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Lonza in Portsmouth, NH seeks a Manufacturing Supervisor for Cell Therapy to lead nightly manufacturing operations, plan schedules, review records, and coach operators in a cGMP environment. You will partner with cross-functional teams to resolve obstacles and drive continuous improvement while ensuring safety and quality.
The role requires an AS/BS in science, 5–10 years GMP/manufacturing experience, and up to 50 lbs lifting, with 1–4 years supervisory experience preferred and on-site night
United States, Portsmouth (New Hampshire)
Location: Portsmouth, NH (On-site)
Join a collaborative team where you’ll help manufacture life‑changing therapies. You’ll guide operations in a cGMP environment and contribute directly to delivering high‑quality products to patients and efficient production activities throughout the night schedule.
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.
Reference: R79102