At a Glance
- Tasks: Review batch documentation and ensure compliance with cGMP standards.
- Company: Lonza, a leading company in the biotech industry.
- Benefits: 12-month contract with opportunities for professional growth.
- Other info: On-site role with a focus on collaboration and continuous improvement.
- Why this job: Join a dynamic team and make a real impact on quality assurance.
- Qualifications: Experience in QA and knowledge of cGMP practices required.
The predicted salary is between 35000 - 42000 £ per year.
Lonza in Slough is seeking an experienced QA Associate to join the QA Operations team on a 12-month contract.
The role is site-based and focuses on batch documentation review and ensuring c GMP compliance across manufacturing, development and labs.
You will partner with Manufacturing, MSAT and Supply Chain, identify and escalate deviations and CAPAs, and coach shop-floor partners on c GMP best practices to maintain audit readiness and PQS performance.
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Senior QA Associate: Batch Review & Compliance (On-site) 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.
