Precision Point seeks a Regulatory Affairs CMC Consultant to lead CMC authoring, strategy, and lifecycle management for a biologics pipeline. This hands-on role requires setting regulatory strategy and performing technical writing without a team. You will report to the RA CMC Executive Director and collaborate with Analytics, Quality, Manufacturing, and external CMOs to ensure submission readiness and inspection-ready documentation.

Also on the board Same function, level within a rung

Level

Senior

Location

Los Angeles, CA

Occupation

Regulatory Affairs Specialists

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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