Biotechnologist I (Nights – A Shift)

Lonza•Portsmouth, NH

5d•Onsite

About The Position

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're looking for a motivated Biotechnologist I to join our full-time, on-site production team in Portsmouth, NH, working a rotational night shift (7 PM – 7 AM). This role is responsible for the cGMP manufacture of therapeutic proteins (API), requiring the execution of process recipes and adherence to written procedures under close supervision. Key duties include monitoring equipment, performing basic lab tasks like pH/conductivity testing and sampling, and executing routine sanitization to maintain the facility. The ideal candidate must be eager to learn, demonstrate aseptic technique, and be committed to maintaining cGMP and GDP compliance. Find out more about what a role at Lonza in Portsmouth, NH could look like for you, by watching this short video. Schedule: Rotational: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeat) Night Shift: 7:00 PM – 7:00 AM Nights and Weekend shifts include additional pay. What will you get? An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance Comprehensive benefits including Medical, Dental, Vision, PTO, and more The full list of our global benefits can also be found at: https://www.lonza.com/careers/benefits .

Requirements

Education: High school diploma or equivalent is required, AS/BS in Science-related fields is preferred
Compliance & Process: Must be comfortable asking questions and strictly following Standard Operating Procedures (SOPs).
Core Skills: Strong attention to detail is essential for accurate execution of tasks.

Nice To Haves

Experience (A Plus): Prior experience in a GMP, biotech, or pharmaceutical environment is beneficial but not required.

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.