Contract QA Technician – Pharmaceutical Manufacturing #HHLT

Recruit Express Pte Ltd; Singapore; On-site; SGD 29,000 - 31,000; Full time

Job summary

Recruit Express Pte Ltd is seeking a quality-focused professional to support GxP manufacturing activities at our Tuas site. You will review manufacturing records, investigate deviations, and help prepare batch records in a fast-paced, regulated environment.

This 1-year contract involves rotating shifts, including public holidays, with a base salary of SGD 2,200–2,400 plus a 400 transport allowance. You will collaborate with cross-functional teams to ensure compliance with the Quality Management

Qualifications

• Min. NITEC qualification.
• Willing to rotate shifts including Public Holidays.
• Detail-oriented with quality documentation experience.
• Able to work in a regulated manufacturing/cleanroom environment.

Responsibilities

• Review GxP manufacturing records to ensure specifications and quality requirements are met.
• Review exceptions, deviations and critical alarms to support batch release activities.
• Perform quality walkdowns in manufacturing areas and cleanrooms.
• Manage GxP documents and samples, including distribution, review, approval, archival and disposal.
• Issue Manufacturing Batch Records (MBRs) and coordinate label printing.
• Support LIMS activities and ensure documentation accuracy.
• Support quality and process improvement initiatives.
• Conduct and support customer complaint investigations and trend complaint data.
• Work with cross-functional teams on investigations and CAPA implementation.
• Ensure compliance with Quality Management System and safety requirements.

Skills

Detail-oriented

Quality documentation

GxP knowledge

Education

NITEC

Tools

LIMS

Job description

Tuas
Mon–Fri, including Public Holidays
3 Rotating Shifts – 8 Hours Each
$2,200–$2,400 Basic + Shift allowance
$400 Transport Allowance
1-Year Contract

Responsibilities

• Review GxP manufacturing records to ensure specifications and quality requirements are met
• Review exceptions, deviations and critical alarms to support batch release activities
• Perform quality walkdowns in manufacturing areas and cleanrooms
• Manage GxP documents and samples, including distribution, review, approval, archival and disposal
• Issue Manufacturing Batch Records (MBRs) and coordinate label printing
• Support LIMS activities and ensure documentation accuracy
• Support quality and process improvement initiatives
• Conduct and support customer complaint investigations and trend complaint data
• Work with cross-functional teams on investigations and CAPA implementation
• Ensure compliance with Quality Management System and safety requirements

Requirements

• Min. NITEC
• Comfortable working rotating shifts, including Public Holidays
• Detail-oriented and comfortable working with quality documentation
• Able to work in a regulated manufacturing / cleanroom environment