Scorpion Therapeutics is seeking a dedicated Document Management Lead for Clinical Development to own the end-to-end lifecycle of controlled documents within the eQMS, ensuring compliance and timely delivery. You will partner with Clinical Ops, QA, Regulatory Affairs, and other functions to manage workflows, audits, and inspections, maintain metadata and document integrity, and drive process improvements.
This role is in California with in-office requirements and 5+ years in pharma/biotech
#J-18808-LjbffrLead, Clinical Quality Documents & eQMS in los angeles at Unknown Company
This position is listed as full time and onsite.