PR/160260 | QA / QM Associate

Company and Job Overview
Our client specializes in manufacturing and selling medicinal and pharmaceutical products. As part of their expansion, they are now seeking a QA/QM Associate to manage QA/QM activities for Malaysia and Singapore.

Job Responsibilities

• Oversees quality documentation, including drafting/revising SOPs and maintaining compliant quality records and document control systems
• Administers training programs, manages the e‑learning system, and delivers GDP onboarding and refresher sessions
• Manages quality systems, including change control, deviations, complaints, returned goods, CAPA tracking, PQR coordination, and annual quality reviews
• Ensures regulatory and GDP compliance, supporting inspections, managing product release/redressing compliance, and conducting mock recalls
• Oversees vendor quality, including qualification, performance tracking, issue resolution, and support for vendor audits
• Collaborates cross‑functionally and supports regional/global quality initiatives to ensure compliant operations across the business

Job Requirements

• Bachelor’s degree in Pharmacy, Life Sciences, or related discipline
• Possesses 1–3 years of experience in pharmaceutical QA
• Has a solid grasp of GDP, GMP, PIC/S, ICH standards, as well as local NPRA regulations
• Able to interpret global SOPs and tailor them to meet local regulatory requirements
• Shows strong analytical and problem‑solving capabilities, particularly in understanding complex regulatory frameworks
• Exhibits excellent organizational skills and effective process management
• Adaptable and able to perform well in a fast‑changing regulatory environment
• Displays a strong sense of ownership and works independently with minimal supervision

• Brings strong teamwork and stakeholder management skills, collaborating effectively with regulatory, supply chain, commercial, and regional/global QA teams

   

Interested applicants, feel free to click APPLY NOW.

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