The Senior Manager of GMP Inspection Readiness role is responsible for managing real time inspection readiness activities supporting GMP quality. The role requires the ability adapt to new and multiple projects, effectively ensuring alignment with corporate goals and compliance with all regulatory requirements. The role is responsible to provide technical expertise and pr

Lead the drafting/development of key abstracts, posters, congress presentations, and manuscripts Coordinate with cross functional teams and key stakeholders to achieve publication objectives Manage publication development timelines and content development associated with abstracts, posters, oral presentations, and manuscripts Responsible for the execution of the global pu

The Sr. Principal Oracle EBS Project Costing Lead will be a key technical resource in ensuring the planning and delivery of key commercial off the shelf (COTS) and a wide range of custom solutions in support of their business partners in Accounting and Finance. The Business Engagement & Technology Senior Principal Analyst for Accounting will partner with business leadersh

As a key Team Manager and leader in the Strategic Sourcing function, the Executive Director, Manufacturing & Supply Strategic Sourcing leader is responsible for elevating global business partnerships with an enterprise lens while focusing on enabling business outcomes and integrating relevant category strategies. This role will lead multiple direct reports that have teams

Participate in the design, development and implementation of novel delivery strategies for genome editing technologies. Generate custom lipid based formulations and targeting molecules to optimize LNP delivery for various tissues. Develop and execute LC MS based, molecular, cell based assays to test novel gene editing tools and candidate therapeutic assets. Collaborate wi

Vertex pharmaceuticals is seeking a research scientist to join our analytical development team in cell and gene therapy organization. This position is expected to provide key technical expertise in developing molecular based assays to support process development, product characterization and product release for our C> pipelines. Our team is seeking experienced, innovati

The Sr. Quality Manager is an advanced technical resource in the principles and application of quality assurance and compliance. The Sr. Quality Manager coordinates or executes activities on multiple complex projects and takes a role in the design and execution of new projects , effectively ensuring alignment with corporate goals and compliance with all regulatory require

Promote and support adoption of inclusive practices; working with the ID&E team to establish key initiatives that are tailored to advance Vertex wide ID&E goals while also supporting functional and regional needs. Support the development and rollout of educational workshops, thought leader/speaker programs, and tools that support ID&E focus areas, working in partnership w

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

We are seeking an accomplished and innovative scientist to lead a drug discovery team within the medicinal chemistry group at the Boston research site. This individual will lead, motivate, and develop a team of approximately 10 15 highly skilled PhD/MS/BS chemists through early hit discovery, lead optimization, and drug candidate identification. The leader will have deep

Major contributor and driver to the company safety risk management, signal detection, benefit/risk assessments, and post marketing regulatory research strategies Expected to research the epidemiology of specific disease areas and events of interest, lead evaluation of data sources and data collection approaches, apply subject matter expertise in the design of observationa

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

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

Acts as the main point of contact for CDMO(s) including the leader of the CDMO VPT/working team. Responsible for driving execution of commercial and late stage/launch 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 manufacturing

Responsible for Global payer strategic planning to support value and access optimization for chronic indications for our Pain portfolio Lead development of Market Access strategies and core Global P&R deliverables operating within the cross functional, cross regional commercialization process Responsible for Global payer strategic planning to support value and access opti