Job Description

Responsibilities

  • Prepare qualification protocols for Autoclaves, Sterilizers, Chambers, Freezers and Warehouses etc.
  • Perform testing and write reports for executed protocols
  • Conduct statistical analysis of validation test results and advice client
  • Investigation/ troubleshooting of validation problems
  • Meet project deadlines

Requirements

  • Bachelor's Degree in Science, Food Tech, Chemical, Biomedical Engineering or Equivalent.
  • 2 years experience in pharmaceutical manufacturing or quality department a real plus.
  • Entry level with no to little experience are also welcome to apply.
  • Good positive attitude and ability to learn fast.
  • Capable of developing alternative solutions to issues at hand.
  • Knowledge of cGMP and FDA/EU, PDA, ISPE, WHO guidelines.
  • Knowledge of acceptance criteria, readily identify discrepancies.
  • Good in technical writing, communication, a...

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