About this role
QA PM I – Operations
Portsmouth, New Hampshire — Onsite, 5 days per week
As a QA PM I in our Portsmouth, NH site, you will play a key role in supporting our customers and internal teams by ensuring quality and compliance standards are met. This role offers the opportunity to collaborate across diverse functions and contribute to the delivery of life‑changing therapies.
What you will get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
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.
Support change controls, deviations, investigations, CAPAs and quality‑related documentation.
Lead Joint Quality Team meetings and track actions, minutes and KPIs.
Collaborate with MSAT, Manufacturing, Engineering and QC teams.
Review quality documents such as Quality Agreements and Product Quality Reviews.
Ensure sound scientific justification and data integrity across quality records.
Support customer audits and routine quality activities.
What we are looking for:
Bachelor’s degree in a scientific discipline or equivalent experience.
Experience working in a GMP environment.
Foundational understanding of quality assurance principles.
Strong communication and collaboration skills.
Ability to manage multiple priorities effectively.
Attention to detail and a mindset focused on continuous improvement.
Ability to build strong working relationships with internal teams and external partners.
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.
Other facts
About Lonza
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
What you'll do
- Serve as the primary QA liaison for assigned external customers and support change controls, deviations, investigations, CAPAs, and quality-related documentation. Collaborate with various teams and ensure compliance with quality standards.
Ready to join Lonza?
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