Editorial summary

The company is seeking a QA Site Head for its pharmaceutical manufacturing plant to oversee site quality management, ensure product quality, and meet client expectations. The role involves establishing, optimizing, and maintaining the quality system, ensuring regulatory compliance, and reviewing quality procedures and manuals. Candidates should have experience in quality system management, deviation investigation, and continuous improvement processes. The position offers a salary of 25,000.

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Job description

[This job id 28263 first appeared in Job-Q.com on 28 Aug 2026]

• Be responsible for site quality matters, ensure the product quality and meet client’s quality expectations.
• Responsible for establishing, optimization and maintenance of the quality system, ensure that the site quality activities comply with quality management requirements
• Review and approve quality procedures, quality manuals, annual/month quality review.
• Establish, optimize and maintain the company quality system, ensure the regulator’s compliance and operability
• Define effective CAPAs, ensure the continuous improvement of the quality system by deviation investigation, quality incident handling, quality review, self-inspections and external inspections.
• Follow client quality agreement, meet client’s quality expectations.
• Host client auditing, respond to the audit report and follow up the actions.
• Review and approve VMP and validation documents.
• Organize quality training, promote employee quality awareness and company quality culture.
• Notify top management and responsible management team in a timely manner regarding quality issues, quality trending etc.
• Comply with national and local EHS laws and regulations, and strictly implement all EHS policies, SOPs and rules of the Company.
• Participates in EHS working conference, EHS training, fire drill and other activities, continually learning EHS knowledge and improving skills, enhancing safety awareness, and actively participating in the establishment of EHS culture.
• Pharmacy or chemistry related major, university degree or above.
• Understand pharmaceutical production, testing and quality management, be familiar with GMP related regulations.
• Quality management related experience in pharmaceutical factory.
• Good leadership skills, guide and supervise subordinates; responsible for work assignment, assessment and motivation of subordinate staff

VeronicaNeo Shen Hwa  -

Personnel Reg No: R1110855

Manpower Staffing Services (S) Pte Ltd

EA Licence No: 02C3423

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