
location_on12, Summer Street, North End, Portsmouth, Rockingham County, New Hampshire, 03801, United States
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 you will be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
As a Deviation Investigation Supervisor, you will lead a team of investigators, driving the timely, high-quality completion of deviation investigations while fostering a culture of compliance, accountability, and continuous improvement. This role plays a critical leadership function in aligning team performance with departmental and site goals, ensuring strict adherence to cGMP standards and regulatory expectations.
You will partner cross-functionally with Manufacturing, Quality, and other stakeholders to support investigations and drive deviation reduction. Your day will involve facilitating key meetings, including daily management system sessions and deviation review boards, while providing technical guidance and escalation management for complex investigations.
This position is based in our Portsmouth, NH office. The typical work schedule is Monday through Friday, 8:00 AM–5:00 PM EST.
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.
Ready to shape the future of life sciences? Apply now.
Work model: On-site
12, Summer Street, North End, Portsmouth, Rockingham County, New Hampshire, 03801, United States
Portsmouth, New Hampshire
Skills: CGMP, Fda, Ema, Ich, Ich Q9, Quality Risk Management, Fmea, Haccp, Fishbone, What-If Analysis.
Education: Bachelor's degree in Life Sciences, Engineering, or related field required.
Advanced degree in Life Sciences, Engineering, or a related field.
Lonza, headquartered in Basel, Switzerland, operates as a pioneering contract development and manufacturing organization within the pharmaceutical manufacturing industry. Established in 1897, the company transformed into the original CDMO and continues to leverage cutting-edge science, smart technology, and lean manufacturing to convert customer innovations into viable therapies. As one of the largest Western CDMOs, Lonza provides comprehensive, integrated solutions designed to address complex client needs across the global healthcare sector.
The organization supports a vast network of approximately 18,500 colleagues spread across five continents, working together to deliver life-enhancing and life-saving treatments to market with speed and scale. This global footprint ensures that quality, safety, and reliability remain central to operations. The company focuses on bringing medicines of tomorrow to patients while fostering an inclusive environment where employees can thrive. By uniting a dynamic and agile workforce, Lonza maintains its position as a forward-focused partner in the pharmaceutical supply chain.
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