Pharma Project Documentation Lead — Forma & GMP
Listed on 2026-10-12
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Pharmaceutical
Regulatory Compliance Specialist
Scorpion Therapeutics is seeking a Documentation Management Lead to support Design & Construction (D&C) projects in a regulated biopharma environment, with a primary focus on pharmaceutical or biotech facilities. The role will oversee document workflows, ensure compliance, and develop dashboards for project closeout.
Travel up to 100% to client sites, primarily site-based with some remote elements. A Bachelor’s in Engineering, Construction Management, or a related field is required, with
Our group is growing, and we are hiring a Pharma Project Documentation Lead — Forma & GMP in South San Francisco, CA, United States.
The advertised compensation is 120..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Pharma Project Documentation Lead — Forma & GMP role in the description above.
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