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Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our…
Coordinates biopharma packaging projects, manages orders and documentation in ERP systems, and ensures regulatory compliance for life-saving therapies.
Review batch records, approve investigations, and ensure GxP compliance for biopharma manufacturing, shaping quality systems for clinical and commercial products.
Perform real-time GMP quality assurance for biopharma manufacturing, including floor oversight, batch record review, AQL inspections, and issue resolution to ensure regulatory compliance and patient safety.
Design, optimize, and maintain pharmaceutical fill-finish equipment; troubleshoot issues and lead validation to ensure compliant, efficient production.
Oversee custom drug-product projects for biopharma clients, coordinating timelines, budgets, and cross-functional teams to deliver therapies on time and within scope.
Coordinates review and approval of GMP documents using an electronic system, manages archival, and interfaces with authors to meet timelines in a biopharma services role.
Performs environmental monitoring and testing of clean utilities in a cGMP biopharma facility, including gowning, water systems, and plate reads.
Design, implement, and maintain a global enterprise network using Cisco technologies, SD-WAN, and advanced routing/switching to ensure high availability and security across multiple continents.
Lead global tax strategy and compliance for a biopharma services company, optimizing rates and cash flow while managing filings, audits, and transfer pricing.
Monitors aseptic manufacturing processes in cleanroom environments to ensure compliance with quality standards, documenting behaviors and escalating deviations to maintain product safety and patient outcomes.
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