Job Title: Manufacturing Associate III
Location: Portsmouth, NH, (On-site)
As a Manufacturing Associate III at our Portsmouth site, you will play a key role in upstream production of therapeutic proteins that support patients worldwide. You will operate manufacturing equipment, execute complex processes, and ensure all work meets cGMP and safety standards. This is an onsite role requiring hands-on work and close collaboration. You will also support troubleshooting, lead by example within the team, and contribute to continuous improvement initiatives.
This role follows a 12-hour day shift schedule from 7:00 AM to 7:00 PM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).
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
Opportunities to grow and develop your career
A collaborative and team-focused environment
What you will do
Set up, operate, and monitor manufacturing equipment, including CIP and SIP processes
Execute production processes following SOPs, cGMP, and GDP requirements
Perform advanced laboratory tasks such as sampling, pH, and conductivity testing
Troubleshoot routine and non-routine equipment and process issues
Review batch records, logbooks, and support deviation initiation
Train and support other associates on manufacturing tasks and process knowledge
Perform material movements and maintain equipment through cleaning and sanitization
What we are looking for
3+ years of upstream bioprocessing experience required; 5+ years in the biotech industry preferred
Experience in GMP manufacturing or a regulated biopharmaceutical environment
Strong understanding of cGMP, documentation practices, and process flow
Ability to troubleshoot equipment and support investigations
Strong communication skills, including technical writing
Attention to detail with strong problem-solving and decision-making skills
High school diploma or equivalent required; Associate’s or Bachelor’s degree in a science-related field preferred
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.
Skills Required
- 3+ years of upstream bioprocessing experience
- Experience in GMP manufacturing or regulated biopharmaceutical environment
- Strong understanding of cGMP, documentation practices, and process flow
- Ability to troubleshoot equipment and support investigations
- Strong communication skills, including technical writing
- Attention to detail with strong problem-solving and decision-making skills
- High school diploma or equivalent
- 5+ years in the biotech industry
- Associate's or Bachelor's degree in a science-related field
What We Do
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.
