Madrigal Pharmaceuticals
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.
Liver Disease β’ NASH β’ Metabolic Disease
51 - 200 employees
π Pharmaceuticals
𧬠Biotechnology
βοΈ Healthcare Insurance
π° $259M Post-IPO Equity on 2022-12
Associate Director - Manufacturing Science and Technology
February 14
Madrigal Pharmaceuticals
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.
Liver Disease β’ NASH β’ Metabolic Disease
51 - 200 employees
π Pharmaceuticals
𧬠Biotechnology
βοΈ Healthcare Insurance
π° $259M Post-IPO Equity on 2022-12
π Description
β’ Responsible for leading the technical strategy and overseeing the implementation of scientific, technological, and operational processes β’ Work closely with cross-functional teams including R&D, Quality Assurance, Regulatory, Engineering, and Operations β’ Ensure that all products are manufactured in compliance with regulatory standards while maintaining operational excellence β’ Serve as the technical expert for Drug Substance and Drug Product manufacturing processes
π― Requirements
β’ BS, MS, or PhD in Biotechnology, Chemical or Pharmaceutical Engineering, or related field β’ 8-10 years of work experience β’ Proven track record of managing large-scale manufacturing operations β’ Experience leading and/or interacting with GMP manufacturing, process validation, and tech transfer teams β’ Ability to communicate effectively across all levels of the organization β’ Deep knowledge of cGMP, FDA regulations, and other global regulatory standards β’ Proficiency in using statistical process control (SPC), Lean, Six Sigma, or other continuous improvement methodologies
ποΈ Benefits
β’ flexible paid time off (PTO) β’ medical, dental, vision, and life and disability insurance
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