Manufacturing Associate I - GMP Training & Growth (On-site)

Lonza

Portsmouth (NH)

On-site

Confidential

Full time

14 days+
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Benefits offered by this job

Competitive pay and performance-based
Medical, dental, and vision insurance
A supportive and inclusive work
Opportunities for career growth and
Hands-on training and skill-building
A dynamic and team-focused workplace

Job summary

Lonza in Portsmouth, NH is seeking a Manufacturing Associate I to help produce life-saving therapeutic proteins in a regulated environment. The role involves 12-hour day shifts on a rotating schedule (7:00 AM–7:00 PM) and requires strong attention to detail and teamwork.

You will perform GMP-driven tasks, support cleaning (CIP/SIP), and contribute to continuous improvement. Applicants should have a high school diploma or equivalent, with science-based degree preferred.

Qualifications

  • High school diploma or equivalent required; science degree preferred.
  • Basic lab tasks and GMP procedures experience.
  • Willingness to learn and follow regulated processes.
  • Strong attention to detail and clear communication.
  • Ability to work in a hands-on production environment.

Responsibilities

  • Operate and monitor manufacturing equipment following GMP procedures.
  • Set up and support cleaning processes, including CIP and SIP.
  • Perform basic lab tasks such as monitoring pH, conductivity, and testing samples.
  • Handle and move materials across production areas safely.
  • Complete production and documentation records accurately.
  • Maintain clean, safe, and organized workspaces.
  • Support team activities, meetings, and continuous improvement efforts.

Skills

Attention to detail
Problem-solving
Communication
Process adherence
Teamwork
Hands-on work
Curiosity

Education

High school diploma or equivalent
Associate's or Bachelor's degree in science (preferred)

Job description

Lonza in Portsmouth, NH is seeking a Manufacturing Associate I to help produce life-saving therapeutic proteins in a regulated environment. The role involves 12-hour day shifts on a rotating schedule (7:00 AM–7:00 PM) and requires strong attention to detail and teamwork.

You will perform GMP-driven tasks, support cleaning (CIP/SIP), and contribute to continuous improvement. Applicants should have a high school diploma or equivalent, with science-based degree preferred.

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