Job Description

A leading consulting firm is looking for a GMP Pharmaceutical Technical Writer to produce and maintain essential documentation in the pharmaceutical industry. Responsibilities include authoring Standard Operating Procedures, ensuring compliance with GMP regulations, and collaborating with cross-functional teams. The ideal candidate holds a Bachelor’s degree in Life Sciences with at least 2 years experience in a GMP-regulated environment. Strong communication skills and proficiency in document management systems are essential, along with the ability to work independently on multiple projects.
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