Job Description

A forward-thinking pharmaceutical consultancy in Singapore seeks a Quality Assurance Specialist to oversee GMP documentation and ensure compliance within a cGxP environment. The ideal candidate will manage documentation lifecycle activities, support training records, and uphold data integrity principles. This role requires a diploma or degree in a relevant field and strong interpersonal and analytical skills. The company offers a generous leave policy and professional development opportunities, fostering an inclusive culture where innovation thrives.
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