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Zuellig Pharma is a leading healthcare solutions company in Asia, helping make healthcare more accessible through distribution, digital, and commercial services. This role focuses on reviewing, validating, and identifying accurate technical specifications for government bids to ensure regulatory compliance and proper classification of medicines.
You will analyze procurement requirements, verify dosage forms, packaging, and storage needs, and ensure bid submissions meet project specifications.
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.
Responsible for reviewing, validating and identifying accurate technical specifications of pharmaceutical products required for government bids. To ensure that all medicine specifications, regulatory requirements, and product to offer will comply with bidding criteria applicable to pharmaceutical regulations. Achievement of Bid qualification to contribute sales target attainment of government channel.
Qualification and Education Requirements:
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.