Demo

Associate Director, Program Management - Hybrid

BioSpace
North Chicago, IL Full Time
POSTED ON 11/2/2025
AVAILABLE BEFORE 12/1/2025
Company Description

AbbVie'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 immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

The ME&C Associate Director is a global program management expert responsible for managing major global programs and projects across disciplines and multiple manufacturing locations. They organize and lead high-performing cross-functional teams in the planning and execution of Biologics and/or Toxin industrialization programs with experience in drug substance and/or drug product transfers.

The program manager is to provide strategic oversight for one or more industrialization programs, responsible for ensuring that each program achieves its business objectives supporting both AbbVies pipeline products and lifecycle. This individual provides leadership and coordinates program management for all manufacturing and/or technical activities needed to ensure successful transfer and industrialization of the assigned products.

The chosen candidate is to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable program execution strategies with clearly defined deliverables and milestones. The program manager is to kick-off project/transfer teams, remove barriers to success, realize opportunities, mitigate risks and successfully drive completion of program deliverables.

Success in this role requires a passionate, pro-active program manager with exceptional organizational skills, an enterprise leadership mind-set and the ability to engage, align and empower functional and project managers in Manufacturing, Engineering, Product Development Science & Technology, Quality, Supply Chain, Trade Compliance and Procurement.

Responsibilities

  • Using a collection of program management tools, independently define and document the program scope, execution strategies, resources, deliverables and milestones. Create, implement and maintain PM tools.
  • Develop cost estimates, secure funding/resources through Financial Planning and Long-Range Planning processes, manage the program per plan, report actual and forecasted spend and resolve financial variances.
  • Assemble and lead cross-functional resources in a manner that results in the formation of effective, inclusive, high-performing teams with success-oriented focus. Mentor and develop program and project managers.
  • Articulate the program execution strategy, deliverables and milestones to appropriate internal and external stakeholders maintaining a clear, consistent narrative to foster engagement, understanding and alignment.
  • Work collaboratively with the program team to implement effective program governance structures, work breakdown structures, roles and responsibilities, integrated timelines and communication plans.
  • Develop risk mitigation and contingency plans; implement as needed to keep the program on track.
  • Identify and realize opportunities that result in acceleration, efficiency and cost avoidance/reduction. Understand and integrate changes in the global landscape for device and combination product industrialization, global quality and regulatory requirements and pathways for approval/market access in programs to deliver acceleration and value.
  • Ensure the program team and stakeholders are aligned and the program is being executed efficiently. Manage competing timelines and make difficult decisions regarding priorities across the program. Drive rapid identification, communication and resolution of issues. Enable informed decision making, robust cross-functional problem solving and continuous improvement of program management practices and tools.
  • Plan and facilitate program meetings, document minutes and actions, follow-up on closure, and hold team members accountable for decisions and deliverables.
  • Ensure that programs and projects are technically and financially closed out upon completion and any on-going responsibilities are formally transferred to appropriate parties.


Qualifications

  • Bachelors Degree in Engineering, science, or closely related discipline, or equivalent technical experience plus demonstrated competence, MBA preferred
  • 15 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
  • Must have demonstrated organizational and planning skills, excellent verbal and written communication skills while managing large programs in the pharmaceutical industry
  • Must have demonstrated strong project management skills with successful delivery of projects. Demonstrated ability to operate effectively with minimal to no supervision.
  • Must be able to effectively facilitate the resolution of complex scientific, technical, analytical and business issues across functional lines
  • Significant plant experience a must
  • Demonstrated ability to effectively communicate with senior and executive management.
  • PMP certification a plus
  • Proficiency in multiple languages a plus


Note: Compensation and grading for roles may vary depending on location.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

  • The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
  • This job is eligible to participate in our short-term incentiveprograms.
  • This job is eligible to participate in our long-term incentiveprograms


Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employee remains in the Company's sole andabsolutediscretion unless and until paid andmay be modified at the Companys sole and absolute discretion, consistent withapplicable law.

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, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Salary.com Estimation for Associate Director, Program Management - Hybrid in North Chicago, IL
$137,376 to $170,025
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