Visium Resources has been asked to identify qualified candidates for a full time position as a Senior CQV Project Manager. Candidate will travel between facilities across the US. The preferred location can include any of the following - North Carolina, Colorado, Indianapolis, Chicago, Philadelphia, Boston, San Diego / LA / Orange County (SoCal).
We are seeking an experienced Senior CQV Project Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects and operational initiatives. This individual will oversee cross-functional CQV execution for GMP-regulated facilities, utilities, equipment, automation systems, and manufacturing processes while ensuring compliance with FDA, cGMP, and global regulatory standards.
The ideal candidate will possess strong pharmaceutical project leadership experience within biotech, sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison between engineering, quality, validation, manufacturing, and external vendors. This role requires the ability to manage project schedules, budgets, risks, resources, and validation deliverables in support of facility expansions, new product introductions, and operational readiness initiatives.
Key Success Criteria
Key Responsibilities
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