The Senior Director, Quality is responsible for the oversight of Product Quality Leads for all Vertex Small Molecule programs, development and commercial. As the group leader, the Sr. Director is responsible for supporting commercialization, filing/approval, launch, and post approval lifecycle management. This role will partner closely with Quality and business stakeholde

Lead and ensure successful development and implementation of the commercialization (midterm) and portfolio (long term) strategies including brand development, competitive strategy, go to market/launch, and lifecycle decisions for future launches. Execute in close partnership with the Regions, Market Access, Regulatory and Commercial Manufacturing. Deliver foundational ins

Vertex is seeking a talented individual to join the Engineering and Materials Science group in Boston, MA. The successful candidate will be a highly productive, results oriented individual, able to multi task and generate and implement original ideas that contribute to the successful development and scale up of drug substance processes, including crystallizations. Strong

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

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

1. Develops and fosters effective and trusting relationships with Thought Leaders and identifies and engages other appropriate (allied) HCPs and other stakeholders involved in clinical practice decision making with regards to managing conditions associated with pain, resulting in scientific engagement with a large network of stakeholders involved in affecting care of pati

Acts as main point of contact for CDMO(s), building and maintaining strategic relationships within the CDMO organization. Responsible for driving execution of Drug Product production plans Provide operational oversight and troubleshooting support to ensure all deliverables meet or exceed Vertex requirements (including but not limited to successful execution of manufacturi

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

The Analytical and Purification Principal Research Associate will lead the small molecule chiral purification platform within the Medicinal Chemistry group. The individual will propose and develop improvements in the purification workflow along with implementing new software and hardware technologies for high throughput separations. In addition, the successful applicant w

This position is responsible for establishing and managing a global occupational and environmental toxicology program. The individual will be required to provide stewardship and support for Vertex's project portfolio. The individual will be part of the global environmental health and safety (EHS) team responsible for setting standards, developing culture and programs esta

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

P lay a critical role in setting up in house chargeback function , working cross functionally with 3 PL, Trade & Distribution, Accounting, and DTE, etc. to develop policies, efficient processes, system requirements, and department al SOPs . Partner with Government Pricing & Programs , Contract Operations , Payer Accounts and Legal, etc. to p rovide key insights during con

The Senior Director, Quality GLP, Biomarkers and Research has overall accountability for strategic leadership and oversight of the end to end quality assurance strategy for proactive, risk informed, and sustainable quality oversight and compliance with regulatory expectations across Vertex processes for clinical evidence generation and product vigilance Key Duties and Res

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria

Establishes meaningful and professional relationships within key accounts across multiple layers of the hospital system (key hospital medical and administrative staff, pharmacies, formulary decision makers and KTLs) Develops and maintains expertise on the product's clinical attributes and patient unmet need and educates healthcare professionals on product use in appropria