A leading services supplier in Puerto Rico is seeking a talented TOP Documentation Specialist. This role involves managing the collection, review, and delivery of key documentation for packaging line equipment in a GMP-regulated environment. Ideal candidates will have at least 3 years of experience in document control within a pharmaceutical or biotech setting and possess strong organizational skills and attention to detail. Proficiency in document control software such as Veeva or MasterControl is essential. Competitive benefits and a commitment to ethical standards are offered.
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