13 ago - Italia
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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. GSK's 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. We foster a culture ambitious for patients, accountable for impact, and committed to doing the right thing, accelerating assets that meet patients' needs and have the highest probability of success. United, we are science, technology, and talent working together to get ahead of disease.
Position Summary
You will lead CMC (Chemistry, Manufacturing and Controls) activities for vaccine development projects in the United States, working closely with regulatory, clinical, quality, manufacturing and external partners. This role requires clear decision‐making, collaborative problem solving, and hands‐on delivery, offering growth through complex technical challenges and a visible impact on project success.
Responsibilities
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.
Compensation & Benefits
Salary ranges (annual gross base) vary by location:
Poland – PLN 306,750 – 511,250
Italy – EUR 57,300 – 95,500
Belgium – EUR 90,000 – 150,000
Other applicable markets – respective ranges displayed according to
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