Job Purpose
Responsible for the execution of all aspects of solid-dosage manufacturing which includes but is not limited to packout of finished goods bottles. In addition, responsible for all cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation.
Essential Duties and Responsibilities include the following. Other duties may be assigned:
To perform this job successfully, an individual should have:
Education and/or Experience:
Education: High School Diploma or GED Equivalent, bachelor’s degree in physical sciences or pharmaceutical life science related field of study.
Years of related experience and/or training
3-10 years related experience in cGMP production/packing operation activities.
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