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Lonza

Biotechnologist I-Day Shift

US - Portsmouth, NH

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hirly's read of this role

Seniority
Mid level
Country
US
Work mode
On-site / unstated
First seen by hirly
4 Nov 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Manufacturing Associate II-Cell Therapy

Location: Portsmouth, NH, USA

Shift: 12 Hour Rotating/B Shift Days

Join Lonza's Cell Therapy Manufacturing team in Portsmouth, NH, where you will help deliver life-changing therapies to patients around the world. This is an exciting opportunity to develop your manufacturing expertise while working in a collaborative, GMP-regulated environment supporting both clinical and commercial operations.

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.

Opportunities for professional growth and technical development.

Exposure to advanced cell therapy manufacturing technologies.

The opportunity to contribute to therapies that improve patient lives.

What you will do

Perform manufacturing operations within cell therapy production areas while maintaining safety, quality, and compliance standards.

Support technical transfer and operational readiness activities for new customer programs.

Collaborate with Manufacturing, Quality, and cross-functional teams to deliver clinical and commercial products.

Train colleagues on new processes, equipment, and manufacturing systems.

Author, review, and maintain manufacturing documentation, including batch records, SOPs, and work instructions.

Support continuous improvement initiatives to enhance manufacturing processes and operational performance.

Ensure all activities are performed in compliance with GMP, EHS, and site procedures.

What we are looking for

High school diploma or equivalent required; bachelor's degree in biology or a related life sciences field preferred.

Experience in biotechnology, pharmaceutical manufacturing, cell therapy, or a related industry.

Knowledge of GMP principles and regulated manufacturing environments preferred.

Experience working in a cleanroom environment preferred.

Strong communication, collaboration, and organizational skills.

Ability to follow detailed procedures and manage multiple priorities in a fast-paced environment.

Commitment to quality, safety, continuous improvement, and teamwork.

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.

Original posting on Lonza's site ↗

Listed on hirly, a job board. hirly is not the employer: Lonza is hiring for this role.

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