Responsibilities

• Conduct sampling & QC checks for incoming materials, bulk oil & finished products.
• Make sure the starting materials, intermediate & finished product meet specifications.
• Record & review Batch Process Records.
• Follow up approval for release or reject incoming materials, bulk oil & finished products.
• Print & control all QC labels to ensure labels are pasted accordingly.
• Maintain 5S, control & limit the access in in QC areas.
• Conduct internal verification of measuring equipment & send out for external calibration.
• Support production equipment qualification, validation, machine test & trial run.
• Follow up quality issue, deviation, investigation & CAPA for all QC operations.
• Conduct air sampling for environmental monitoring.
• Ensure retention samples collected, reviewed & monitored.
• Assist in product complaints, recall, return, reject & disposal.
• Conduct GMP Training in factory & ongoing training for QC team.
• Conduct investigation in customer complaint, return, reject & counterfeit product.
• Maintain data, records & documents for traceability & audits.

Requirements

• Minimum diploma in Pharmaceutical, Bioscience, Chemical or related courses.
• Minimum 2 years of working experience in Pharmaceutical & GMP company.
• Working knowledge of GMP & ISO.
• Hands-on experience in equipment qualification & validation will be an advantage.

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