Exceptional career developmental prospects

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic.