QC Associate - Equipment Qualification & Validation (Pharma)

Manpower Singapore; Singapore; On-site; SGD 47,000 - 78,000; Full time

Benefits offered by this job

Completion bonus

Job summary

Manpower Singapore is recruiting on behalf of our client for a QC Associate - System Support (Equipment Qualification/ Validation) in Singapore. The role focuses on updating validation master plans, supporting method control and data evaluation, and managing QC lab equipment lifecycle in a GMP environment.

You will ensure proper documentation, support investigations, and participate in regulatory inspections, with emphasis on data integrity and cGMP compliance.

Qualifications

• Minimum 5 years of QC experience in pharma with GMP knowledge.
• Bachelor's degree in Pharmacy or related life sciences.
• Detail-oriented with testing accuracy and regulatory compliance.
• Solid understanding of laboratory practices and data integrity.
• Experience with analytical method monitoring and CAPA processes.

Responsibilities

• Update validation master plans and procedures for GXP lab equipment.
• Support method control trend reviews and data evaluation.
• Manage lifecycle of QC lab equipment qualification and review.
• Document qualification and maintenance deliverables with risk assessments.
• Assist in regulatory inspections and audits.
• Prepare metrics for qualification and validation activities.
• Contribute to continuous improvement of QC equipment management.

Skills

GMP knowledge

Lab instrumentation

Data integrity

Documentation practice

Education

Bachelor's degree in Pharmacy / Pharmaceutical Sciences / Chemistry / Biology or related 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.