• Leading Homegrown Medical Brand  
• Working Location: Central East

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.
• At least 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.
• Positive working attitude.

To apply, please visit to www.gmprecruit.com and search for Job Reference: 19359

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