Hiring: Pharma Manufacturing QA Site Supervisor

Pharma Manufacturing QA Site Supervisor (Must have API Pharma Exp/ Strong in QA Site Work) Up 12K #HJC

Singapore | Posted: Sep 24, 2026

Site Quality Management

• Lead and manage on-site quality assurance activities in manufacturing, packaging, warehouse and supporting areas to ensure compliance with GMP, the Quality Management System (QMS), and applicable regulatory requirements.
• Develop Site QA work plans and allocate resources for routine shop-floor monitoring, GMP walkthroughs, documentation review and material release activities.
• Supervise, coach and develop Site QA personnel to ensure consistent and effective execution of assigned quality oversight activities.
• Conduct routine GMP inspections, focused audits, internal self-inspections and quality risk assessments; identify, escalation and drive timely resolution of quality and compliance issues.
• Provide real-time QA oversight of critical manufacturing activities, process controls, line clearance, material status labeling, personnel practices, housekeeping, documentation practices and data integrity.
• Work closely with Manufacturing, Warehouse, QC, Engineering and Validation functions to resolve site quality issues and drive continuous improvement.

Material Release

• Review and approve documentation supporting the release of raw materials and packaging materials for use, ensuring compliance with approved supplier status, testing status, storage requirements, labeling and applicable specifications.
• Oversee Site QA activities related to material release, material status control and disposition of non-conforming or abnormal materials.
• Review master cleaning records, line clearance records, SOPs and related controlled documents to ensure GMP compliance and alignment with actual site practices.

Cleaning Validation System

• Establish, maintain and continuously improve the site cleaning validation program and associated quality system.
• Develop, review and approve cleaning validation policies, SOPs, validation plans, protocols, reports and related technical documentation.
• Lead or coordinate cleaning validation risk assessments, including equipment and product grouping, worst-case product selection, residue limit establishment, sampling strategies, analytical methods, acceptance criteria and revalidation requirements.
• Review and approve cleaning validation protocols, cleaning validation reports, cleaning verification reports and periodic review reports.
• Provide QA oversight during cleaning validation execution
• Review cleaning-related deviations, changes, CAPAs and impact assessments, and assess potential impact on product quality, cross-contamination control and validation status.
• Conduct periodic review of cleaning procedures and validation status, identify revalidation needs, and implement continuous improvements to cleaning processes and cross-contamination control measures.

Deviation, Change Control and CAPA Management

• Lead or participate in investigations, assessment, review and follow-up of deviations, incidents, change controls, quality risk assessments and CAPAs related to site operations.
• Lead cross-functional investigations for critical, recurring or systemic quality issues and ensure robust root cause analysis is performed.
• Ensure corrective and preventive actions are implemented within agreed timelines and verify their effectiveness.
• Perform periodic trend analysis of deviations, audit findings, cleaning-related issues and other site quality metrics to identify improvement opportunities.

Customer Audit and Regulatory Inspection Management

• Lead Site QA preparation, coordination and support for customer audits, regulatory inspections, third-party audits and internal audits.
• Act as the primary Site QA contact for matters related to shop-floor quality management, material release, cleaning management and cleaning validation during audits and inspections.
• Coordinate the preparation and review of audit documentation, including material release records, cleaning and line clearance documentation, cleaning validation documents, deviations, change controls and CAPA evidence.
• Support audit hosting, coordinate responses to audit observations, and ensure responses are accurate, timely and scientifically justified.
• Develop and review audit remediation plans, assign responsible owners and due dates, and track CAPA completion and effectiveness.
• Maintain awareness of Singapore Health Sciences Authority (HSA) GMP requirements and relevant regulatory expectations in target markets.

Team Leadership and Quality System Improvement

• Manage Site QA team performance, including recruitment support,