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Responsibilities:
. Revise and review Standard Operating Procedures (SOPs) to ensure compliance and quality standards.
. Review executed Manufacturing Batch Records (MBR) / Equipment Batch Records (EBR) for completeness and accuracy.
. Provide quality oversight and support to the manufacturing team, addressing any quality-related queries, concerns, or issues.
. Participate in GMP (Good Manufacturing Practices) and GEMBA walks to ensure adherence to quality standards on the shop floor.
. Provide quality support for Change Control processes, ensuring compliance with quality standards.
. Manage and review deviations, ensuring thorough investigations and timely closure.
Requirements:
. Minimum of 2 years of experience in the pharmaceutical or biopharma industry (preferred), including experience in batch record review, SOP revisions, or quality assurance oversight
. Experience in GMP and operational oversight activities (e.g., GEMBA, GMP walks) is advantageous.
. Experiene in Manufacturing Batch Records (MBR) / Equipment Batch Records (EBR)
If you are interested in the position, do kindly drop your most updated resume to [Confidential Information]
Kailey Lee Jia Yueh
EA Personnel No: R24126040
Recruit Express Pte Ltd (Healthcare & Lifesciences Division)
EA License: 99C4599
Date Posted: 09/09/2025
Job ID: 125801993