обновлено 4 дня назад
Senior CMC Global Project Manager (Biotech)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior CMC Global Project Manager (Biotech): Developing and executing integrated CMC roadmaps and project plans for pharmaceutical assets with an accent on cross-functional drug development, regulatory delivery, budgets, resources, and risk management. Focus on coordinating CMC subteams, managing complex interdependencies and governance decisions, and delivering milestones on time and within budget.
Location: Paris, France; hybrid work
Company
is a global biopharmaceutical company developing medicines in Oncology, Rare Disease, and Neuroscience.
What you will do
- Develop, maintain, and execute strategic CMC roadmaps and integrated project plans across asset functions.
- Lead cross-functional CMC subteams and serve as the central operational contact for project and Asset Team members.
- Coordinate deliverables, milestones, critical paths, dependencies, decisions, and governance activities.
- Manage project risks, issues, contingencies, scope changes, budgets, resources, and external costs.
- Track project performance through metrics, reporting, lessons learned, benchmarking, and data-driven analysis.
- Support process improvements and transversal initiatives across Asset Operations, CMC, and GPO.
Requirements
- 8–10+ years of experience in the pharmaceutical or biotech industry, including CMC development and project management.
- Experience leading operations in cross-functional drug development teams across relevant development stages.
- Strong leadership, stakeholder management, communication, facilitation, prioritization, problem-solving, and decision-making skills.
- Experience managing project budgets, resources, risks, timelines, and cross-functional deliverables.
- Strong proficiency with Microsoft Office, Microsoft Project, and other project management tools.
- English and French required; bachelor’s degree in Science required.
Nice to have
- Experience with US or EU pharmaceutical regulations.
- Experience in CMC, clinical, preclinical, or regulatory affairs.
- Project management certification, PhD, or PharmD.
Culture & Benefits
- Collaborative, cross-functional environment focused on patient impact and scientific innovation.
- Human-centric leadership and an inclusive workplace supporting individual development.
- Global organization with teams operating across more than 40 countries.
- Quality management and regulatory compliance are integrated into project execution.
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