Also referred to as: Analytical Development Supervisor, Biologics Process Development Supervisor
Requirements and Responsibilities

Biopharma Process Development Supervisor supervises a team of scientists who design and develop processes for the manufacturing of experimental and active drugs. Monitors the physical, chemical, and instrumental analysis of pharmaceutical ingredients to ensure efficiency and safety. Being a Biopharma Process Development Supervisor reviews, troubleshoots, and resolves issues to ensure adherence to formulary specifications. Analyzes and interprets results and makes recommendations for process improvement. Additionally, Biopharma Process Development Supervisor may lead more complex projects. Stays current on emerging technologies and trends within the biopharma industry. Requires a bachelor's degree in biology, chemistry, or a related field. Typically reports to a manager. The Biopharma Process Development Supervisor supervises a group of primarily para-professional level staffs. May also be a level above a supervisor within high volume administrative/production environments. Makes day-to-day decisions within or for a group/small department. Has some authority for personnel actions. To be a Biopharma Process Development Supervisor typically requires 3-5 years experience in the related area as an individual contributor. Thorough knowledge of functional area and department processes.

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