Manufacturing Associate Level 1

Lonza; Portsmouth (NH); On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Career growth

Team collaboration

Competitive compensation

Job summary

Lonza in Portsmouth, NH, is seeking a Manufacturing Associate III to join our onsite team. You will set up, operate, and monitor upstream production equipment and perform advanced laboratory tasks while ensuring adherence to cGMP and safety standards.

The role follows a 12-hour night shift (7:00 PM–7:00 AM) on a rotating two-on, two-off, three-on, two-off cycle. You will train others, support investigations, and contribute to continuous improvement within a collaborative, on‑site environment.

Qualifications

• 3+ years upstream bioprocessing experience required.
• 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; Associate's or Bachelor's degree in a science-related field preferred.

Responsibilities

• 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.

Skills

Upstream bioprocessing

GMP manufacturing

cGMP documentation

Equipment troubleshooting

Technical writing

Attention to detail

Education

High school diploma or equivalent

Science-related bachelor’s degree preferred

Job description

United States, Portsmouth (New Hampshire)

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 PM to 7:00 AM 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.