CMC Technical Project Manager (Biopharmaceutical)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
CMC Technical Project Manager (Biopharmaceutical): Providing operational management for CMC development and technical transfer projects with an accent on tactical support, schedule maintenance, and cross-functional coordination. Focus on managing deliverables for biopharmaceutical clients, overseeing CDMO activities, and ensuring alignment between budget, quality, and timelines.
Location: Milan, Italy
Company
is a global management consulting group specializing in strategic consulting and product development for the life sciences and healthcare industries.
What you will do
- Provide tactical support for day-to-day CMC project activities, including meeting minutes, action tracking, and decision logging.
- Build and maintain detailed predecessor-driven project schedules and Gantt charts using tools like Planisware.
- Coordinate across functional areas such as process development, analytical, formulation, quality, and supply chain.
- Prepare project management deliverables, including reports, dashboards, and routine updates on budget and risk.
- Manage and oversee outsourced development and manufacturing activities with CDMOs.
- Ensure project schedules remain aligned with regulatory submissions and health authority interactions.
Requirements
- At least 2 years of experience in the biopharmaceutical industry, with a minimum of 1 year in project management.
- BS, MS, or PhD in a scientific or engineering discipline (e.g., Chemistry, Biochemistry, Pharmaceutical Sciences).
- Proficiency in Planisware.
- Experience working with CDMOs to support outsourced manufacturing activities.
- Fluent and articulate communication in English (written and spoken).
- Ability to engage in technical and scientific discussions.
Nice to have
- Broad understanding of CMC for small molecules, biologics, or vaccines.
- Formal project management training or PMP certification.
- Understanding of cGXP guidelines and regulatory requirements.
- Knowledge of the product development lifecycle and pharmaceutical manufacturing operations.
Culture & Benefits
- Entrepreneurial journey with a focus on innovation, teamwork, and excellence.
- Professional development support through guidance and real-time feedback.
- Continuous learning and development opportunities.
- Commitment to employee wellbeing and an equal opportunity work environment.
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