Madrigal Pharmaceuticals
Pharmaceuticals • Biotechnology • Healthcare Insurance
Madrigal Pharmaceuticals is a biopharmaceutical company focused on developing novel therapeutics for nonalcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). The company achieved a significant milestone with the accelerated FDA approval of its first therapy for adults with NASH with moderate to advanced liver fibrosis. Madrigal is actively conducting a Phase 3 trial for the treatment of NASH with compensated cirrhosis. The company is dedicated to improving care for patients with NASH/MASH through its ambitious research programs and therapeutic developments.
51 - 200 employees
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $259M Post-IPO Equity on 2022-12
Associate Director - Manufacturing Science and Technology
Job not on LinkedIn
February 14
Madrigal Pharmaceuticals
Pharmaceuticals • Biotechnology • Healthcare Insurance
Madrigal Pharmaceuticals is a biopharmaceutical company focused on developing novel therapeutics for nonalcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). The company achieved a significant milestone with the accelerated FDA approval of its first therapy for adults with NASH with moderate to advanced liver fibrosis. Madrigal is actively conducting a Phase 3 trial for the treatment of NASH with compensated cirrhosis. The company is dedicated to improving care for patients with NASH/MASH through its ambitious research programs and therapeutic developments.
51 - 200 employees
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $259M Post-IPO Equity on 2022-12
📋 Description
• Responsible for leading the technical strategy and overseeing the implementation of scientific, technological, and operational processes • Work closely with cross-functional teams including R&D, Quality Assurance, Regulatory, Engineering, and Operations • Ensure that all products are manufactured in compliance with regulatory standards while maintaining operational excellence • Serve as the technical expert for Drug Substance and Drug Product manufacturing processes
🎯 Requirements
• BS, MS, or PhD in Biotechnology, Chemical or Pharmaceutical Engineering, or related field • 8-10 years of work experience • Proven track record of managing large-scale manufacturing operations • Experience leading and/or interacting with GMP manufacturing, process validation, and tech transfer teams • Ability to communicate effectively across all levels of the organization • Deep knowledge of cGMP, FDA regulations, and other global regulatory standards • Proficiency in using statistical process control (SPC), Lean, Six Sigma, or other continuous improvement methodologies
🏖️ Benefits
• flexible paid time off (PTO) • medical, dental, vision, and life and disability insurance
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