Associate Director, Engineering

AbbVie Tempe, us Full-time Updated 24 August 2026
Pharma

Job 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 at&#xa0; www.abbvie.com . Follow @abbvie on&#xa0; X ,&#xa0; Facebook ,&#xa0; Instagram ,&#xa0; YouTube ,&#xa0; LinkedIn &#xa0;and&#xa0; Tik Tok . Provide overall direction to the Engineering organization including Process, Capital, Maintenance, Metrology, Utilities and Facilities. Directs the engineering teams and activities for new product introduction, commercial and clinical manufacturing. The role is accountable for Maintenance Excellence Program (MEP) metrics and the Perfect Index, leads the Capital Plan and LRP. In addition, the role provides leadership and direction for all&#xa0;Medical Device&#xa0;performance related activities on site, delivering&#xa0;quality and compliance&#xa0;across site. The role directs a cross functional team to drive initiatives that enable and deliver the highest standards of&#xa0;Medical Device Manufacturing&#xa0;performance. The position is on the Site Leadership Team and advises the Manufacturing Site Director and extended Operations leadership team on strategy and business priorities. Accountable for all processes, policies, procedures and execution related to Process Engineering, Capital Planning and Projects, Maintenance, Metrology, Utilities and Facilities Effectively leads the multi-disciplinary team to develop resource plans for approved projects and make recommendations regarding use of internal and/or external resources for projects/facility planning, design and execution. Responsible for maintaining&#xa0;medical device production systems&#xa0;in an audit-ready state of compliance at all times over the lifecycle from initial validation through retirement. Directs&#xa0;GMP and non-GMP&#xa0;equipment, facility and utility projects to ensure adherence to AbbVie Standards and Specifications. Establishes and maintains appropriate relationships with internal (manufacturing, quality, engineering and other areas) and external partners to coordinate and execute project plans to meet project design, schedule, cost and quality requirements. Responsible for strategic planning and facility asset utilization that advances the site, continually looks for opportunities for process optimization, cost avoidance and reduction. Leads and oversees discipline specific engineering expertise to provide&#xa0;Medical Device&#xa0;benchmarking of process equipment and&#xa0;quality system best practices&#xa0;within AbbVie. Responsible for managing and leveraging common engineering systems including SAP, Maximo, Meridian, and achieving maintenance and metrology schedules and deliverables/ Develop and manage staff through hiring, managing performance, developing talent and providing clear expectations. Coach the associate directors, managers and supervisors in the organization and establish clear expectations with all employees regarding responsibilities, goals and behaviors. Acts as site Subject Matter Expert for&#xa0;medical device manufacturing&#xa0;on site across all functions including Manufacturing, Quality,&#xa0;Regulatory, and Engineering. Drives all aspects of&#xa0;manufacturing performance&#xa0;on site through analysis of data, engagement of Site colleagues and development/execution of action plans. Drives a culture of Speak-Up. Accountable for the site&#xa0;quality and compliance strategy, owns and advises the Site Lead Team on the&#xa0;medical device quality program, championing and owning any recommendations for improvement of the&#xa0;quality management system. Drives the implementation of Best Practices related to&#xa0;Medical Device Manufacturing. Bachelor’s Degree required, in Engineering or equivalent. Masters Degree preferred. 10 - 15 years of experience in Manufacturing and Engineering discipline Business acumen coupled with functional leadership experience is required to drive high performance in a complex manufacturing operation Must have demonstrated organizational and planning skills, excellent verbal and written communication skills Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&#xa0;local law:&#xa0;​ The compensation range described below is the range of possible base pay compensation that the Company&#xa0;believes in&#xa0;good faith it will pay for this role at the time&#xa0;of this postingbased on the job grade for this position.&#xa0;Individual&#xa0;compensation paid within this range will depend on many factors including geographic location, and&#xa0;we&#xa0;may ultimately&#xa0;paymore or less than the posted range. This range may be modified in the&#xa0;future.&#xa0;​ </li

Stand out for this role

NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.

Tailor my CV now — free to try