Biotechnologist III; Nights - B Shift

Biotechnologist III

Location:

Portsmouth, NH, USA.

We are seeking a fully proficient Biotechnologist III to join our full‑time, on‑site production team in Portsmouth, NH, working a rotational night shift (7 PM – 7 AM). This intermediate‑level role is responsible for the cGMP manufacture of therapeutic proteins (API), focusing heavily on upstream operations involving 2K bioreactors. You will independently execute process recipes, monitor equipment, and demonstrate significant knowledge of upstream process flow to troubleshoot routine and non‑routine events, initiate deviations, and train other operators on specialized techniques.

• Shift: Rotational Night Shift (7:00 PM – 7:00 AM)
• Pattern: 2 on, 2 off, 3 on, 2 off, 2 on, 3 off (repeating cycle)
• Nights and weekend shifts include additional pay.

• 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:

• Upstream Operations & Troubleshooting:
  Set up, operate, and monitor 2K bioreactors and core production equipment (including CIP/SIP), and troubleshoot routine and non‑routine equipment events within the upstream suite.
• Specialized Lab Work & Process Flow:
  Independently perform specialized laboratory tasks (e.g., pH, conductivity, product sampling, media preparation) and demonstrate an in‑depth understanding of upstream process flow to make experience‑based decisions.
• Documentation & Quality Review:
  Accurately report production activities, review batch records and logbooks, and initiate deviations in accordance with GMPs and GDPs, utilizing technical writing skills.
• Training & Technical Mentorship:
  Act as a qualified trainer, mentoring other operators on assigned tasks and the scientific theory behind upstream production activities (e.g., bioreactor inoculation, large‑scale cell culture).
• Material Handling & Facility Readiness:
  Perform all material movements, transferring raw materials and chemicals across production areas. Maintain facility and equipment through routine cleaning, sanitization, and 6S programs.
• Team & Administrative Support:
  Participate in administrative duties, including shift exchanges, meetings, and project involvement, supporting overall team compliance and effectiveness.

• Education:
  
  High school diploma or equivalent is required. An AS/BS in a science‑related field is preferred.
• Experience & Proficiency: 2‑4 years of experience in upstream (fermentation/cell culture) large‑scale GMP/biotech manufacturing, demonstrating full proficiency in bioreactor operations.
• Compliance & Independence:
  Demonstrated ability to work independently and troubleshoot issues, possessing a significant, in‑depth understanding of cGMP compliance.
• Core
  
  Skills:
  
  Strong attention to detail, proficiency in technical writing, and effective communication skills for training and collaboration.

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. 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.

Ready to shape the future of life sciences? Apply now. Reference: R71537