Quality Control Specialist II

1 day ago


Philadelphia, Pennsylvania, United States Iovance Biotherapeutics Inc Full time
Job Summary

We are seeking a highly skilled Quality Control Analyst II to support quality control testing operations at our Cell Therapy Center. The successful candidate will be responsible for performing daily cGMP quality control laboratory microbiological testing activities, environmental monitoring, and data analysis.

Key Responsibilities
  • Perform daily cGMP quality control laboratory microbiological testing activities, including bioburden, endotoxin, gram stain, and sterility techniques.
  • Conduct environmental monitoring of cleanroom areas as scheduled.
  • Perform data analysis and result reporting of microbiology assays to support product lot release.
  • Support thorough cGMP investigations for out-of-specification test results.
  • Perform environmental monitoring data trending.
  • Support technical problem-solving and product stability programs.
Requirements
  • Bachelor's degree in a relevant discipline (biological sciences or equivalent).
  • Minimum 3 years' experience in the pharmaceutical industry within a Quality Control role.
  • Excellent communication and interpersonal skills.
  • Ability to work in a team environment and prioritize tasks effectively.
  • Strong attention to detail and analytical skills.
Work Environment

This position will work in both an office and a manufacturing lab setting. The successful candidate must be able to work in a lab setting with various chemical/biochemical exposures, including latex and bleach.

Iovance Biotherapeutics Inc is an equal-opportunity employer committed to diversity and inclusion. We welcome applications from qualified candidates who share our values and are passionate about delivering high-quality results.



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