3rd Shift - Quality Control Sr. Associate/Sr. Specialist (contract) 29622

Vertex PharmaceuticalsBoston, MA
$42 - $67Onsite

About The Position

The Vertex Cell and Gene Therapy (C>) Quality Control (QC) team is responsible for the routine testing of samples and associated workflows for our internally manufactured stem-cell based T1D and genetically modified Casgevy programs. C> QC carries out all activities under Good Manufacturing Practices (GMP) guidelines. The 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.

Requirements

  • A minimum of a Bachelor's degree in related field of science is required (Biology, Biochemistry, etc).
  • Sr. Associate: 2-4 years, Specialist: 4-6, Sr. Specialist 6-8 years of experience in the GMP pharmaceutical/biopharmaceutical industry
  • Demonstrated laboratory experience in multiple methodologies listed above
  • Extensive experience working with flow cytometry
  • Proficient in the use of spreadsheets and word processing software.
  • Experience with electronic lab notebook (LIMS), and demonstrated ability to work with electronic instrument software

Nice To Haves

  • Has an understanding of basic laboratory equipment and practices.
  • 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

  • Performs technical reviews of raw data.
  • Records test results and maintain raw data and accurate laboratory records on paper and in electronic systems.
  • Performs general lab and equipment maintenance duties.
  • Performs other duties as assigned.
  • Troubleshooting analytical methods and participating in Quality Events (Deviations, OOS).

Benefits

  • medical benefits
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service