Responsibilities

• • Lead & support QC team for daily QC activities for incoming materials checks & production online checks.
  • Ensure GMP compliance in production & manufacturing facilities.
  • Approve for release or reject incoming materials, bulk oil & finished products.
  • Data & trend analysis on all QC checks for Product Quality Review.
  • Review & approve Batch Process Records.
  • Handling quality issues & manufacturing deviations for incoming materials & production operations.
  • Follow up CAPA & ensure the implementation in place.
  • Establish, review & update SOP, Work Instructions, charts & other documents in QC department.
  • Ensure all measuring devices are verified & calibrated.
  • Support production equipment qualification, validation, machine test & trial run.
  • Ensure all QC labels are controlled & pasted accordingly.
  • Ensure retention samples collected, reviewed & monitored.
  • Conduct GMP Training in factory & ongoing training for QC team.
  • Conduct investigation in customer complaint, return & counterfeit product.
  • Ensure environmental monitoring is conducted.
  • Monitor accelerated & real time stability studies.
  • Ensure rejection & disposal of materials are done properly.
  • Ensure Good Documentation Practices & traceability in place.

Requirements

• • Minimum Bachelor’s Degree in Pharmaceutical, Chemistry & other relevant courses.
  • Minimum 5 years of working experience in GMP/Pharma Company
  • Working knowledge of GMP & ISO.

To find out more about this opportunity, please contact Lionel Liew at lionel.liew@gmprecruit.com.

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793 |   EA Personnel: Lionel Liew   |   Registration No: R1330693