AbbVie MES Program Manager at AbbVie responsible for managing large global projects across manufacturing and technical disciplines. Leads cross-functional teams to ensure successful tech transfer, commercialization, and capacity strategy.
Responsibilities
•Assemble and lead matrixed cross-functional teams comprised of scientist and engineers responsible for all operational aspects of process development, manufacturing, quality assurance and quality control spanning multiple sites
•Implement site transfers, new indications, new presentations and lifecycle projects for on market programs on time and within budget
•Proactively identify and drive technical and project plan related issues to closure by working with all relevant functional lines and effectively troubleshooting and driving decisions
•Manage multiple projects concurrently, operating with minimal supervision
•Understand project drivers, requirements, scenarios and options. Proactively drive development of contingency and/or risk mitigation plans.
•Manage competing timelines and make difficult decisions regarding priorities among projects.
•Effectively communicate and present project status to Operations senior management and stakeholders
•Accountable for setting program and project plans, including timelines and expenses, that meet business and organizational objectives and ensuring those plans are achieved.
•Define budget requirements and report monthly actuals, LBE, and Plan/LRP schedules per financial schedule
•Bachelor’s Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence
•10+ years of combined experience in positions related to process development, project management, engineering/process support and manufacturing
•Must have strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations
Qualification
Bachelor’s Degree in EngineeringStrong knowledge of GMP Manufacturing
Required
Bachelor’s Degree in Engineering, science, or closely related discipline, or equivalent technical experience
10+ years of combined experience in process development, project management, engineering/process support and manufacturing
Strong knowledge of GMP Manufacturing, Supply Chain, Validation, Engineering, CMC technical development and pharmaceutical regulations
