2nd shift Quality Control Specialist (contract) 28670

Vertex PharmaceuticalsBoston, MA
$40 - $50

About The Position

The Vertex Cell and Gene Therapy (VCGT) Type 1 Diabetes (T1D) Quality Control (QC) team is responsible for the testing of samples and associated workflows within our stem-cell based T1D program. VCGT T1D QC carries out all activities under Good Manufacturing Practices (GMP) guidelines. The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation, testing and reporting of in-process, release and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values. Shift: Sunday - Wednesday 12:30pm-11:00pm

Requirements

  • A minimum of a Bachelor's degree in Sciences is required.
  • 4 + years of experience in the GMP pharmaceutical/biopharmaceutical industry
  • Performs tasks with strict adherence to cGMP and cGDP principles.
  • Has an understanding of basic laboratory equipment and practices.
  • Is proficient in the use of spreadsheets and word processing software.
  • Is dependable and able to work well within a team.
  • Is interested in learning new things. Open to change.
  • Is optimistic and displays a positive attitude even during periods of adversity.
  • Shows initiative; acts independently with management approval.
  • Possesses a high attention to detail.

Responsibilities

  • Typical test methods performed include flow cytometry, qPCR (MycoTOOL), ELISA, cell counts, sterility (BACT), Gram stain and endotoxin (LAL) testing.
  • Performs technical reviews of raw data.
  • Records test results and maintains raw data and accurate laboratory records.
  • Performs general lab and equipment maintenance duties.
  • Performs other duties as assigned.
  • Weekend shift work: Typical workweek is a 4 day week, 10 hours a day, Sunday to Wednesday 12:30 PM – 11:00 PM.
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