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We are seeking a detail-oriented and motivated Manufacturing Associate to support the production of therapeutic proteins (Active Pharmaceutical Ingredients – API) under current Good Manufacturing Practices (cGMP). This role involves executing process recipes, monitoring equipment and processes, and performing routine laboratory and sanitization tasks to ensure compliance and product quality.

Schedule: 7PM - 7AM rotating (3 days on, 3 days off, 2 days on, 2 days off)

Key Responsibilities:

+ Execute manufacturing process recipes and follow Standard Operating Procedures (SOPs) under cGMP conditions.

+ Monitor equipment and production processes, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations.

+ Perform basic laboratory tasks such as pH and conductivity measurements, sampling, and aseptic handling of materials.

+ Conduct routine sanitization of equipment and production areas to maintain a clean and compliant environment.

+ Accurately document production activities in both written and electronic formats in accordance with Good Documentation Practices (GDP).

+ Assist in material movements, including transferring raw materials and chemicals into, out of, and across production areas.

+ Develop a foundational understanding of cGMP compliance and aseptic techniques while training under close supervision.

Qualifications:

+ High school diploma or equivalent required; associate or bachelor’s degree in a scientific or technical field preferred.

+ Prior experience in a GMP-regulated manufacturing or laboratory environment is a plus.

+ Ability to follow detailed procedures and maintain accurate documentation.

+ Strong attention to detail and commitment to quality and safety.

+ Willingness to work in a cleanroom environment and adhere to strict hygiene protocols.

+ Good communication and teamwork skills.

Job Type & Location

This is a Contract position based out of Portsmouth, NH.

Pay and Benefits

The pay range for this position is $27.00 - $27.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Portsmouth,NH.

Application Deadline

This position is anticipated to close on Nov 21, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.