Biotechnologist II - Cell Therapy (Nights)

LonzaPortsmouth, NH
Onsite

About The Position

We are seeking a motivated and detail-oriented individual to join our manufacturing team in Portsmouth, NH, as a Biotechnologist II. This intermediate-level role is responsible for the hands-on cGMP production of patient-specific treatments within our Cell Therapy asset. Operating under general supervision, you will maintain a safe, controlled environment, execute complex processing recipes, and serve as a reliable floor resource for core production stages.

Requirements

  • 1–3 years of related biological manufacturing experience with a degree.
  • Prior experience in a cleanroom or automated processing environment is required.
  • Expert proficiency in aseptic technique, strong familiarity with sterile gowning procedures, and a proven track record of executing tasks under strict Standard Operating Procedures (SOPs).
  • Ability to think quickly, draw accurate conclusions, and handle fast-paced production campaigns effectively within a close-knit team setting.
  • High School Diploma or equivalent is required.
  • Ability to sit or stand for extended periods, perform precise fine motor movements, comfortably handle continuous sterile gowning, and occasionally lift up to 50 lbs.

Nice To Haves

  • An Associate's or Bachelor's Degree in a life sciences discipline (Biology, Biotechnology, Biochemistry, etc.) is preferred.

Responsibilities

  • Run core manufacturing unit operations under aseptic conditions to support clinical and commercial timelines.
  • Execute daily tasks in strict accordance with cGMP regulations, adhering to rigorous hygienic principles and mandatory Grade B cleanroom gowning requirements.
  • Participate alongside customer SMEs in tech transfer activities, providing operational input into material requirements, water runs, and engineering runs.
  • Author, review, and execute manufacturing documentation (electronic batch records, SOPs, and logbooks) for completeness, clarity, and strict GDP compliance.
  • Manage routine suite readiness tasks, including cleaning, facility sanitization, equipment setup, and 6S tracking to prevent contamination risks.
  • Provide hands-on training and guidance to junior colleagues during their onboarding period, acting as a reliable, safety-conscious example on the floor.
  • Coordinate with Quality Assurance, engineering, and material specialists to ensure milestones are met and process improvements are smoothly integrated.

Benefits

  • An agile career and dynamic working culture
  • An inclusive and ethical workplace
  • Specialized Cleanroom Expertise: Hone advanced aseptic techniques and Grade B cleanroom processing skills within a cutting-edge cell therapy asset.
  • Compensation programs that recognize high performance
  • Medical, dental and vision insurance, as well as PTO and more
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