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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Senior Director - GLP, Biomarkers and Research Quality

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • An M.S. or equivalent degree and 10 or more years of relevant work experience, or a B.S. in a scientific or allied health field or equivalent degree and 15 or more years of relevant work experience, or a relevant comparable background.

Responsibilities

  • Serve as a strategic partner to functional leaders across product modalities responsible for Research, including non-regulated and GLP work, Biomarker Development, and Diagnostics, to assure appropriate quality and compliance oversight of processes and systems supporting program delivery and the rigor and integrity of associated data.
  • Define strategy for, and oversee tactical execution of, the strategic plan by direct reports to provide oversight of research, assay development supporting pre-clinical and clinical research, GLP animal studies, in vitro diagnostic development, and all R&D vendors. Ensure operational quality activities are risk-informed and ensure the integrity of data submitted to regulatory authorities and in external forums.
  • Ensure key internal and external research and pre-clinical studies comply with good scientific practices, good laboratory practices, Vertex policies and procedures, and relevant local, regional, and international requirements.
  • Lead an operational quality team responsible for identifying and anticipating potential compliance issues that may impact business goals, and developing and implementing pragmatic, effective methods for improvement and resolution.
  • Oversee timely and appropriate identification, remediation, and escalation of quality issues in Research, GLP, Biomarker, IVD, and vendor governance-related activities across Vertex.
  • Provide periodic updates to functional leaders across Research, Biomarker Development, and Diagnostics on the overall health of Research, GLP, Biomarker, and IVD development-related processes and systems.
  • Oversee timely and effective communication of summary trends and other insights on quality of delivery in research, preclinical, biomarker, IVD work, and vendor performance to relevant business and quality leaders and forums.
  • Oversee inspection-readiness activities in collaboration with business and Quality Assurance partners for research, GLP, biomarkers, and IVD development activities.
  • Chair relevant operational governance meetings, such as QLT.
  • Serve as the R&D Quality lead and oversee and guide staff participating in strategic cross-functional initiatives, such as Research Ethics and TPRM, to improve quality, data integrity, and compliance with regulatory requirements and standards, ensuring an aligned Quality point of view is represented.
  • Maintain an in-depth understanding of business principles, industry dynamics, the regulatory environment, market trends, and operational details related to Research, GLP, Biomarker, and IVD activities.
  • Drive and oversee implementation of new and evolving regulatory requirements related to areas of responsibility.
  • Lead and/or participate in industry forums and external initiatives related to areas of responsibility to influence policy development concerning oversight of these activities, aligned with functional leadership and Vertex interests.
  • Provide strategic direction, oversight, coaching, and mentoring to direct reports.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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