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

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD; Singapore; On-site; SGD 69,000 - 83,000; Part time

Benefits offered by this job

Completion bonus 1 month

Job summary

MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD seeks a QC Associate - System Support to assist equipment qualification and validation in a GMP pharma setting. The role emphasizes cGMP compliance, data accuracy, and timely documentation.

Ideal candidates hold a Bachelor’s degree in pharmacy or related life sciences, with at least 2 years in QC; responsibilities include master plans, method monitoring, equipment lifecycle, investigations, and audits.

Qualifications

• Minimum of two (2) years of experience in quality control within the pharmaceutical industry, including good knowledge of GMP and regulatory requirements.
• Hands-on exposure and theoretical requirement of QC laboratory instruments and ALCM management.
• Bachelor's Degree in Pharmacy or related life sciences/technology.

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 for their intended use.
• Decommissioning of QC equipment and maintaining up to date the lab equipment inventory.
• Participate in documentation issuance and review of qualification and maintenance deliverables such as risk assessments, traceability matrices, protocols, reports, deviations, and summary reports.
• Support laboratory qualification investigations and resolving quality control events, issues or discrepancies from his/her perimeter; implement remediation actions from findings and CAPAs.
• Provide support during regulatory inspections and audits.
• Prepare metrics and monitoring data for 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 with QC excellence team.
• Record all expected raw data, calculations, information related to tasks to comply with cGMP and data integrity.

Skills

GMP knowledge

cGMP

Data integrity

Documentation practice

Analytical method monitoring

Lab equipment qualification

Education

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

Job description

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

6 Months Contract

Location : Gul Circle

Salary Up to $6,800 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 two (2) 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.
• Strong interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.