Quality Assurance

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Opportunities in Boston and Paddington, London

At Vertex, scientific innovation is at the core of everything we do. Our Quality Assurance (QA) teams play an integral role in helping to bring our medicines to the patient communities we serve by ensuring every product is delivered to the highest standard. 

We are relentless in our approach to use science and innovation to do the impossible. At every point in the delivery process, we welcome new ways to innovate and encourage openness, transparency, collaboration and embrace different perspectives.

 

Who we're looking for


At Vertex, we approach QA with a Vertexian mindset. This means we are looking for people who want to operate at the heart of the process – not just the final checkpoint. Our QA team depends on strong communication and cross-functional collaboration skills, values the exchange of ideas and encourages others to think differently. 

We’re not head-down at a lab bench all day. We have a vision, and you need one too. We thrive because we are connected to a real sense of purpose – to help deliver transformative medicines to patients we serve as quickly as we can.

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Sr. Director, Packaging and Labeling Operational Quality

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 will support International global expansion product launches and assessment of product requirements including labelling requirements in local countries/affiliates. 

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Associate Director, Packaging & Labeling, Quality Operations

The Associate Director, Packaging and Labeling, Quality Operations is responsible for the quality oversight of critical components Contract Development and Manufacturing Organizations (CDMOs) for Cell & Genetic Programs through the lifecycle development process. This includes quality oversight for the selection, qualification and routine monitoring of Contract manufacturers and laboratories.

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Medical Device Quality Director – C&GT (Paddington, UK)

Combination Cell Technology Medical Device Quality Director role will be the subject matter expert for Global Medical Device regulations within Cell & Genetic programs.  The role will have broad knowledge of the EU and UK Medical Device regulations as well as international ISO/AAMI standards requirements for implantable medical devices and combination products.

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Why join Vertex?


At Vertex, the world’s most talented and passionate people come together to advance science and transform lives, and in return, we invest in our people so they can accelerate their own careers. We provide a wide range of learning and challenging growth opportunities, and an industry-leading compensation and benefits structure. We are dedicated to fostering the best and most diverse teams possible and take pride in our ability to collaborate seamlessly in tackling the toughest scientific and medical challenges. This investment not only allows our employees to advance their careers, but also enables our teams to make a greater impact on the lives of the patients we serve.
 

Our industry-leading benefits

Our benefits program is designed to support our employees at every stage of their lives, from tuition reimbursement and fertility support to elder care planning. Incredible work deserves incredible rewards. 
 

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Recognized for our efforts

We’ve achieved multiple industry awards for excellence, innovation and being a top employer, including Fortune 100 Best Companies to work for 2023, and Science 2022 Top Employer. Read more about our award recognitions below.

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