Job Description

• 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 are collected, reviewed & monitored.

• Conduct GMP Training in the factory & ongoing training for QC team.

• Conduct investigation in a customer complaint, return & counterfeit product.

• Ensure environmental monitoring is conducted.

• Ensure rejection & disposal of materials are done properly.

• Ensure Good Documentation Practices & traceability in place.

Job Requirement

• Minimum bachelor\xe2\x80\x99s degree in Pharmaceutical, Bioscience, Chemical or related courses.
• Minimum 5 years of working experience in GMP environment.
• Working knowledge of GMP & ISO.
• Hands-on experience in equipment qualification & validation will be an advantage.
• Positive working attitude.
  

Janet Lim Chia Ee EA License: 11C2878 EA Registration No: R1981865