Associate Director, Development Quality – OSD

Regulatory Toolkit

Conshohocken (Montgomery County)

On-site

USD 169,000 - 198,000

Full time

14 days+

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Benefits offered by this job

flexible paid time off
medical
dental
vision
life/disability insurance
401(k) offerings
equity ownership

Job summary

Madrigal is seeking a Program QA Leader (Oral) to drive quality strategy across development programs for our MASH portfolio. You will own governance, readiness milestones, and risk management, ensuring inspection-ready documentation and compliance across internal teams and CMOs.

The ideal candidate has BS+ in Life Sciences or Engineering, 10–12 years of development QA experience, and a proven ability to lead cross-functional teams.

Qualifications

  • BS+ Life Sciences / Engineering (or related)
  • 10–12 years QA experience with development-stage oversight
  • Demonstrated cross-functional leadership and risk-based judgment
  • Experience in pharmaceutical / biotech oral product development and clinical supply interfaces (preferred)
  • Experience with external development networks and inspection support

Responsibilities

  • Own quality strategy, governance cadence, and readiness milestones for oral programs
  • Guide application of QMS processes (deviations / CAPA / change control) in development context
  • Produce deliverables such as program quality plans, readiness trackers, and decision / action logs
  • Oversee external vendors / CMOs supporting oral development activities and ensure governance
  • Maintain inspection-ready documentation, narratives, and evidence packages

Skills

QA leadership
Cross-functional leadership
Risk-based judgment
External development networks
Inspection support

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.

Provides modality-focused development QA leadership for oral programs, ensuring phase-appropriate oversight, risk management, and compliant execution across internal teams and external partners. Owns program-level quality strategy, governance cadence, and readiness milestones and ensures development documentation is traceable and inspection-ready. Partners with CMC and clinical supply stakeholders on control strategy evolution, tech transfer readiness, and issue management. Supports efficient progression toward commercialization while maintaining compliance and predictable execution.

Key Responsibilities
Program QA Leadership (Oral)
  • Own quality strategy, governance cadence, and risk register for assigned oral programs, define and track readiness milestones
  • Guide application of QMS processes (deviations / CAPA / change control) in development context and ensure timely closure
  • Produce deliverables such as program quality plans, readiness trackers, and decision / action logs
Partner Oversight & Inspection Readiness
  • Oversee external vendors / CMOs supporting oral development activities as applicable, ensure governance and escalation pathways
  • Maintain inspection-ready documentation, narratives, and evidence packages for program scope
  • Produce deliverables such as vendor governance packs, audit readiness checklists, and inspection evidence indexes
Required Qualifications
  • BS+ Life Sciences / Engineering (or related)
  • 10–12 years QA experience with development-stage oversight
  • Demonstrated cross-functional leadership and risk-based judgment
Preferred Qualifications
  • Experience in pharmaceutical / biotech oral product development and clinical supply interfaces (preferred)
  • Experience with external development networks and inspection support
Key Competencies
  • Development QA governance, phase-appropriate oversight, and readiness milestone management for oral programs
  • Change management (impact assessment, stakeholder mapping, communications, training / SOP readiness, adoption measurement)
  • Partner governance and performance management across CMOs / vendors, inspection readiness evidence discipline
  • Cross-functional leadership, escalation, and executive-ready risk / decision communication
  • Quality risk management, issue triage, and timely action closure across development stakeholders
  • Veeva Vault Quality (eQMS) proficiency to track program quality events, vendor oversight, and readiness documentation

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 $168,737 - $198,073 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.

  • flexible paid time off
  • medical
  • dental
  • vision
  • life/disability insurance
  • 401(k) offerings (i.e., traditional, Roth, and employer match)
  • supplemental life insurance
  • legal services
  • other offerings
  • 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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