Vertex seeks a talented scientist to join the Vertex Cell and Genetic Therapies (VCGT) stem cell research group in Boston, MA. The group's mission is to discover and actualize the next generation of cell therapies for diabetes. We are looking for a candidate with a background in stem cell biology and metabolism, interested in working at the intersection of cell therapy an

Ability to empower teams and individuals and hold them accountable Executive presence, strong business acumen, ability to navigate ambiguity and manage complexity Exhibits intellectual curiosity and integrity and has a strong passion for innovation Ability to think strategically and effectively assess, plan, and prepare recommendations Highly developed interpersonal skill

The Associate Director, Biomarker Operational Quality will provide biomarker quality leadership and oversight across GxPs related to research and development, implementation into clinical trials and potential commercialization of clinical biomarkers into IVDs. This leader will collaborate with business partners and GCP Operational Quality to drive quality outcomes and ope

As the Director of Omnichannel Analytics , you will be responsible for shaping our data analytics strategy, budget planning by therapy area, ensuring the appropriate integrated omnichannel promotion strategy, and collaborating with business unit teams to derive actionable insights to improve customer experiences and business outcomes. This position is a hybrid role which

Through internal audits the Internal Audit Manager will identify risk areas, evaluate business process controls and complete test plans. Additionally, this role will provide recommendations to improve the effectiveness and efficiency of operations and business systems. This role will also participate in ensuring that the yearly internal control review is brought to fruiti

Leads team development and harmonization by utilizing exceptional leadership and team building skills. Leads creation of team goals and works by example, fostering collaboration across team. Collaborates closely with Finance to communicate anticipated budget changes and projections. Provide quarterly projections to Leadership to ensure alignment on anticipated risks and a

The Director, Regulatory CMC (Chemistry Manufacturing Controls) is responsible for the development and implementation of post approval global regulatory CMC strategies for a marketed cell and gene therapy product. This role provides regulatory guidance to various cross functional teams to ensure all applicable global regulatory requirements are considered and appropriatel

Vertex's Data, Technology and Engineering (DTE) team is seeking a Manufacturing and Supply Chain (MSC) Technology Portfolio Manager to join our Project Management and Strategic Operations group. Project Management and Strategic Operations is charged with streamlining and simplifying the work of our data and technology teams and ensuring the successful deployment of new te

Provides comprehensive expertise and guidance in the Therapeutic Area and Vertex drugs Develops and maintains professional relationships with local Health Care Professionals, and with local Professional Societies and Patient Advocacy groups. Establishes relationships with Thought Leaders to expand research opportunities for Vertex and develops, at local level, advisory, c

Authors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports, investigator's brochures, documents to support meetings with regulatory agencies, and sections of marketing authorization applications) in partnership with key stakeholders Serves as the lead Medical Writing Scientist for complex or pivotal clinical studies for multiple

The Executive Director, Pain Global Strategy will have global responsibility to build the Global Medical strategy for Pain assets. Communicate the Global Medical strategy to partner functions for further strategic and tactical guidance. Execute the Global components of the medical strategy plan. Partner with Clinical Development, HEOR, RWE, Regional Medical Affairs and pa

CMC Project Leadership Partners with Biopharmaceutical Sciences LT members, and CMC PLs to ensure all projects have integrated CMC development plans, aligned with Disease Area Team's strategic program goals and objectives Leads a team of dedicated CMC Project Leaders, each accountable for ensuring the integrated development and on schedule execution of one or more CMC Pro

The Senior Quality Specialist is recognized as an expert internally in the principles and application of quality assurance and compliance. The Senior Quality Specialist coordinates GMP activities in support of clinical and commercial Drug Product manufacturing and disposition. This is an on site position on the 2nd shift. KEY DUTIES AND RESPONSIBILITIES Review batch data,

Maintain a high level of productivity in the laboratory setting Develops and executes clear synthetic routes using state of the art synthetic methodologies Primarily responsible for executing organic syntheses in a timely, efficient, and independent manner Create and interpret SAR with a clear understanding of the biological data Organize and triage efforts to stay consis

Oversee material requirements and lead the device raw material planning process for the providence, RI site for BOM and non BOM materials. Partner with CMC, Procurement and Strategic Sourcing to ensure supply and solve supplier and materials related issues. Manage direct and indirect materials for manufacturing activities, as well as materials for packaging/labeling and s