Biotechnologist I
Lonza
Summary
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.
Job description
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 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
Requirements
- 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
Benefits
- Competitive pay
- Performance-based compensation
- Medical, Dental & Vision
- Career growth and development
- Hands-on training
- Exposure to advanced technologies
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.