Biotechnologist II (Days - B Shift)

Biotechnologist II (Day Shift)

Location: Portsmouth, NH, USA. The actual location of this job is in Portsmouth, NH, USA.

Take the next step in your manufacturing career as a Biotechnologist II on our Portsmouth day shift. Working from 7 AM - 7 PM, you will play a key role in producing life-saving therapeutic proteins while expanding your technical expertise in troubleshooting and quality systems.

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.

See what a role at Lonza (Portsmouth, NH) looks like-watch this short video!

What you will get

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Compensation programs that recognize high performance.

• Medical, dental and vision insurance

• Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits

What you will do

• Set up, operate equipment, and monitor production processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

• Report production in written and electronic documents in accordance with GMPs and GDPs, ensuring accuracy in all documentation reviews.

• Troubleshoot routine equipment and process issues as appropriate to maintain production flow and batch integrity.

• Demonstrate proficiency in laboratory tasks such as monitoring pH, conductivity, and product sampling, with the opportunity to train Level I Associates on these tasks.

• Perform material movements, including the transfer of raw materials and chemicals into, out of, and across production areas.

• Maintain facility and equipment through routine cleaning, sanitization, and active support of 6S programs.

• Attain and maintain qualifications for all assigned tasks while participating in administrative duties like shift exchanges, meetings, and special projects.

What we are looking for

• Education: High School Diploma or Equivalent is required; an Associate's or Bachelor's degree in a Science-related discipline is preferred.

• Experience: 1-3 years of experience in a cGMP manufacturing environment, showing a clear progression in technical responsibility.

• Technical Skills: Strong foundational knowledge of aseptic processing and the ability to independently perform analytical lab tests.

• Compliance: A solid understanding of cGMP regulations and a commitment to meticulous documentation.

• Problem Solving: Emerging ability to troubleshoot equipment and a proactive approach to identifying process improvements.

• Communication: Effective verbal and written communication skills for shift handovers and technical documentation review.

• Schedule: Ability to work the 7 AM - 7 PM rotational day shift in a fast-paced production environment.

About Lonza

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. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

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. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

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