Join Our Team as a QA Specialist!
Are you ready to take the lead in Quality Assurance at one of the world’s leading pharmaceutical manufacturers?
We are looking for a Principal QA Specialist to oversee the Pharmaceutical Quality System (PQS), drive continuous improvements, and ensure compliance with both Lonza and regulatory standards based in our facility in Slough.
In this role, you will:
🔹 Lead the PQS: Oversee the Pharmaceutical Quality System, ensuring its efficiency, compliance, and fitness for purpose. 🔹 Strategic Oversight: Provide expertise in managing GMP issues, escalating quality concerns, and resolving complex quality challenges. 🔹 Continuous Improvement: Champion innovation and contribute to quality improvements that enhance operational excellence. 🔹 Collaborate with Global Teams: Represent the site in global meetings, coordinate communications, and manage internal issues. 🔹 Compliance & Training: Ensure regulatory compliance, drive GMP training initiatives, and maintain inspection readiness.
What We’re Looking For:
* Degree: BSc in Science or Quality Assurance discipline.
* Experience: Minimum 5 years in the pharmaceutical industry, with at least 2 years in deviation management and QA roles.
* Skills: Strong experience in PQS design, implementation, and management. Lead Investigator qualification or equivalent is a plus.
* On-Site: This is a full-time, 5 days a week on-site position at our Slough facility.
Why Join?
* Be part of a globally recognized leader in healthcare manufacturing.
* Shape and influence the quality strategy at the site level.
* Work in a dynamic, supportive environment where your expertise truly matters.
If you’re ready to make a real impact in quality assurance and work at the forefront of pharmaceutical excellence, we’d love to hear from you!
Apply today or connect for more details.
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