Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is dedicated people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want you to be part of!
We are seeking a motivated and detail-oriented Biotechnologist I to join our production team in Portsmouth, NH. This full-time, on-site role supports day shift operations (7 AM – 7 PM) on a rotational schedule. The Biotechnologist I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP). Working under close supervision, associates will execute process recipes, follow written procedures (SOPs), monitor equipment and processes, and perform basic laboratory tasks such as pH and conductivity testing and sampling.
This role also includes routine sanitization tasks to maintain facility and equipment standards, and requires the demonstration of aseptic technique in handling products and materials. The ideal candidate will be eager to learn, comfortable asking questions, and committed to maintaining compliance with cGMP and GDP standards.
Schedule
Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat)
Day Shift: 7:00 AM – 7:00 PM
Weekend shifts include additional pay.
Key Responsibilities
Set up, operate, and monitor production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.
Document production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).
Attain and maintain qualifications for assigned tasks and keep individual training plans up to date.
Perform basic laboratory tasks such as monitoring pH, conductivity, and testing product samples.
Transfer raw materials and chemicals across production areas.
Maintain cleanliness and organization of facilities and equipment; support 6S programs.
Participate in administrative tasks including shift exchanges, meetings, emails, and project involvement.
Perform other duties as assigned.
Required Qualifications
High school diploma or equivalent.
Experience in GMP, biotech, or pharmaceutical environments is a plus but not required.
Preferred Skills
Strong attention to detail.
Comfortable asking questions and following Standard Operating Procedures (SOPs).
Reporting Structure
Reports to a Shift Supervisor.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference!
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.