Biotechnologist I (Days - B Shift)

Lonza•Portsmouth, NH

17d•Onsite

About The Position

We are seeking motivated individuals to join our rotational day shift (7 AM – 7 PM) in Portsmouth, NH, to help manufacture essential medicines. In this role, you will operate production equipment and perform foundational lab work while maintaining a clean, compliant facility. If you are a reliable professional looking to make a meaningful difference in the life sciences industry, we look forward to meeting you. Schedule: Shift: Rotational Day Shift (7:00 AM – 7:00 PM) Pattern: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeating cycle) 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 Medical, dental and vision insurance, as well as PTO and more Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits. What you’ll do: Production Operations: Set up, operate, and monitor core production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations. Basic Lab Work & Material Handling: Perform basic laboratory tasks, such as monitoring pH, conductivity, and product sampling, and accurately transfer raw materials and chemicals across production areas. Documentation & Compliance: Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs). Facility & Equipment Readiness: Maintain the cleanliness and organization of facilities and equipment, executing routine sanitization tasks and supporting 6S programs. Training & Development: Attain and maintain qualifications for all assigned tasks, actively keeping individual training plans up to date. Team & Administrative Support: Participate in essential administrative duties, including shift exchanges, meetings, email

Requirements

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

Nice To Haves

Prior experience in a GMP, biotech, or pharmaceutical environment is beneficial but not required.

Responsibilities

Set up, operate, and monitor core production equipment and processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.
Perform basic laboratory tasks, such as monitoring pH, conductivity, and product sampling, and accurately transfer raw materials and chemicals across production areas.
Accurately document all production activities in accordance with Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDPs).
Maintain the cleanliness and organization of facilities and equipment, executing routine sanitization tasks and supporting 6S programs.
Attain and maintain qualifications for all assigned tasks, actively keeping individual training plans up to date.
Participate in essential administrative duties, including shift exchanges, meetings, email