PpbCategoria: /b Healthcare / Pharmaceutical /p pbLuogo di lavoro: /b Lodi e provincia /p pPer azienda cliente /p h3Program Manager CDMO /h3 pWill 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. /p h3Key Responsibilities /h3 h3Strategic Responsibilities /h3 ul liSupport the implementation of program management strategies aligned with business objectives. /li liCollaborate with cross‑functional teams to align project goals with corporate strategy. /li liContribute to process improvement initiatives to enhance operational efficiency. /li /ul h3Operational Responsibilities /h3 ul liAssist in planning, executing, monitoring, and closing projects across drug development and manufacturing. /li liEnsure adherence to project timelines, regulatory requirements, and quality standards. /li liAct as a key interface between internal stakeholders, including technical, manufacturing, quality, and regulatory teams. /li liTrack program performance metrics and provide updates to leadership. /li /ul h3People Responsibilities /h3 ul liWork collaboratively with internal teams, ensuring smooth communication and coordination. /li liSupport the team in addressing project‑related challenges and bottlenecks. /li /ul h3Financial Responsibilities /h3 ul liMonitor program costs, assist in budget tracking, and identify opportunities for cost optimization. /li liCollaborate with finance teams to ensure alignment of program financials with organizational objectives. /li /ul h3Risk Management Responsibilities /h3 ul liIdentify potential risks across program timelines, resources, and regulatory compliance. /li liSupport the development and execution of risk mitigation strategies. /li liEnsure adherence to safety, compliance, and industry practices. /li /ul h3Requisiti /h3 ul liBachelor’s/ Master’s degree in Life Sciences, Pharmacy, Engineering, or a related field. /li liPrevious experience in program management within a CDMO, pharmaceutical, or biotech industry. /li liStrong understanding of drug development, manufacturing processes, and regulatory frameworks. /li liProven track record of managing complex projects with cross‑functional teams. /li liExcellent stakeholder management, problem‑solving, and leadership skills. /li liProficiency in project management tools and methodologies (PMP certification is a plus). /li liStrong organizational and project management skills. /li liEffective stakeholder communication and relationship management. /li liAbility to coordinate multiple projects and meet tight deadlines. /li /ul /p #J-18808-Ljbffr