Quality Assurance System Manager

United Kingdom, Slough

Job Title: Quality Assurance System Manager

Location: Slough, Hybrid

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising. ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Lonza Slough was the first multi-product licensed contract manufacturing facility to be licensed by the. FDA, with its original Establishment License for the production of monoclonal antibodies first granted in 1985.

https://www.youtube.com/watch?v=wZaXzPKWEv0&list=PLh3u2rKfWyIfXC2d2O3enUrpMjjJ7DO_x&index=18

What You Will Get

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• A variety of benefits dependant on role and location
• The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits
  
  

What you will do:

• Your work will directly contribute to improving patient outcomes and global health
• Lead a team of up to 10 to ensure our GMP (Good Manufacturing Practice) biotech facilities meet USFDA and European standards
• Apply GMP (Good Manufacturing Practice) regulations consistently. Use your quality expertise to drive continuous PQS (Pharmaceutical Quality System) improvements
• Maintain the PQS in line with global quality systems, Lonza standards, and current regulations
• Monitor PQS performance metrics and implement improvements based on data insights
• Oversee training programs to ensure compliance with GMP and Lonza's global standards
• Collaborate with site leaders to align training with quality and business goals
• Ensure smooth implementation of training programs across the site
  
  

What we are looking for:

• People Management experience is highly recommended for this role
• Significant experience working in QA roles within GMP-regulated pharmaceutical environments, ideally in biologics or bio-pharmaceuticals
• Proven experience managing regulatory inspections (e.g., MHRA, FDA)
• Excellent knowledge of Trackwise is essential for this role
• Experience and knowledge of using learning and development software, preferably Cornerstone
  
  

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business. results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return,. we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin,. sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R69198

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