Manufacturing Biotechnologist 1

JobDiva, Inc.; Portsmouth (NH); On-site; USD 36,000 - 52,000; Full time

Job summary

Creative Solutions Services, LLC is seeking a Manufacturing Associate Level I in Portsmouth, NH. The role focuses on manufacturing therapeutic proteins under cGMP conditions, following SOPs, and maintaining equipment and documentation with basic lab tasks under supervision.

The position emphasizes aseptic technique, adherence to GMP/GDP, and routine sanitization, with responsibilities spanning production, documentation, and cross-functional collaboration.

Qualifications

• Proven logic and decision making abilities.
• Strong written and verbal communication skills.

Responsibilities

• Set up, operate equipment, and monitor production processes per GMP/GDP, with CIP/SIP as applicable.
• Attain qualification for all assigned tasks and maintain individual training plan.
• Perform basic laboratory 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.
• Administrative tasks – shift exchanges, meetings, emails; participate in projects.
• Perform other duties as assigned.

Skills

Critical thinking

Written communication

Verbal communication

Education

High School diploma or equivalent

Job description

Summary:

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.

Job Description (Key Accountabilities):

• 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.

Education:

• High School Diploma or Equivalent

Work Experience:

• Entry Level - 0-4 years.
• Proven logic and decision making abilities, critical thinking skills.
• Strong written and verbal communication skills are required.