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The Director, Manufacturing Technical Services, Quality Assurace is responsible for the quality oversight of Contract Manufacturing Organizations (CMOs) and Contract Test Labs (CTOs) for Cell & Genetic Programs through the lifecycle development process. This includes quality oversight for the selection, qualification and routine monitoring of Contract manufacturers and la
Posted Today
The Senior GCP Operational Quality Manager conducts quality assurance oversight and management activities of clinical trial operations to ensure Vertex trials are conducted in accordance with Good Clinical Practice (GCP) guidelines, applicable regulations, protocols and Vertex policies and procedures. These activities include the development and execution of study level a
Posted Today
The Formulation Research Scientist will work with other scientists dedicated to advancing drug candidates from exploratory development through commercial line extension in a Quality by Design (QbD) environment using lab based and computational tools to design and select dosage forms and manufacturing process. Key Duties and Responsibilities Develop dosage forms for clinic
Posted Today
As a key member of the Corporate/North American accounting department, the General Ledger Senior Accountant II partners with members of the accounting and finance departments as well as teams across other departments throughout the Company. The position provides exposure to key accounting and reporting areas and offers development opportunities that can lead to advanced r
Posted Today
Plan packaging based off study design. This includes packaging design to be used Bottles vs blisters and qty of supplies to produce Plan production activities Following packaging completion, responsible for determine inventory release timing and stocking of depots taking into consideration the following but not limited to expiry, countries, key study milestone dates, numb
Posted Today
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
Posted 1 day ago
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
Posted 1 day ago
Lead the tactical execution of design planning, informing the development of scalable, effective distribution strategies to serve short and long term expectations while considering financial impacts and patient/customer experience Collaborate and drive alignment across key stakeholders on distribution and channel strategy development; apply subject matter expertise to max
Posted 4 days ago
Works cross functionally to ensure an integrated brand strategy that includes patient services, patient educators, patient advocacy, and communications. Ensures that the brand strategy is translated with an effective launch tactical plan for patients and caregivers Engages with the patient communities, both those with sickle cell disease (SCD) and transfusion dependent th
Posted 4 days ago
The individual in this role will support the delivery of the patient and caregiver marketing strategy and tactical plan for our first genetic therapy for hemoglobinothapies (sickle cell disease and beta thalassemia), Casgevy. The Senior Marketing Manager will be responsible for overseeing development of brand and unbranded marketing tactics for the Sickle Cell disease ind
Posted 4 days ago
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
Posted 4 days ago
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
Posted Today
Our department is a highly collaborative collection of groups consisting of biology, engineering, modeling and simulation, and prototyping, centered around developing cutting edge transformative cell and gene delivery platforms. In this position the intern will support routine analytical testing and material characterization, in addition to assisting with fixture design,
Posted 11 days ago
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
Posted Today
The Platform & Enabling Technologies group within VCGT Device Analytical Development is focused on proactively identifying platform technologies to improve Device characterization and process understanding. The Principal Scientist will lead a team of scientists to search out new technologies, obtain proof of concept for our specific application, and develop an implementat
Posted 11 days ago
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