Director Quality Assurance - FvP

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH.

Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration. To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.

Position Summary Serves as the Swissmedic-recognized Fachtechnisch verantwortliche Person (FvP) and sole named responsible person on the company’s Swiss license, accountable for establishing a robust local Swiss Quality System and for leading the acquisition and ongoing maintenance of the Pharmaceutical Establishment License (PEL). Ensures end-to-end compliance with Swiss and EU GMP/GDP and enables local licensed operations (as applicable) including importation, batch certification/release, distribution oversight, and product control. Acts as a critical interface between global manufacturing operations and the company’s broader corporate and financial structure, actively shaping the operating and control model that underpins the Switzerland-based IP framework, including support for IP establishment/transfer and the legal/operational substance required for Switzerland to act as IP holder. Ensures manufacturing oversight, quality governance, and supply chain controls remain aligned to the conditions necessary to sustain the Swiss entity’s role, and influences decisions on manufacturing footprint, governance model, and quality system design to protect the integrity, defensibility, and continuity of the IP structure. Concurrently retains global quality oversight and governance for API manufacturing, with particular emphasis on uninterrupted US API supply, leveraging internal and external resources for execution while maintaining ultimate FvP accountability and decision authority on Swiss QMS design, compliance strategy, and batch certification (as applicable).

Key Responsibilities Swiss Quality System, PEL & Swissmedic Interface

• Design, implement, and maintain the Swiss QMS aligned with Swissmedic, EU GMP/GDP, and global Quality/Compliance standards
• Lead PEL strategy and execution: Prepare, submit, defend, and maintain the Swiss Pharmaceutical Establishment License (including renewals/variations)
• Serve as primary Swissmedic contact for inspections, correspondence, and regulatory interactions; ensure timely, accurate responses and commitments
• Ensure all authorized activities are performed in compliance with PEL conditions and applicable Swiss regulatory requirements

Operational GMP/GDP Oversight & Release Accountability

• Provide global quality oversight and governance for API manufacturing activities, ensuring appropriate control, compliance, and continuity of supply.
• Perform and/or oversee batch certification/release activities as applicable under Swiss/EU requirements; ensure compliant, inspection-ready release decisions
• Review and approve key manufacturing/testing/distribution documentation required to support Swiss and/or EU market supply
• Oversee GDP-compliant distribution in Switzerland, including qualification and governance of 3PL/warehousing providers
• Ensure temperature monitoring, excursion handling, deviation management, and product integrity controls across the end-to-end supply chain

Global API Quality Governance & Strategic Cross-Functional Leadership

• Provide global quality oversight and governance for API manufacturing to ensure control, regulatory compliance, and continuity of supply (including US-market supply focus as applicable)
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