Editorial summary

The Senior QC Chemist (Pharma MNC) is responsible for providing comprehensive testing and analytical services to the plant to ensure products meet specifications, quality, and safety goals, on schedule. The role involves performing biochemistry, analytical, and raw material/in-process/finished product testing for lot release in compliance with GMP, and maintaining appropriate records, including method transfer testing. The company is a pharmaceutical multinational corporation, and the position requires careful adherence to quality standards and timely reporting. The offered compensation is 6,000 per month.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/senior-qc-chemist-pharma-mnc-4k-to-6k-hkh-37474 first appeared in Job-Q.com on 12 Oct 2026]

Primary Goals/Objectives:

To provide an effective testing and analytical service to the plant ensuring that products manufactured are tested to specification on time and plant quality and safety goals are met.

Ensure that all raw material, in-process and finished product testing and method transfer testing is carried out per schedule and per GMP. Ensure that records are maintained to appropriate requirements.

Major Responsibilities:

• Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures.
• Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath and etc.
• Support laboratory operations including but not limited to method transfer, equipment qualification, calibration, cleaning and maintenance, purchase and receipt of reagents and consumables, waste management, reagent and media preparation, critical reagent management and document management.
• Review lot release data, identify testing discrepancies and participate in laboratory investigations.
• Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
• To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
• To carry out completion and review of GMP Documentation of data sheets or LIMS software.
• To carry out QC sample receipt, assay and release procedures.
• Support Audit preparation and any audit related activity
• Reading and understanding the test procedure and the requirements per USP, JP and EP.

Requirements:

• min. Bachelor Degree in Biochemistry and above
• Min 2 to 3 years of HPLC / GC experience in pharma industry
• Able to do 12 hour rotating day and night shift OR Office Hours

Interested applicants, please forward your resume to

Consultant: Huang Jingsheng Kevyn (R1333338)
Recruit Express Pte Ltd (99C4599)

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