Categoria: Healthcare / Pharmaceutical
Luogo di lavoro: Lodi e provincia
Per azienda cliente
Program Manager CDMO
Will be responsible for supporting the execution of drug development and manufacturing programs, ensuring seamless coordination between internal teams and external clients. This role will contribute to operational excellence, risk management, financial accountability, and strategic alignment of projects with business objectives.
Key Responsibilities
Strategic Responsibilities
Support the implementation of program management strategies aligned with business objectives.
Collaborate with cross‑functional teams to align project goals with corporate strategy.
Contribute to process improvement initiatives to enhance operational efficiency.
Operational Responsibilities
Assist in planning, executing, monitoring, and closing projects across drug development and manufacturing.
Ensure adherence to project timelines, regulatory requirements, and quality standards.
Act as a key interface between internal stakeholders, including technical, manufacturing, quality, and regulatory teams.
Track program performance metrics and provide updates to leadership.
People Responsibilities
Work collaboratively with internal teams, ensuring smooth communication and coordination.
Support the team in addressing project‑related challenges and bottlenecks.
Financial Responsibilities
Monitor program costs, assist in budget tracking, and identify opportunities for cost optimization.
Collaborate with finance teams to ensure alignment of program financials with organizational objectives.
Risk Management Responsibilities
Identify potential risks across program timelines, resources, and regulatory compliance.
Support the development and execution of risk mitigation strategies.
Ensure adherence to safety, compliance, and industry practices.
Requisiti
Bachelor’s/ Master’s degree in Life Sciences, Pharmacy, Engineering, or a related field.
Previous experience in program management within a CDMO, pharmaceutical, or biotech industry.
Strong understanding of drug development, manufacturing processes, and regulatory frameworks.
Proven track record of managing complex projects with cross‑functional teams.
Excellent stakeholder management, problem‑solving, and leadership skills.
Proficiency in project management tools and methodologies (PMP certification is a plus).
Strong organizational and project management skills.
Effective stakeholder communication and relationship management.
Ability to coordinate multiple projects and meet tight deadlines.
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