jobs in PM ASIA PROJECT SERVICES PTE. LTD.

全职 Commissioning and Qualification Engineer 工作, 薪水 up to SGD 6,000, PM ASIA PROJECT SERVICES PTE. LTD. Islandwide (Singapore) 公司招聘中 - Ricebowl

Commissioning and Qualification Engineer

PM ASIA PROJECT SERVICES PTE. LTD.

SGD6,000 - SGD6,000 每月

Islandwide (Singapore)

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工作地点

  • Islandwide (Singapore) Singapore

职位描述

岗位职责

Due to current demand, PM Group is currently looking to expand the CQV team.

Your day to day role would involve the following activities:

  • Planning, Performance, and Coordination of Computer System Validation, Equipment Qualification, Temperature Controlled Objects (Freezers, Incubator etc), Clean Utilities Validation and cleaning validation in accordance with internal procedures and industry standards.
  • The qualification includes, FAT, SAT, IQ, OQ, PQ of any additional / modifications of existing manufacturing process equipment, package units (e.g. Ultrafiltration Unit, Chromatography Columns, autoclave, FIT testers), commercial off the shelves (COTS) analytical instruments, freezers,
  • Experience to creates, reviews and approve equipment qualification and analytical instruments lifecycle documentations, e.g. FAT, SAT, IQ, OQ, PQ protocols and reports, risk assessments, technical specifications.
  • Can lead investigation revolving around discrepancies identified during qualification activities.

We would like to hear from candidates who have:

  • Experience in coordinating the commissioning and qualification activities (including the creation, pre-execution approval, execution, post-execution review, and post-execution approval of all validation lifecycle documents)
  • Experience in leading daily validation meetings with cross functional in resolving validation issues.
  • Experience in equipment qualification including analytical instrumentation and manufacturing equipment.
  • Experience in ASTM2500 of process equipment commissioning and qualification (Ultrafiltration units and chromatography column is preferred)
  • Relevant work experience in Pharmaceutical and/or Biopharmaceutical industries
  • Hands on validation execution experience
  • Review validation documents
  • Write validation protocols and reports
  • Able to execute activities in cGMP environment, including cleanrooms or technical areas.
  • Attention to detail



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