Biotechnologist Associate

Sunrise Systems, Inc.; Portsmouth (NH); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Biotechnologist Associate to join their team in Portsmouth. This exciting role involves manufacturing therapeutic proteins under strict cGMP conditions, ensuring compliance with industry standards. As part of a dynamic team, you will execute process recipes, monitor production, and maintain a clean room environment. Ideal candidates will have a scientific background and a passion for precision in manufacturing. This is a fantastic opportunity to grow in a supportive environment while contributing to innovative biotechnological advancements.

Qualifications

• Basic understanding of cGMP compliance and aseptic techniques.
• Experience in manufacturing or related fields is preferred.

Responsibilities

• Manufacturing therapeutic proteins under cGMP conditions.
• Monitor equipment and processes while following SOPs.

Skills

Manufacturing Experience

Basic Laboratory Skills

cGMP Compliance

Computer Skills

Mechanical Aptitude

Education

Scientific Degree

Tools

Clean-in-place (CIP) Systems

Steam-in-place (SIP) Systems

Job description

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Duration: 12 months Contract (Possible extension based on work performance)

Location: Portsmouth, NH 03801

Onsite/Hybrid: Onsite

Work Schedule: 12 HOUR SHIFTS - NIGHTS 7PM-7AM

Job Description:

The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. 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.

• 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 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. Must be willing to gown and work in a "clean room" environment.
• Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
• Perform other duties as assigned.

Candidates with the following backgrounds have had success in manufacturing at Client combined with scientific degree, manufacturing experience or courses/interests in science:

• Food service
• Cooks (can follow recipes)
• Pharmacy techs
• Mechanical aptitude
• Robotics
• Computer skills (this is increasingly important as our suites are more automated)
• EMTs
• Anything involving following SOPs, guidelines, industry regulations
• Security guards
• Nurses/nurse aides

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

Industries

• IT Services and IT Consulting

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Biotechnologist Associate - Manufacturing

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