Day & Night Shift: Biotechnologist Associate

Sunrise Systems, Inc.; Portsmouth (NH); On-site; USD 35,000 - 60,000; Full time

Job summary

An established industry player is seeking a Manufacturing Associate to join their team in a cleanroom environment. This role involves the manufacturing of therapeutic proteins under stringent cGMP conditions, where you will execute process recipes, monitor equipment, and perform essential laboratory tasks. Ideal candidates will have a strong background in science and experience in sterile settings, showcasing their critical thinking and communication skills. Join this innovative firm and contribute to advancements in the Cell and Gene Therapy field, while working in a collaborative and supportive environment.

Qualifications

• High School Diploma required; AS/BS in Science preferred.
• Experience in cleanroom or laboratory settings preferred.

Responsibilities

• Manufacture therapeutic proteins under cGMP conditions.
• Operate equipment and monitor production processes.
• Maintain facility and equipment through cleaning and sanitization.

Skills

Aseptic Techniques

Critical Thinking

Written Communication

Verbal Communication

Documentation Procedures

Education

High School Diploma

AS/BS in Science

Job description

Duration: 12 monthsContract (Possible extension based on work performance)

Location: Portsmouth, NH 03801

Onsite/Hybrid: Onsite

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

NIGHTS-12 HOUR SHIFTS -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.
• High School Diploma or equivalent experience minimum with an AS/BS preferred
• Preferred area of study: Science related field, degrees in Genetics are relevant.
• Prior work experience in a cleanroom, laboratory, or another sterile setting is preferred.
• Prior experience with Aseptic Techniques and gowning procedures is preferred.
• Working experience in manufacturing; cGMP setting preferred. The ideal candidate will have experience within the Cell and Gene Therapy field.
• Able to follow documentation procedures for day-to-day tasks in a regulated industry
• Proven logic and decision-making abilities, critical thinking skills.
• Strong written and verbal communication skills.

Skills