Lonza
Senior QA Specialist - Night Shift
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Senior Quality Assurance Specialist
Location
Slough
Shift Pattern
4 days on followed by 4 days off, 6pm to 6am
About the Role
We are currently looking for an experienced Senior Quality Specialist to join our Centre of Excellence for biopharmaceutical process development and small-scale GMP manufacturing in Slough, UK.
You will enable site operations performance by managing and supporting GMP issues through QMS processes, site governance, and senior QA Leadership. Support Engineering, Validation, Supply Chain, Procurement, and Warehouse functions at Slough site for all Quality Assurance related elements.
What You Will Get
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- A variety of benefits dependant on role and location
The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits
Key Responsibilities
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- To provide shoulder to shoulder review, approval, and support for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations
- Utilise knowledge of GMP and quality processes within the functional areas to Manage and escalate Major and Critical compliance issues through the site QMS processes e.g. deviations and CAPAs
- To actively identify, suggest, and participate in continuous improvement activities
- Mentor and coach business partners in cGMP practices to maintain and develop a cGMP environment
- Maintain and promote a state of audit readiness
- Actively suggest, initiate, participate, and contribute to PQS process improvements initiatives and projects
- Provide QA SME support at departmental Local Quality Councils and project meetings
- Provide shoulder to shoulder review, approval, and QA Technical support to key business partners for the management of quality records e.g. Deviations, CAPA, Change Controls, Investigations
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What We Need You to Have
- BSc life Sciences qualified
- Significant experience within Quality Assurance
- Hands-on experience with CAPA’s and Deviations
- Will ideally have a background within Engineering, Warehousing, or Validation
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.
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.
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