GMP QC Analyst - Cell & Gene Therapy Operations

Vertex Pharmaceuticals

Boston (MA)

On-site

USD 52,000 - 62,000

Full time

14 days+

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Job summary

Vertex Pharmaceuticals in Boston is seeking a QC Operations Analyst to support QC operations within a fast-paced GMP setting in the Cell and Gene Therapy Department. You will collaborate with facilities, validation, metrology and vendors to keep lab activities on track.

The ideal candidate holds a Bachelor's in Chemical Engineering or a related field, with 0–2 years GMP lab experience. Proficiency in Excel and Word, plus SOP development and instrument maintenance, are expected.

Qualifications

  • Bachelor's degree in Chemical Engineering, scientific field or equivalent.
  • 0-2 years GMP lab experience preferred.
  • Equivalency may be considered with related education and experience.

Responsibilities

  • Work cross functionally with internal and external teams to minimize lab interruptions.
  • Identify and create processes to ensure success within the QC lab.
  • Manage sample, reagent and chemical lifecycle.
  • Establish and update SOPs in line with GMP guidelines.
  • Set up and maintain instrumentation with cross functional teams.
  • Maintain QC equipment and perform calibration per SOP.
  • Communicate project status to the project leader.
  • Perform assignments accurately, timely and safely.
  • Shift work applies.
  • Able to perform aseptic gowning.

Skills

GMP experience
Excel
Word
Problem solving
Communication
Time management
Teamwork

Education

Bachelor's degree in Chemical Engineering or related field

Tools

LIMS

Job description

Vertex Pharmaceuticals in Boston is seeking a QC Operations Analyst to support QC operations within a fast-paced GMP setting in the Cell and Gene Therapy Department. You will collaborate with facilities, validation, metrology and vendors to keep lab activities on track.

The ideal candidate holds a Bachelor's in Chemical Engineering or a related field, with 0–2 years GMP lab experience. Proficiency in Excel and Word, plus SOP development and instrument maintenance, are expected.

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