QA PM II-Operations
About The Position
Join Lonza’s Quality Operations team and play a key role in ensuring compliance and excellence for our customers. As a QA Project Manager II, you will act as the primary liaison for quality-related matters, driving collaboration and delivering solutions that make a real impact. What you will get: An agile career and dynamic working culture An inclusive and ethical workplace Competitive compensation programs that recognize high performance Medical, dental, and vision insurance Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits What you will do: Serve as the primary QA liaison for assigned external customers Manage quality processes including change controls, deviations, investigations, and CAPAs Lead Joint Quality Team meetings and track action items Review and approve investigation reports and root cause analyses Collaborate with internal teams such as MSAT, Manufacturing, Engineering, and QC Support customer audits and maintain compliance with data integrity principles Prepare and present customer metrics and KPIs What we are looking for: Bachelor’s degree in a scientific field or equivalent experience Experience in GMP environments and Quality Assurance (5+ years preferred) Strong understanding of biotechnology manufacturing and project management Ability to analyze data, make sound decisions, and prioritize tasks Excellent communication and relationship-building skills Familiarity with cGMPs and regulatory requirements A proactive, detail-oriented approach with a commitment to quality 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 offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. 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.
Requirements
- Bachelor’s degree in a scientific field or equivalent experience
- Experience in GMP environments and Quality Assurance (5+ years preferred)
- Strong understanding of biotechnology manufacturing and project management
- Ability to analyze data, make sound decisions, and prioritize tasks
- Excellent communication and relationship-building skills
- Familiarity with cGMPs and regulatory requirements
- A proactive, detail-oriented approach with a commitment to quality
Responsibilities
- Serve as the primary QA liaison for assigned external customers
- Manage quality processes including change controls, deviations, investigations, and CAPAs
- Lead Joint Quality Team meetings and track action items
- Review and approve investigation reports and root cause analyses
- Collaborate with internal teams such as MSAT, Manufacturing, Engineering, and QC
- Support customer audits and maintain compliance with data integrity principles
- Prepare and present customer metrics and KPIs
Benefits
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Competitive compensation programs that recognize high performance
- Medical, dental, and vision insurance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
