Director, Program Management

Posted 5 Days Ago
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North Chicago, IL, USA
Hybrid
161K-305K Annually
Expert/Leader
Healthtech • Pharmaceutical
The Role
Leads multiple complex pharmaceutical manufacturing and capital programs within Engineering. Directs cross-functional teams, establishes program strategy and timelines, manages budgets and risks, supports regulatory requirements, resolves conflicts, and communicates decisions and progress to senior stakeholders. Requires strong pharmaceutical manufacturing, supply chain, CMC, project management, strategic leadership, and technical problem-solving expertise in global, multicultural environments.
Summary Generated by Built In
Company Description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Director, Program Management will be responsible for the overall program implementation and oversight for assigned manufacturing and capital programs within the Engineering organization. The individual will be required to lead a cross-functional team to ensure program deliverables are achieved with adherence to approved budgets. The individual must have the ability to work independently, and also as an effective and engaged team leader.

Responsibilities:

  • Lead and direct multiple cross-functional teams for the implementation of complex programs, managing strategy, execution and budget.
  • Establish program strategy and timelines, defining technical and regulatory requirements to support regulatory approvals.
  • Evaluate contingency plans and risk management strategies.
  • Ensure effective communication within team and to Senior Leader stakeholders.
  • Lead team discussions to resolve issues and ensure team alignment throughout program execution.
  • Define budget requirements and report monthly actuals, LBE, and Plan/LRP schedules per financial schedule.
  • Communicate program requirements, priorities and decisions, regularly and effectively.
  • Guide cross-functional team in resolving conflicts and indecision's. Escalate when necessary.

Qualifications

  • Bachelor in Science or Engineering; MBA preferred.
  • Strong knowledge of GMP Manufacturing, Supply Chain, CMC technical development and pharmaceutical regulations is required.
  • Demonstrated strong planning and project management skills while managing large, complex programs in the pharmaceutical industry.
  • PMP certification a plus.
  • 10+ years of industry experience, 5 or more years program management experience.
  • Strong strategic thinking and leadership skills.
  • Strong communication, organization, analytical, presentation, and people skills.
  • Demonstrated experience in a global and multi-cultural environment.
  • Proven ability to resolve conflict across cross-functional teams and technical experts.
  • Ability to understand technical aspects of complex systems and guide cross-functional and detailed technical discussions during critical problem solving exercises

Additional Information

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

  • 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 long-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable 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, visit https://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

Skills Required

  • Bachelor's degree in Science or Engineering
  • Strong knowledge of GMP manufacturing
  • Strong knowledge of supply chain
  • Strong knowledge of CMC technical development
  • Strong knowledge of pharmaceutical regulations
  • Strong planning and project management skills managing large, complex pharmaceutical industry programs
  • 10 or more years of industry experience
  • 5 or more years of program management experience
  • Strong strategic thinking and leadership skills
  • Strong communication, organization, analytical, presentation, and people skills
  • Experience in a global and multicultural environment
  • Ability to resolve conflict across cross-functional teams and technical experts
  • Ability to understand technical aspects of complex systems and guide technical discussions during critical problem-solving exercises
  • MBA
  • PMP certification

AbbVie Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about AbbVie and has not been reviewed or approved by AbbVie.

  • Retirement Support — Retirement programs are portrayed as a standout, with a dollar‑for‑dollar 401(k) match up to 6% and an additional annual company contribution based on age and service. Feedback suggests this materially boosts perceived total compensation for many U.S. employees.
  • Parental & Family Support — Paid parental and caregiver leave are emphasized, including up to 12 weeks of fully paid parental leave for all parents and 4 weeks of paid caregiver leave in the U.S. Feedback suggests these policies are a meaningful differentiator for employees balancing family needs.
  • Leave & Time Off Breadth — Time off is described as extensive, with tiered vacation that scales with tenure, 17 company holidays, and two paid volunteer days in the U.S. Feedback suggests the breadth of leave contributes notably to overall benefits satisfaction.

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The Company
HQ: North Chicago, IL
56,000 Employees
Year Founded: 2013

What We Do

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first — for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuroscience, eye care, aesthetics and other areas of unmet need.

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