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

Roles & Responsibilities

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

Location : Gul Circle

Salary Up to $6,000 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

Lim Pey Chyi - Apple.lim@manpower.com.sg

Recruitment Consultant (R2090579)

Manpower Staffing Services (S) Pte Ltd

EA Licence : 02C3423

Tell employers what skills you have

Pharmaceutical Industry

Remediation

Quality Control

Trend

Staffing Services

Healthcare

Investigation

Traceability

Chemistry

Biology

Equipment Qualification

Audits

Regulatory Requirements

Life Sciences

Laboratory

Manufacturing