Job Summary

• This high-impact role is responsible for the development, validation, and technology transfer of manufacturing and cleaning processes, serving as the principal point of contact for all aspects of product and process knowledge.
• Key responsibilities include coordinating and executing process development and validation, authoring necessary documentation, analyzing stability data, and managing de-risking and business continuity projects.
• The role involves collaboration with various site functions for technical aspects of change controls, deviations, investigations, and supporting commercial production technology issues.

Matching Summary

Skills & Requirements

Key Requirements

• BS degree in Chemistry, Pharmaceutical Chemistry, or related area
• 1-5 years experience in a GxP pharmaceutical regulated environment
• Experience with process validation of pharmaceutical and dietary supplement products
• Strong relationship management skills
• Good knowledge of written and spoken English

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