4 months QC Specialist (Equipment Qualification, Protocol Writing, Pharmaceutical MNC) #HCG

Responsibilities

• Perform equipment qualification activities, including preparation and execution of qualification protocols and reports.
• Develop, review, and maintain equipment qualification documents in compliance with cGMP and applicable quality standards.
• Support QC release activities, including sampling, testing, and disposition of raw materials and finished products or packaging components.
• Perform routine laboratory equipment maintenance, calibration, and preventive maintenance in accordance with established procedures.
• Support the investigation and management of rejected, quality-hold, and non-conforming materials.
• Ensure compliance with cGMP requirements, SOPs, and laboratory safety procedures.
• Maintain timely completion of mandatory training and qualification documentation.
• Participate in continuous improvement initiatives to enhance QC processes and quality systems.

Requirements

• Degree in Science or equivalent, with at least 2 years of relevant experience in the pharmaceutical or chemical manufacturing industry; or
• Diploma in Chemistry, Life Sciences, Pharmaceutical Science, or a related discipline, with at least 5 years of relevant experience.
• Experience in equipment qualification and protocol writing is preferred.
• Hands-on experience operating laboratory equipment such as FTIR, Cytation microplate reader, Sysmec, HPLC.
• Good understanding of cGMP requirements, documentation practices, and quality systems.

All qualified applicants, please send in your resume to:

[email protected]

Tricia Celestine Goh (R1981653)

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