QC Associate

QC Associate - Equipment Qualification & System Support

This range is provided by Manpower Singapore. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Overview

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.

Base pay range

Location: Gul Circle
Salary Up to $5,000 depending on experience
Completion Bonus 1 Month

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, and recommend method improvements where appropriate.
• Support the life cycle management of the QC lab equipment, i.e., qualification of QC equipment and periodic review 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 investigations and resolving any quality control events, issues or discrepancies within their 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 in coordination with the QC excellence team.
• Support the invalid assay trending program in the QC laboratory.
• Record all expected raw data, calculations, and information related to tasks to comply with cGMP and data integrity requirements.
• Perform tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, and records.

Requirements

• Minimum of two (2) years of experience in quality control within the pharmaceutical industry, including good knowledge of GMP and regulatory requirements, with hands-on exposure and theoretical understanding 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 regulatory compliance.
• Proficiency in identifying issues and implementing effective solutions to resolve quality control problems.
• Good understanding of GxP, good laboratory practices, good documentation practice and data integrity requirements.
• Experienced in analytical method continuous monitoring requirements.
• Excellent interpersonal relationships to establish partnerships needed for developing a quality culture.

Lim Pey Chyi -
Recruitment Consultant (R )
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423

Desired Skills and Experience

Minimum of two (2) years of experience in quality control within the pharmaceutical industry, including GMP knowledge and regulatory requirements, with hands-on exposure and theoretical requirement of QC laboratory instruments and ALCM management. A Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biology or related life sciences or Technology is preferred. Strong attention to detail and problem-solving abilities, plus good laboratory practices and data integrity understanding.

Apple, Pey Chyi Lim EA License No.: 02C3423 Personnel Registration No.: R

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Seniority level : Associate

Employment type : Contract

Job function : Quality Assurance and Science

Industries : Pharmaceutical Manufacturing

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