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The role involves overseeing outsourced microbiology testing, ensuring GMP compliance, supporting contamination control strategies, and authoring relevant regulatory documents.

Lead Quality Control activities for a clinical-stage autologous cell therapy program, ensuring compliance and operational readiness while establishing QC strategies and overseeing external partners.

The role involves managing document control and training processes to ensure compliance with regulations. Responsibilities include overseeing GxP document lifecycle and training programs, supporting audits, and collaborating with stakeholders to implement systems and processes.

Obsidian Therapeutics seeks candidates for its Talent Community for dynamic roles in engineering precision cell and gene therapies, despite not listing specific positions.