Descrizione dell'offerta
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 local pay‑transparency laws.
Additional benefits may include an annual bonus and eligibility to participate in GSK’s share‑based long‑term incentive program, depending on the level of the role. Detailed information on the total benefits package will be provided during the recruitment process. About GSK GSK is a global biopharma company striving 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 through innovative medicines and vaccines across respiratory, immunology, oncology, HIV and infectious disease therapeutic areas. Our culture is ambitious for patients, accountable for impact, and committed to doing the right thing, creating an environment where people can thrive and focus on what matters most.
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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 local pay‑transparency laws.
Additional benefits may include an annual bonus and eligibility to participate in GSK’s share‑based long‑term incentive program, depending on the level of the role. Detailed information on the total benefits package will be provided during the recruitment process. About GSK GSK is a global biopharma company striving 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 through innovative medicines and vaccines across respiratory, immunology, oncology, HIV and infectious disease therapeutic areas. Our culture is ambitious for patients, accountable for impact, and committed to doing the right thing, creating an environment where people can thrive and focus on what matters most.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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