At a Glance
- Tasks: Ensure GMP quality and compliance while collaborating with various teams for continuous improvement.
- Company: Lonza Group Ltd., a leader in biopharmaceutical process development.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Exciting career opportunities in a fast-paced environment.
- Why this job: Join a dynamic team and make a real impact on biopharmaceutical quality assurance.
- Qualifications: Experience in QA, GMP compliance, and strong collaboration skills.
The predicted salary is between 50000 - 65000 £ per year.
Lonza Group Ltd. in Slough is seeking a Senior Quality Assurance Specialist to support the Centre of Excellence for biopharmaceutical process development and GMP manufacturing.
You will ensure GMP quality and compliance across the site, providing expert QA oversight through QMS, governance, and quality leadership.
The role collaborates with GMP Manufacturing, Quality Control, MSAT, Procurement, and Warehouse to uphold regulatory standards and drive continuous improvement.
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Senior QA Specialist: GMP Compliance & Process Quality in Slough employer: Lonza Group Ltd.
At Lonza, we pride ourselves on being an excellent employer, offering a dynamic working culture that fosters collaboration and innovation in our Slough laboratory. Our commitment to employee growth is reflected in our agile career paths and comprehensive benefits, ensuring that every team member feels valued and supported in their professional journey. Join us to be part of a diverse and inclusive workplace where your contributions directly impact the future of medicine.
