Executive Director, Development Quality Lead

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.

Madrigal's medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR-β agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c).

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.

Provides phase-appropriate Quality Assurance leadership for development activities, embedding quality planning and risk management into development execution. Establishes governance for development quality oversight and ensures development documentation is traceable, controlled, and inspection ready. Partners with CMC and clinical supply stakeholders on control strategy evolution, readiness milestones, and tech transfer / scale-up planning. Guides the application of QMS processes (deviations, CAPA, change control) in development contexts and supports efficient progression toward commercialization. Oversees development partners / vendors as applicable and drives issue resolution and compliance readiness.
Key Responsibilities
Development QA Governance & Risk Management
• Define phase-appropriate QA oversight model and governance cadence, ensure readiness milestones and deliverables are clear
• Embed risk management into development execution and ensure documentation expectations and traceability are met
• Produce deliverables such as program quality plans, risk registers, and readiness milestone trackers
QMS Process Oversight (Development)
• Guide deviations / CAPA / change control expectations for development activities, ensure timely, risk-based decisions and closures
• Support tech transfer and scale-up readiness planning with CMC / clinical supply stakeholders
• Produce deliverables such as governance packs, decision logs, and readiness checklists
Partner / Vendor Oversight & Inspection Readiness
• Oversee development partners / vendors as applicable, drive issue resolution and oversight governance
• Maintain inspection readiness plans, evidence packages, and training / standards for development quality
• Produce deliverables such as vendor oversight plans, audit schedules, and inspection-ready evidence indexes
Required Qualifications
• BS+ (Life Science, Engineering, or related)
• 18+ years QA (development / tech ops preferred) with governance and audit support experience
• Demonstrated cross-functional leadership and risk-based judgment
Preferred Qualifications
• Experience in pharmaceutical / biotech development quality and supporting development inspections / submission readiness (preferred)
• Experience overseeing CRO / CMO development partners
Key Competencies
• Development QA governance, phase-appropriate oversight, and readiness milestone management, documentation traceability discipline
• Quality risk management and decision support, deviation / CAPA / change control application in development context
• Partner / vendor oversight and audit readiness planning, issue escalation and follow-through across external networks
• Cross-functional leadership, escalation, and executive-ready risk / decision communication
• Control strategy evolution partnering with CMC and clinical supply, tech transfer / scale-up readiness alignment
• Veeva Vault Quality (eQMS) proficiency to manage development QMS records and inspection-ready traceability

Madrigal's Total Rewards strategy is based on a biotech industry peer group comparator and is inclusive of base pay, bonus and equity. Our equity offers meaningful opportunity allowing our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.
All employees receive equity, which we believe reinforces our ownership culture.


Base salary is determined by several factors including the candidate's qualifications, skills, education, experience, business needs and market demands. As of the date of this posting, a good faith estimate of the current pay scale for this position, applicable to all candidates, is $276,800 - $338,300 per year. We comply with all applicable minimum wage laws.

All full-time employees receive equity, which reinforces our ownership culture and offers meaningful opportunity for our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.


Full-time employees are also eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans. We also offer additional voluntary benefits like supplemental life insurance, legal services, and other offerings. In addition, we offer mental health benefits through our Employee Assistance Program for employees and their family. The company also provides other benefits in accordance with applicable federal, state, and local laws.


We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process. If you need assistance, please contact View email address on click.appcast.io.


Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law.


Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established.


Applications are being accepted on an ongoing basis and can be submitted through our Madrigal Careers site.


Please be aware that we have received reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals' Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal's name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.


Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for or on behalf of Madrigal, we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks. Any questions regarding the legitimacy of job-related contacts can be directed to View email address on click.appcast.io.