Director, Quality – New Product Development Lead

Madrigal Pharmaceuticals

Conshohocken (Montgomery County)

On-site

USD 212,000 - 240,000

Full time

14 days+
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Benefits offered by this job

Equity
Bonus

Job summary

Madrigal Pharmaceuticals is seeking a senior QA leader to oversee development quality strategy and governance across the portfolio. This role partners with CMC and clinical teams to embed risk management early and enable smooth progression toward commercialization while ensuring audit-ready documentation.

The candidate will lead phase-appropriate QMS implementation, vendor oversight, and continuous improvement initiatives to increase predictability and right-first-time outcomes across multiple

Qualifications

  • BS+ Life Sciences or Engineering (or related) degree.
  • 12–15 years QA experience with significant portfolio leadership.
  • Demonstrated people leadership and executive stakeholder influence.

Responsibilities

  • Define development quality operating model, governance forums, and performance metrics.
  • Prioritize portfolio support and mitigate risks with options.
  • Produce deliverables such as portfolio dashboards, governance calendars, and risk briefs.
  • Ensure vendor oversight, audits, issue management, and readiness deliverables.
  • Maintain readiness for development inspections and submission support.
  • Sponsor continuous improvement to improve cycle time and documentation.

Skills

People leadership
Executive stakeholder influence
QA portfolio management

Education

BS+ Life Sciences / Engineering (or related)

Tools

Veeva Vault Quality (eQMS)

Job description

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.

Leads development quality strategy and execution across the new product development portfolio, ensuring phase-appropriate controls and consistent governance across programs and modalities. Establishes operating model expectations, standards, and performance cadences for development QA delivery. Partners with CMC and clinical supply leaders to embed quality risk management early, align readiness milestones, and enable efficient progression toward commercialization. Sets partner / vendor oversight standards and ensures inspection readiness through controlled documentation and audit-ready narratives. Sponsors continuous improvement to increase predictability, throughput, and right-first-time documentation.

Key Responsibilities
Portfolio Leadership & Operating Model
  • Define development quality operating model, governance forums, and performance metrics, ensure consistent decision quality across programs
  • Prioritize portfolio support and elevate resource, timeline, and quality risks with mitigation options
  • Produce deliverables such as portfolio dashboards, governance calendars, and resourcing / risk briefs
Development Oversight & Partner Governance
  • Ensure phase-appropriate QMS application and documentation traceability across programs and external partners
  • Set expectations for vendor oversight, audits, issue management, and readiness deliverables
  • Produce deliverables such as vendor oversight standards, audit strategies, and readiness playbooks
Inspection Readiness & Continuous Improvement
  • Maintain readiness for development inspections and submission support, ensure narratives and evidence are current and retrievable
  • Sponsor CI initiatives to improve cycle time, RFT documentation, and predictable execution across the portfolio
  • Produce deliverables such as inspection readiness plans, evidence indexes, and CI roadmaps / benefits trackers
Required Qualifications
  • BS+ Life Sciences / Engineering (or related)
  • 12–15 years QA experience with significant development portfolio leadership experience
  • Demonstrated people leadership and executive stakeholder influence
Preferred Qualifications
  • Experience in pharmaceutical / biotech across multiple modalities and external development networks (preferred)
  • Experience supporting inspections and major submissions / filings readiness
Key Competencies
  • Portfolio leadership, operating model design, and governance discipline, prioritization, resourcing, and performance cadence ownership
  • Cross-functional leadership, escalation, and executive-ready risk / decision communication
  • Partner governance and performance management across external development networks, audit / inspection readiness planning
  • Quality risk management, phase-appropriate QMS application, and readiness milestone governance across programs
  • Change management (stakeholder mapping, communications, training / standardization readiness, adoption measurement) and continuous improvement sponsorship
  • Veeva Vault Quality (eQMS) proficiency to enable portfolio governance visibility and inspection-ready documentation control

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 $211,591 - $240,461 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 HR@madrigalpharma.com.

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.

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