Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.
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Position Summary
You will lead CMC (Chemistry, Manufacturing and Controls) activities for vaccine development projects in the United States. You will work closely with cross-functional teams including regulatory, clinical, quality, manufacturing and external partners. We value clear decision-making, collaborative problem solving, and hands-on delivery. This role offers growth through complex technical challenges and visible impact on project success, aligned with our mission of uniting science, technology and talent to get ahead of disease together.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Lead development and execution of CMC project plans to support clinical development and regulatory submissions for vaccine candidates.
- Coordinate technical input across quality, manufacturing, analytical development and regulatory to enable timely deliverables.
- Identify, assess and manage CMC risks and mitigation plans that affect project timelines and regulatory acceptance.
- Prepare, review and approve CMC documentation for regulatory filings and meetings with health authorities in the US.
- Represent the CMC voice in cross-functional project meetings and drive decisions to resolve technical or programmatic issues.
- Mentor and coach team members, and support capability building across the project team.
Why You?
If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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