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Job Description

Title: Cell Processing Specialist
Job ID: AW752116718

Position Accountabilities:
  • Execute unit operations for manufacturing of patient therapies according to standard operating procedures and cGMP, regulatory and safety requirements. Duties include basic cell culture as well as specialized techniques for cell selection, activation, transduction, and purification
  • Perform operations in a cleanroom environment, using proper controls to assure aseptic processing: includes gowning, cleaning, and isolation procedures
  • Perform supporting operations as needed including preparation of consumables, media blending, cleaning, and environmental monitoring
  • Complete all daily manufacturing tasks following standard operating procedures and batch document instructions, completing forms, reports, logs and records of equipment, and batches as required
  • Ensure all training assignments are complete and up to date, to maintain necessary technical skills and knowledge
  • Ensure processing equipment and required materials are available, maintained, and qualified as required for the different manufacturing activities
  • Support investigations in manufacturing and technical deviations
  • Actively participate in problem identification, problem solving, and change initiatives in cooperation with other teams and functions
  • Collaborate with process development scientist to get trained and transfer new processes into cGMP manufacturing
Education, Experience and Skills:
  • Associates degree in biotechnology, chemistry, pharmacy, engineering or related pharmaceutical science and 4+ years relevant cGMP manufacturing experience
  • Bachelors degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 2+ years relevant cGMP manufacturing experience
  • Masters degree in chemistry, biology, pharmacy, engineering or related pharmaceutical science; 0+ years relevant cGMP manufacturing experience
  • Previous hands-on experience in a cGMP or clinically regulated environment is critical
  • Knowledge of aseptic processing in ISO 5 biosafety cabinets strongly preferred
  • Manufacturing experience in biopharmaceutical operations, preferably involving cell cultures or Regenerative Medicines.
  • Experience with culture and handling of human primary cells including T-cells
For information about TEEMA and to consider other career opportunities, please visit our website at www.teemagroup.com

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* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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