QC Associate - System Support (Equipment Qualification&Validation)

Manpower Staffing Services (Singapore) Pte Ltd; Singapore; On-site; SGD 47,000 - 78,000; Full time

Job summary

ManpowerGroup is seeking a QC Associate - System Support (Equipment Qualification/Validation/Pharma) for a role based at Gul Circle, Singapore. The candidate will join a critical QA function supporting equipment qualification, validation and lifecycle management of QC lab instruments.

Requires at least 5 years in pharmaceutical QC with GMP knowledge, and a degree in Pharmacy or Life Sciences. A completion bonus of 1 month is offered and salary is up to SGD 7,000 depending on experience.

Qualifications

• Minimum of 5 years of experience in quality control within the pharmaceutical industry.
• Hands-on exposure to QC laboratory instruments and ALCM management.
• Knowledge of GMP and regulatory requirements; data integrity aware.

Responsibilities

• Update validation master plans and procedures for GXP lab equipment and ALCM.
• Support method control trend reviews, data evaluation and improvements.
• Oversee QC lab equipment qualification and periodic review for intended use.
• Decommission equipment and maintain accurate lab inventory.
• Prepare documentation such as risk assessments, protocols and deviation reports.
• Assist investigations and CAPA remediation for QC events.
• Support regulatory inspections and audits.
• Generate metrics for qualification/validation activities and identify trends.
• Drive continuous improvement in QC equipment management with the QC excellence team.
• Record all raw data and calculations to ensure cGMP and data integrity compliance.
• Perform tasks in line with cGMP and HSE requirements.

Skills

GMP knowledge

Data integrity

QC instruments

Attention to detail

Education

Bachelor's degree in Pharmacy or Life Sciences

Job description

QC Associate - System Support (Equipment Qualification/ Validation/ Pharma)

Location : Gul Circle

Salary Up to $7,000 depending on experience

Completion Bonus 1 Month

Our client delivers vital healthcare solutions worldwide, powered by the precision and dedication of its Manufacturing & Supply teams. With your talent, they can expand their impact-protecting more people and offering hope to patients and their families.

Responsibilities

• Updating the site validation master plan and procedures related to ALCM and CPV of GXP lab equipment.

• Support periodic analytical method control trend review/ investigation and data evaluation on method performance, recommend method improvements where appropriate.

• Support the life cycle management of the QC lab equipment i.e qualification of QC equipment and periodic review are maintained for their intended use.

• Decommissioning of QC equipment and maintaining up to date the lab equipment inventory.

• Participate in proper documentation issuance and review of qualification and maintenance deliverables, such as risk assessments, traceability matrices, protocols, reports, deviations, and summary reports.

• Support laboratory qualification Investigation and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs.

• Providing support during regulatory inspections and audits.

• Prepare metrics and monitoring data for the qualification and validation activities, to identify trends and issues, during life cycle management of QC laboratory equipment.

• Support initiatives for continuous improvement in QC support processes related to lab equipment management in coordination with QC excellence team.

• Support invalid assay trending program in the QC laboratory.

• Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements.

• Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks.

Requirements

• Minimum of 5 years of experience in quality control within the pharmaceutical industry, including good knowledge of Good Manufacturing Practices (GMP) and regulatory requirements, with hands‑on exposure and theoretical requirement of QC laboratory instruments and ALCM management.

• Bachelor's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life Sciences or Technology

• Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements.

• Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.

• Good understanding of good laboratory practices, good documentation practice and data integrity requirements.

• Experienced in analytical method continuous monitoring requirements.

• Excellent interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.

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