Lonza
Biotechnologist I
United States · Work style not stated · Full time
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About the role
Description from the employer’s posting. Check the employer’s page for the current version.
- EmployerLonza
- LocationUnited States
- Work styleWork style not stated
- Employment typeFull time
- Employer posted
JobTitle: Biotechnologist I
Location: Portsmouth, NH, (On-site)
We are seeking a Manufacturing Associate I to join our Cell Therapy manufacturing team in Portsmouth, NH. In this entry-level role, you will help support manufacturing operations in a safe, compliant, and controlled environment. You will work alongside experienced colleagues to support production activities, technical transfers, equipment readiness, training activities, and continuous improvement initiatives. Become part of a talented team of people working together to help improve lives around the world.
This role follows a 12-hour day shift schedule from 7:00 AM to 7:00 PM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).
What you will get
Competitive pay and performance-based compensation
Medical, dental, and vision insurance
Show full description
Opportunities for career growth and development
Hands-on training and skill-building
Exposure to advanced Cell Therapy manufacturing technologies
The opportunity to help bring life-changing therapies to patients
What you will do
Support manufacturing operations in compliance with safety, quality, and cGMP requirements
Perform cleaning activities and help ensure manufacturing spaces are inspection-ready
Complete training in safety, gowning, material movement, environmental monitoring, and manufacturing processes
Support technical transfer activities, including training runs, engineering runs, and process readiness activities
Assist with the creation, review, and updating of manufacturing documentation
Learn and support customer manufacturing processes transferred into the Portsmouth facility
Collaborate with Manufacturing, Quality, MSAT, and other teams to support project milestones
What we are looking for
Experience in a GMP, biotechnology, pharmaceutical, or manufacturing environment is preferred
Basic understanding of cGMP principles and cleanroom operations preferred
Strong communication and teamwork skills
Ability to follow detailed procedures and work in a fast-paced environment
Basic computer skills and familiarity with Microsoft Office applications
Willingness to learn new processes, equipment, and systems
Commitment to safety, quality, and continuous improvement
Curiosity with a willingness to learn and understand processes
Associate or bachelor's degree in a scientific or technical field preferred
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.
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At a glance
- Employment typeFull time
- Employer posted
- Added to ROLIVA
- Last checked