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Esco Lifesciences Group
www.escolifesciences.com

VALIDATION SPECIALIST

Looking for
S1

Hi Esconian! We are looking for everyone to join us in VALIDATION SPECIALIST position.

  • Degree in Pharmaceutical, Biomedical Engineering, Industrial Pharmacy, or related life sciences.
  • 1+ year of experience; fresh graduates welcome.
  • Knowledge in pharmaceutical/equipment validation, quality systems, and regulations.
  • CSV and GMP experience is a plus.
  • Strong technical writing, computer literacy, and English proficiency.
  • Analytical, focused, and able to work under pressure.
  • Willingness to work in a diverse environment and travel for site testing.
  • Verify design documents against specifications (URS/AOS).
  • Provide end-user insights to engineers for design alignment.
  • Attend DQ meetings and coordinate client specifications.
  • Create and update Validation Traceability Matrix (VTM).
  • Author and coordinate FAT and IQ/OQ protocols and schedules.
  • Liaise with suppliers for documentation; monitor validation progress.
  • Perform validation activities and draft necessary documents.
  • Conduct risk management and gap analysis for process deviations.

Join us and grow your career with Esco.

Esco BISA!

Only shortlisted candidates will be contacted.
Indonesia
20 September 2024
0
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