Manufacturing Biotechnologist 1 - Day Shift

Creative Solutions Services, LLC; Portsmouth (NH); On-site; USD 32,000 - 41,000; Part time

Job summary

Creative Solutions Services, LLC is seeking a Manufacturing Biotechnologist I for a 6‑month, onsite assignment in Portsmouth, NH. The role focuses on manufacturing therapeutic proteins under cGMP with supervision and training on SOPs, process monitoring, and basic lab tasks.

Responsibilities include setting up equipment, monitoring production, and handling material movements while maintaining GMP/GDP documentation.

Qualifications

• Requires basic GMP understanding and willingness to train under supervision.
• Strong written and verbal communication skills are required.
• Ability to perform basic laboratory tasks and follow SOPs.

Responsibilities

• Set up, operate, and monitor production processes including CIP/SIP operations and document production per GMP/GDP.
• Attain qualification for all tasks and maintain training plan.
• Perform basic lab tasks such as monitoring pH and conductivity and testing samples.
• Move materials, transfer raw materials and chemicals between production areas.
• Maintain facility and equipment through routine cleaning and sanitization, support 6S.
• Attend shift exchanges, meetings, and email communications; participate in projects.
• Perform other duties as assigned.

Skills

Logic & decision making

Written & verbal communication

Job description

Manufacturing Biotechnologist 1 - Day Shift #26-01872

Up to $26.85 per hour Portsmouth, NH Onsite

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Job Description

Title: Manufacturing Biotechnologist 1 - Day Shift

Location: 101 International Drive, Portsmouth, NH

Contract: 6 Months - possibility for extension or FTE conversion

Pay Rate: $26.85 per hour + Benefits

Shift : Day Shift (6:00 AM - 6:30 PM)

Shift Details

This is a 12-hour Day Shift (6:00 AM - 6:30 PM) on a rotating schedule. Employees work Monday, Tuesday, Friday, Saturday, and Sunday one week, followed by Wednesday and Thursday the next week. Candidates must be comfortable with this alternating schedule and overnight hours.

JOB DESCRIPTION

The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

Roles and Responsibilities

• Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
• Attain qualification for all assigned tasks and maintain individual training plan.
• Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
• Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
• Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
• Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
• Perform other duties as assigned.

Skills

• Proven logic and decision making abilities, critical thinking skills
• Strong written and verbal communication skills are required

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