
A biotechnology firm in Redwood City is seeking an experienced Associate Director/Director of CMC Regulatory Affairs. This position focuses on developing regulatory strategies, managing documentation for regulatory submissions, and collaborating across departments to ensure compliance. Candidates should have an advanced degree and at least 8 years of experience in CMC regulatory affairs, along with proficiency in FDA interactions and a strong understanding of GMP standards. The role offers a competitive compensation package and extensive benefits.
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