Join our dynamic team where innovation and care converge in a culture that values continuous learning, diversity and transformative career development. Underpinned by THRIVE with Zuellig Pharma, our commitment to transforming the way we grow, care and succeed together as one organization, we are dedicated to helping our people make a meaningful impact in healthcare.
Quality Control Specialist
Singapore
Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world-class distribution, digital, and commercial services to support the growing healthcare needs in this region.
The company was started a hundred years ago and has grown to become a multibillion-dollar business covering 17 markets with over 12,000 employees. Our people serve more than 200,000 medical facilities and work with over 450 clients, including the top 20 pharmaceutical companies in the world.
Purpose of The Role:
To support Quality Control (QC) operations by ensuring all packaging material activities and QC releases are performed in compliance and GxP standards, client requirements, and regulatory guidelines.
What You’ll Do:
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Perform sampling, inspection, and release of incoming packaging materials.
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Maintain and manage packaging material specifications and related documents.
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Update QC logs, records, and trackers accurately and in a timely manner.
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Conduct other QC inspections and releases as required (e.g. inbound QC release, cold chain temperature release, outbound release).
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Independently communicate and collaborate with internal terms, external parties, and regulatory stakeholders on QC matters.
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Ensure full compliance with ISO procedures, GxP standards, and regulatory requirements.
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Maintain general cleanliness and hygienic conditions of workstations.
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Support calibration and maintenance of QC-related equipment and measuring instruments.
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Assist in internal end external audits related QC activities
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Support deviation management, and Corrective and Preventive Actions (CAPA) related to QC functions.
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Perform backup duties and any other tasks as assigned.
Must-Have:
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Diploma in a relevant discipline, or strong knowledge in Quality / Compliance within a manufacturing environment.
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Proven experience in Quality Control, or Quality Assurance in manufacturing, production, assembly, or operations settings.
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Willingness to work flexible hours, including shifts, extended hours, weekends, and public holidays, based an operational needs.
Advantage to Have:
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Knowledge of ISO, GMP, and GSDP standards.
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Working knowledge of SAP systems.
What We Offer:
• We are committed to fostering an inclusive environment where our employees can learn, grow, and achieve shared success.
• We champion diversity, equity, and inclusion, ensuring every individual feels valued, respected, and treated fairly.
• As a leading multi-market healthcare solutions provider, we empower our employees to gain comprehensive knowledge and expertise in the dynamic healthcare industry across the region.
• Enjoy the flexibility to effectively balance your work and personal life while taking charge of your career journey through our empowering growth opportunities.
• Our Total Rewards program is designed to support your overall well-being in every aspect.
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