Regulatory CMC Technical Writer - Cell Therapy

A leading biopharmaceutical company is looking for a Technical Writer and Document Specialist to provide CMC documentation and support regulatory strategy for their cell therapy clinical portfolio. Responsibilities include authoring scientific content for regulatory submissions, managing project timelines, and collaborating with SMEs across the organization. Candidates must have a relevant degree and cell therapy CMC experience, with proficiency in Microsoft Office and regulatory Documentum software.

This role offers a dynamic work environment with opportunities for professional growth.
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