Production Coordinator


Singapore, Southeast, Singapore - 00000

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate10 Oct, 2022Not Specified12 Jul, 20223 year(s) or aboveGood communication skillsNoNo
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Entrusted by Pfizer Singapore, Cielo Talent supports Pfizer to recruit permanent employees for the expansion of Pfizer Tuas manufacturing site in Singapore.


Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
To learn more, visit .
For additional information on our guidelines, please visit


How You Will Achieve It

  • Support the Process Engineers in the preparation of documentation required to launch a product campaign .
  • Monitor and maintain the plant documentation on a proactive basis, whilst continually reviewing the systems and procedures to identify areas for improvement. These documents include, but not limited to Recipe Change controls, Manufacturing Instructions, Record of Manual Operations, Documents related to cleaning, Change controls.
  • Co-ordinate the overall administration of the plant documentation in close liaison with the Operations Supervisor, Process and Operations Manager and the shift teams.
  • Batch record review for compliance to Good Documentation Practices.
  • Responsible as department document co-ordinator to issue and reconciled controlled copies of the operating and cleaning instructions, log books and any other documents to operations team.
  • Conduct day to day review of forms and documents to ensure Good Documentation Practice. Perform reconciliation on the forms and documents upon completion.
  • Ensure all documents are in completion and perform archival as necessary.
  • Coordinate with EHS and Warehouse team on waste disposal information pertaining to waste generated during operation.
  • Follow up CAPA actions when necessary.
  • Report all actual, near misses and potential accidents for further investigation when needed.
  • Raise purchase requisition for plant use and equipment relevant items when necessary.
  • Review and revise relevant Standard Operating Procedure when necessary.
  • Assist Day Lead Technician in terms of documentation related tasks when necessary.
  • Assist Day Supervisor in any documentation tasks when necessary.
  • Develop courses of action and drive implementation of solutions.
  • Uphold Pfizer’s code of conduct and values.
  • Accountable for:
  • Monitoring & Completion of Plant Documentation
  • Plant Documentation Preparation
  • Plant Administration
  • Trend Reporting & Analysis
  • Documentation preparedness
  • Plant reports on schedule
  • Metric measurement reports



  • Nitec or Diploma in a technical discipline
  • 3 years experience in a cGMP manufacturing environment
  • Fresh graduates are welcomed to apply.


  • Process & Plant Knowledge
  • Strong IT and reporting skills
  • cGMP and GDP Knowledge
  • Personal & Organization Skills

How To Apply:

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Please refer the Job description for details


Min:3.0Max:8.0 year(s)

Information Technology/IT

Production / Maintenance / Quality

Information Technology




Singapore, Singapore