Cell Therapies Development Specialist

1 week ago

Singapore beBeeBiotechnologist Full time $80,000 - $120,000
Cell Therapy Biotechnologist

A Cell Therapy Biotechnologist is responsible for the manufacture of therapeutic cell products under strict quality control guidelines.

Working closely with a team of technical and supervisor colleagues, you will execute production activities through to filling of final dose product within a classified clean room environment.

The goal of this position is to develop expert technical knowledge and flawless execution of the Cell Therapy production process.

Production activities occur in the classified production suite which requires compliance with clean room standards.

  • Removal of jewelry/make-up
  • Donning of over suits/coveralls
  • Safety shoes, shoe covers/booties
  • Hair cover
  • Gloves
  • Safety glasses/shield

This role is ideal for individuals with an interest in Cell Therapy production wanting to develop their production career in a different technical/scientific area.

Thorough training and continual assessment will be provided. After training, successful applicants would be expected to join day, weekend, and public holiday rotation shifts (12 hours).

Key Responsibilities
  1. Comply with site/department EHS standards (policies, rules, and regulations)
  2. Attain a thorough understanding of the principles of CGMP compliance and clean room practices
  3. Contribute to maintenance of 'in-operation' production facilities and equipment

Responsibilities include:

  • Medium preparation followed by aseptic filtration into sterile containers
  • Revival and culturing of anchorage-dependent cell lines in static flasks and cell factories
  • Harvest and concentration of cell factory-generated cell cultures using tangential flow filtration and/or centrifugation
  • Final formulation and filling of vials. Visual inspection and cryopreservation
  • Participation in aseptic process simulations
  • Accurate and thorough completion of batch record documentation
  • Environmental monitoring (viable particulates, non-viable particulates, surface, and operator)
Requirements
  • Degree/Diploma/NITEC in a related Science/Engineering discipline
  • Individuals without prior experience in biopharmaceutical manufacturing are encouraged to apply as training will be provided
  • Knowledge of cGMP applications
  • Knowledge of cell culture and aseptic processing within a classified environment
  • Strong team-oriented work ethic
  • Positive team-oriented attitude
  • Strong communication and interpersonal skills
  • Willingness to perform rotating 12-hour shift patterns

Ability to perform physical activities in a clean room environment, including standing, manual work (>60%), and carrying items up to 12 kg.

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