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Open nowPosted 9 days ago

Project Coordinator [Documentation | Pharma MNC | Joo Koon] RRKC

MyCareersFuture94,028 open roles

Pay
SGD 4,500 – SGD 5,500 a month
Where
Singapore
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Your applicationOpen nowProject Coordinator [Documentation | Pharma MNC | Joo Koon] RRKCMyCareersFuture · Singapore

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  2. 3.3%3 days
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  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 9 days ago

The posting

Job Summary

  • Pharmaceutical US MNC @ Joo Koon
  • 12 Months Renewable Contract
  • Up to $5,500/month + 1-month bonus
  • Monday - Friday, 8AM - 515Pm

Key Responsibilities

  • Prepare, issue and review batch manufacturing records.
  • Review completed batch records for accuracy, completeness, data integrity and cGMP compliance.
  • Support batch release and disposition activities.
  • Maintain manufacturing and quality documentation according to approved procedures.
  • Support updates to SOPs, Work Instructions, forms and controlled documents.
  • Maintain manufacturing compliance and training records.
  • Identify opportunities to improve documentation quality and manufacturing processes.

Technology Transfer & Project Support

  • Support technology transfer projects from initial planning through manufacturing readiness and handover.
  • Coordinate project timelines, milestones, resources, risks and key activities.
  • Work with cross-functional teams including Manufacturing, Quality, Validation, Engineering, Regulatory and Supply Chain.
  • Track transfer documentation, validation activities, analytical method transfers and GMP requirements.
  • Identify project risks and coordinate solutions with relevant teams.
  • Provide regular project updates on progress, timelines, risks and key decisions.
  • Support multiple projects and ensure activities are completed on schedule.

Role Requirements

  • Diploma or Degree in Engineering, Life Sciences, Pharmaceutical Science, Manufacturing or a related discipline.
  • Experience in pharmaceutical / biotech manufacturing, GMP documentation or technology transfer is preferred.
  • Experience with batch records, SOPs and controlled documentation is an advantage.
  • Good understanding of cGMP and data integrity requirements.
  • Strong project coordination and organisational skills.
  • Good communication and stakeholder management skills.
  • Able to work independently and collaborate effectively with cross-functional teams.
  • Good attention to detail and ability to manage multiple projects and deadlines.

If you are keen to explore this career opportunity, kindly send a copy of your resume to [email protected] or simply click the button to APPLYNOW! We regret that only shortlisted applicants will be notified.

Chan Ku Ci - R22111446 EA License No: 16C8261

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