At a Glance
- Tasks: Review batch documentation and ensure compliance in a dynamic manufacturing environment.
- Company: Join Lonza, a global leader in life sciences with a collaborative culture.
- Benefits: Competitive hourly rate, inclusive workplace, and agile career opportunities.
- Other info: Be part of a diverse team dedicated to improving lives through innovation.
- Why this job: Make a real impact on medicine quality and safety while working closely with teams.
- Qualifications: 5+ years in Quality Assurance within cGMP, with strong attention to detail.
The predicted salary is between 40000 - 50000 £ per year.
Are you an experienced Quality Assurance professional looking to make a direct impact on the shop floor of a global life sciences leader?
We are looking for a QA Associate to join our dynamic QA Operations team in Slough for a 12-month contract, supporting sitewide batch review and compliance!
This is a fully site‑based role.
Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get
- An agile career and dynamic working culture.
- An inclusive and ethical workplace.
- Competitive hourly rate.
The hourly rate for this position in the United Kingdom is expected to range between 17.00£ and 19.00£.
Initial salary placement within this range will be determined based on role‑related factors such as experience, qualifications, and expected contribution.
What you will do
- Deliver shoulder-to-shoulder batch documentation review across manufacturing, development, and laboratory operations.
- Partner directly with Manufacturing, MSAT, and Supply Chain teams to ensure right-first-time document completion.
- Identify non-conformances and manage/escalate major compliance issues through the site QMS (deviations, CAPAs).
- Serve as an operational QA point of contact, driving adherence to site PQS and c GMP guidelines.
- Coach and mentor shop-floor partners in c GMP best practices to maintain a state of continuous audit readiness.
- Participate actively in site governance and PQS continuous improvement initiatives.
What we are looking for
- At least 5 years of Quality Assurance (QA) experience gained within a c GMP manufacturing environment.
- Direct experience reviewing batch records and managing QMS processes (deviations, CAPAs, non-conformances).
- Educational background in Science (BSc in Biology or related field) or equivalent industry experience.
- Outstanding attention to detail, organizational agility, and ability to manage strict deadlines.
- Excellent verbal and written English communication skills for effective stakeholder management.
- 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.
As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.
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Quality Assurance Associate in Slough employer: Lonza
Lonza is an exceptional employer, providing a vibrant work culture in Cambridge where innovation thrives. Employees benefit from a competitive package and ample opportunities for professional growth, all while contributing to groundbreaking advancements in therapies that impact patients worldwide.
