OverviewSenior Manager, Third Party Manufacturing (TPM) will be the main supplier relationship contact responsible for providing the organization, supervision, strategic initiatives, and technical support necessary to manage supply of designated products. The role ensures high quality product manufacturing in compliance with local and international regulations, and release and delivery according to forecasts, schedules, and cost plans. This position also manages projects and programs that maximize profitability and ensure a cost effective, marketable, and manufacturable product throughout its life cycle. Through matrix management of cross functional groups, the Senior Manager, TPM leads teams without direct authority and coordinates operations for existing and new products manufactured with the supplier.Company DescriptionAbbVie\'s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. AbbVie aims to have a remarkable impact on people\'s lives across therapeutic areas including immunology, oncology, neuroscience, and eye care, and in Allergan Aesthetics products and services. For more information, please visit www.abbvie.com.ResponsibilitiesParticipate in the negotiation of the Manufacturing Service Agreement and amendments, and ensure compliance with the terms of the agreements.Ensure effective planning and material procurement strategies are in place to supply the TPM with the required materials.Communicate product forecasts to the TPM and agree on manufacturing and delivery schedules; coordinate with Supply Chain and Planning to meet demand forecasts.Participate in development of Financial Operating Plan, Updates, LRP, and Standard processes; ensure financial goals are met.Coordinate the Steering Committee and monitor Virtual Operation Teams to evaluate performance, address issues, and escalate when necessary.Review status reports and prepare updates for senior leadership.Collaborate with technical and quality teams to review process performance, quality trends, and implement process improvement plans.Establish governance, guidelines, and communication channels; ensure supplier quality systems and documentation meet regulatory requirements and manage inspections and commitments.Coordinate with QA on annual quality management reviews and periodic audits; ensure deviations are investigated and product dispositions are timely; establish and track performance metrics.Develop, implement, and manage programs/projects with scope, cost, time, resource management, communication, and risk management through initiating, planning, and executing phases.QualificationsBachelor\'s Degree, preferably in science or technical field.MSc or MBA preferred.Minimum 10+ years in manufacturing, engineering, project management, quality, or related areas.Broad business perspective and understanding of manufacturing processes; strong project management and influencing abilities.Experience managing subcontracted relationships preferred.Proven leadership with strong communication skills (listening, verbal, presentation, and written).Strong strategy development and planning skills with knowledge of pharmaceutical development, manufacturing and supply activities.Strong problem identification and solution development abilities; team player with ability to work in a global environment.Knowledge of business financial systems and tools.Additional InformationAbbVie is an equal opportunity employer and is committed to integrity, innovation, and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only — to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html. Reasonable accommodations information available at https://www.abbvie.com/join-us/reasonable-accommodations.html
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