TalentBurst, an Inc 5000 company
Biotechnologist Associate
TalentBurst, an Inc 5000 company, Portsmouth, New Hampshire, United States, 00215
Biotechnologist Associate
Location: Portsmouth, NH (03801) Duration: 11+ months Shift: 12‑hour shifts (7AM‑7PM) 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 GMPs and GDPs, review documentation as appropriate. 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. Perform material movements: transfer raw materials and chemicals into, out of, and across production areas. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs, and be willing to gown and work in a clean‑room environment. Attend shift exchange meetings, send/receive emails, participate in projects. Perform other duties as assigned. Qualifications
High School Diploma or equivalent; AS/BS preferred. Preferred area of study: science‑related field; genetics degrees are relevant. Prior work experience in a cleanroom, laboratory, or sterile setting is preferred. Prior experience with aseptic techniques and gowning procedures is preferred. Working experience in manufacturing within a cGMP setting preferred; experience within the Cell and Gene Therapy field ideal. Ability 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.
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Location: Portsmouth, NH (03801) Duration: 11+ months Shift: 12‑hour shifts (7AM‑7PM) 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 GMPs and GDPs, review documentation as appropriate. 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. Perform material movements: transfer raw materials and chemicals into, out of, and across production areas. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs, and be willing to gown and work in a clean‑room environment. Attend shift exchange meetings, send/receive emails, participate in projects. Perform other duties as assigned. Qualifications
High School Diploma or equivalent; AS/BS preferred. Preferred area of study: science‑related field; genetics degrees are relevant. Prior work experience in a cleanroom, laboratory, or sterile setting is preferred. Prior experience with aseptic techniques and gowning procedures is preferred. Working experience in manufacturing within a cGMP setting preferred; experience within the Cell and Gene Therapy field ideal. Ability 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.
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