QC Digital Systems Lead — LabWare LIMS & Compliance

P-CON MANAGEMENT PTE. LTD.; Singapore; On-site; SGD 90,000 - 120,000; Full time

Job summary

P-Con Management is seeking a QC digital systems specialist to bridge quality control operations with digital transformation. You will deploy and maintain LabWare LIMS and other GxP laboratory systems, ensuring data integrity and regulatory compliance within a regulated lab.

Responsibilities include method validation, equipment qualification, investigations of quality events, and end-user training, while upholding cGMP, Data Integrity and HSE standards and supporting audits.

Qualifications

• Experience with analytical method validation and equipment qualification.
• Knowledge of cGMP, data integrity, and HSE requirements.
• Experience with QC digital systems and LabWare LIMS deployment/maintenance.

Responsibilities

• Maintain, and administer QC digital systems (including LabWare LIMS), managing master data, user access, and related documentation.
• Plan and execute preventive maintenance, calibration, and qualification of QC lab equipment, ensuring GxP compliance and audit readiness.
• Investigate and resolve QC events and deviations, and drive CAPAs and continuous improvement initiatives.
• Prepare and review qualification/validation documentation (protocols, risk assessments, reports) and support change control for QC test methods.
• Train and support end-users on QC digital tools, and support regulatory inspections and audits.
• Ensure all work complies with cGMP, Data Integrity, and HSE requirements.

Skills

GxP compliance

Data integrity

Regulatory audits

Quality systems

Tools

LabWare LIMS

Job description

P-Con Management is seeking a QC digital systems specialist to bridge quality control operations with digital transformation. You will deploy and maintain LabWare LIMS and other GxP laboratory systems, ensuring data integrity and regulatory compliance within a regulated lab.

Responsibilities include method validation, equipment qualification, investigations of quality events, and end-user training, while upholding cGMP, Data Integrity and HSE standards and supporting audits.