Associate Director, Transformation Program Management

Associate Director, Transformation Program ManagementAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio.Purpose: The Associate Director, Transformation Program Management, leads and is accountable for successful delivery of large-scale transformation programs and strategic initiatives across the organization. This role builds strategies and implementation plans to drive business transformation, operational excellence, and continuous improvement to support departmental and enterprise-wide objectives. The Associate Director will serve as a key contributor in program planning, stakeholder engagement, and outcome delivery, ensuring that projects meet their objectives related to efficiency, agility, and business value.Main Responsibilities:Lead and manage complex cross-functional project and program teams, overseeing creation and maintenance of key artifacts such as program charters, status reports, work plans, and stakeholder engagement models.Ensure program compliance with relevant corporate, quality, and operational policies and procedures.Build and maintain trusted relationships at all organizational levels, providing leadership to advance transformation priorities.Identify and recommend opportunities for transformational improvement using recognized methodologies (e.g., Lean Six Sigma, Kaizen).Advise and strategize with executive sponsors and business leads on program direction, key decisions, and change management.Manage full program lifecycle: set team accountabilities, resolve issues and risks, and deliver regular executive updates/recommendations.Partner with business and functional leaders to implement new initiatives that drive productivity, compliance, efficiency, and business strategy.Ensure projects and programs are delivered on time, within scope, and with strong business impact.Oversee resources planning to meet critical program and day-to-day staffing needs, with dotted-line reporting to senior leadership.Qualifications:Minimum Bachelor's Degree required preferably in Physical or Life Sciences, Pharmacy, or Engineering; Master's Degree or PhD preferred.Certified Quality Engineer or formal training in quality engineering or statistics is preferred15+ years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical, biologics, device or chemical industryMust have a basic understanding and working knowledge of the physical and chemical characteristics of the products, including raw materials, manufactured at the plant.Must be familiar with use of statistical quality systems, electronic document management and laboratory information management.Must also be familiar with Quality policies as well as cGMP and other regulatory requirements.Must have effective people management and communication skills necessary to supervise those reporting directly or through subordinates as well as establish and maintain effective working relationships among other key individuals in manufacturing, materials management, engineering, product development, Quality Systems, Product QA, Quality Control, Information Systems and Regulatory Affairs and must demonstrate sound judgment in evaluating and acting on day-to-day situations.Strong communication Skills, both oral and written10+ years of supervisory/technical leadership experienceAdditional Information:The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.This job is eligible to participate in our short-term incentive programs.AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: Fraud AlertAbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process.If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks.If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately.Protect yourself by verifying job offers and communications. Your safety is important to us.Pay Range: $141500 - 268500 USDWhere We Work:Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.