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Lonza

Associate Principle QA Specialist

Reposted 3 Days Ago
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In-Office
Slough, Berkshire, England
Mid level
In-Office
Slough, Berkshire, England
Mid level
The Associate Principle QA Specialist will oversee QA activities, manage compliance issues, and mentor teams on GMP standards to ensure quality across studies and operations.
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Associate Principle QA Specialist

Location: Slough

This role plays a key part in maintaining high-quality standards across a wide range of studies and operational activities. You will help strengthen our culture of quality, support continuous improvement, and ensure that our processes meet GMP and global regulatory expectations.

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

What you will get

  • An agile career supported by a dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • A variety of benefits dependent on role and location

  • Explore all global benefits: https://www.lonza.com/careers/benefits

What you will do

  • Provide hands-on review, approval, and support for deviations, CAPAs, change controls, investigations, and OOS records

  • Review QA activities for MSAT studies, pilot studies, and development projects

  • Oversee QC activities, including method validation, reference standards, and stability studies

  • Manage and escalate critical compliance issues through the QMS

  • Perform audit trail reviews and lead area walkthroughs to identify and resolve compliance gaps

  • Audit raw data, protocols, and validation reports for GMP compliance

  • Support continuous improvement initiatives across Operations, QC, MSAT, and Development Services

What we are looking for

  • BSc/BEng in a scientific discipline or equivalent proven experience

  • Strong GMP expertise with practical experience in deviations, CAPAs, change control, investigations, audit trails, and data review

  • Hands-on QA skills, including the ability to provide real-time support across multiple teams

  • Experience maintaining inspection readiness and leading internal process audits

  • Ability to communicate clearly and mentor colleagues on GMP expectations and quality practices

  • A proactive, collaborative mindset with a commitment to quality and continuous improvement

  • Ability to work effectively in a fast-paced, cross-functional environment

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Top Skills

Gmp
Quality Management Systems (Qms)

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