Program Manager CDMO

Azienda

Chemical Pharmaceutical Company (API), located in Lodi

Offerta

The 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.

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.

Competenze ed esperienza

• Bachelor's/ Master's degree in Life Sciences, Pharmacy, Engineering, or a related field.
• 3-6 years of 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).
• Excellent communication, interpersonal, and leadership skills.
• Collaborates with other departments, including Research and Development, Manufacturing, and Regulatory Affairs, to ensure a unified approach to quality.

Completa l'offerta

Great career opportunity