This role will report to the senior manager of Product Development and focus on the design and transfer of implantable cell encapsulation devices for delivering proprietary cells. The successful candidate will join the Process Engineering Team and work closely with Research and Development, Device Quality Control, Device Quality Assurance, Regulatory Affairs, and Manufact

Reporting to the Senior Director of Global Revenue, the Revenue Accounting Senior Manager will play a critical role on Vertex's Global Revenue team as Vertex prepares for the launch of new products. The role will be integral in developing new capabilities and reporting to support additional products and complex estimation processes for gross to net revenue. This role will

Vertex is seeking an experienced senior accounting professional to join our Controllership organization leading the revenue accounting for the Company's Pain product(s). Vertex is preparing for the potential launch and commercialization of an investigational novel selective inhibitor of NaV1.8 in acute pain. Reporting to the Executive Director of Global Revenue Accounting

The Senior Medical Director, T1D (Transplant Immunology/ Endocrinology) will define all aspects of T1D translational strategy and will be accountable for delivering key translational milestones. They will work with cross functional multidisciplinary teams to define overall translational strategy as well as clinical trials strategy, design and execution, and may serve as t

The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with cross functional teams on trial strategy, design, execution, and reporting. In addition to oversight and accountability for the study as a whole, this role will serve as the internal primary Medical Monitor accountable for monitoring the safety of enrolled

The Associate Medical Director will serve as the Medical Lead for Vertex clinical trials in Cystic Fibrosis (CF), working with cross functional multidisciplinary study teams on clinical trial strategy, design and execution and serving as the primary Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned trials. This individual will work on

Vertex Pharmaceuticals is searching for an Associate Medical Director who will be assigned to clinical trials within the Pain Program. You will work as part of multidisciplinary cross functional study teams on clinical trial design and execution and serving as the primary or back up Medical Monitor responsible for monitoring the safety of enrolled subjects on assigned tri

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

The qualified candidate in this role will be managing the newly developed function called the Advanced Manufacturing Engineering under the Global Engineering team. The position provides strategic partnerships with the CMC and Commercial teams to improve, optimize and launch new/existing products at internal and external manufacturing sites. This role will involve in vario

The Sr. Director of Packaging and Labelling Operational Quality will advance compliance oversight for packaging and labelling validation, commercial supply, and product launches in North America and worldwide across the Small Molecule portfolio. The Sr. Director will have a broad role working with stakeholders across Manufacturing, Supply Chain and Regulatory. The role wi

The Director, Cell & Gene Quality, International will support defining the strategy for the international expansion of Cell & Genetic programs. The role will establish the quality risk management plans, work closely with cross functional QA, CMC, External manufacturing, Supply Chain and Commercial teams to ensure QA oversight is maintained. Key activities include develop,

The Associate Director, Modeling & Simulation will combine strong pharmacometric skills with deep biological understanding toindependently determine, plan, and execute M&S analyses in close collaboration with cross functional colleagues within the R&D organization. This incumbent determines, plans, and executes technically challenging analyses b y using state of the art M

Lead the design and execution of experiments, together with the team, to evaluate new medium components and supplements, confirm the cell culture performance. Align with leadership to develop strategic roadmap on continuous medium optimization and phase appropriate medium development and implementation. Manage the medium development team to ensure timely delivery of cell

Responsibility to build and execute the Global Medical strategy for key CF products. Communicate the Global Medical strategy to partner functions and senior leaders 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 partner functions to identify