QC Associate - Equipment Qualification & System Support

Manpower Staffing Services; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A global healthcare company in Singapore is seeking a QC Associate for Equipment Qualification & System Support. The role requires a Bachelor's Degree and a minimum of two years' experience in pharmaceutical quality control. Responsibilities include managing validation plans, supporting lab equipment qualification, and ensuring compliance with GMP and regulatory requirements. This position offers a competitive salary and completion bonus.

Benefits

Completion Bonus

Competitive salary

Qualifications

• Minimum of two years of experience in quality control within the pharmaceutical industry.
• Hands-on exposure to QC laboratory instruments and ALCM management.
• Good understanding of good laboratory practices and data integrity requirements.

Responsibilities

• Updating the site validation master plan and procedures for GXP lab equipment.
• Support periodic analytical method control trend review and data evaluation.
• Documenting qualification and maintenance deliverables, such as protocols and reports.

Skills

Good knowledge of Good Manufacturing Practices (GMP)

Proficiency in identifying issues and implementing solutions

Keen attention to detail

Education

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

Tools

QC laboratory instruments

Job description

QC Associate - Equipment Qualification & System Support

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

Location: Gul Circle
Salary: Up to $5,000 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 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.
• Excellent interpersonal relationships to establish the partnerships necessary for the development of the Quality culture.