• Leading Homegrown Medical Brand  
• Working Location: Central East

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.
• At least 5 years of working experience in GMP/Pharma Company
• Working knowledge of GMP & ISO.
• Hands-on experience in equipment qualification & validation will be an advantage.
• Positive working attitude.

To apply, please visit to www.gmprecruit.com and search for Job Reference: 19358

To find out more about this opportunity, please contact Alexandra at: alexandra@gmprecruit.com

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Alexandra Calingo | Registration No: R1101491