Manufacturing Associate - Biotech

Job Title: Manufacturing Associate - Biotech
Location: 101 International Drive Portsmouth NH USA 03801
Duration: 12-month contract (Potential for extension or permanent hire)
Nights - 7PM - 7AM - rotating days - every other weekend.
Pay Rate: $27/hr (W2)
Benefits: Weekly pay, Medical, Dental, and Vision coverage.

Role Summary
The Manufacturing Associate supports the production of therapeutic protein active pharmaceutical ingredients (APIs) in a cGMP-regulated manufacturing environment. This role involves executing manufacturing processes by following approved SOPs and batch records, operating and monitoring production equipment, performing basic laboratory testing, and maintaining cleanroom and equipment standards. Associates work under close supervision while developing a strong foundation in aseptic technique, cGMP compliance, and manufacturing operations.

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Key Duties & Responsibilities

• Execute manufacturing process recipes and procedures in accordance with SOPs, batch records, cGMP, and GDP requirements.
• Set up, operate, and monitor production equipment, including Clean-In-Place (CIP) and Steam-In-Place (SIP) systems.
• Perform basic laboratory and in-process testing, including pH, conductivity, sampling, and product testing.
• Monitor equipment performance and process parameters; report deviations and production data accurately in written and electronic systems.
• Perform material movements, including transfer of raw materials, chemicals, and components across production areas.
• Maintain facility and equipment cleanliness through routine cleaning and sanitization; support 6S/lean manufacturing programs.
• Gown and work in controlled cleanroom environments, adhering to aseptic techniques at all times.
• Complete administrative tasks such as shift handoffs, meetings, documentation, emails, and participation in continuous improvement projects.
• Attain qualification for assigned tasks and maintain an individual training plan.
• Perform additional duties as assigned to support manufacturing operations.

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Requirements & Preferred Background

• Ability to follow detailed written procedures, recipes, and regulatory guidelines with accuracy and consistency.
• Basic understanding or willingness to learn cGMP, SOPs, GDP, and aseptic processing.
• Mechanical aptitude and comfort working with automated or semi-automated equipment.
• Strong attention to detail, documentation accuracy, and safety compliance.
• Willingness to gown and work in cleanroom environments.
• Computer proficiency for electronic documentation and automated manufacturing systems.