Device Quality Senior Manager
North Chicago, ILJob$125K/yrSeen 2 days agoSeen in employer's feed 2 days ago
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Job overview
The Device Quality Senior Manager supports quality system integration for medical devices and combination products, helping ensure business objectives and global regulatory compliance. The role develops and sustains quality assurance policies and procedures, oversees cross-functional device management and quality system implementation, and supports product introductions and design changes. It also manages training, represents AbbVie in industry groups, and works with department leadership on strategic initiatives.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
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, (https://www.linkedin.com/company/abbvie/) Facebook, Instagram (https://www.instagram.com/abbvie/) , X (https://twitter.com/abbvie) and YouTube. (https://www.youtube.com/user/AbbVie)
Job Description
Responsible for supporting quality system integration activities for the Medical Device and Combination product business. This role will support the strategic direction to ensure business objectives are met to support and sustain the Combination Products and medical devices. Complete quality assurance activities to develop, implement, and sustain required device regulations to comply with global medical device and Combination Product Regulations and assure proper integration and support of device regulations.
- Areas of direct responsibility include development of Quality Assurance policies and procedures for medical devices and Combination Product regulations that support the AbbVie business objectives, functional area strategies, and the Medical Device Center.
•Manage and oversee the interrelated function activities related to medical device management including design control with Research and Development, Manufacturing Science and Technology, Supply Chain, Program Management, Commercial, Medical, Pharmacoviligance, and Regulatory Affairs. Coordinate quality system elements, training, continuous improvement, and tactical support across functions, plants, and affiliates.
•Responsible for implementing the quality system for medical devices and combination productions including compliance with Corporate, Division, and Site policies.
•Support new product introduction for pharmaceutical products, medical devices, or combination products. Support design changes to existing medical devices and combination products.
•Oversee the management of training for revised quality system polices and procedures for the medical device and combination products quality operation.
•Represent AbbVie on external industry groups where appropriate.
•In association with the Medical Device Centre, Regulatory Affairs, R&D & Operations Quality Management, manage the consolidation of the quality oversight of medical device and combination products.
•Works with the director and with the department to achieve related goals and strategic initiatives.
Qualifications
•Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering, or other technical or scientific area.
•At least 8 years’ experience with quality assurance and/or quality system oversight. Device regulation experience preferred.
•Leadership of other technical professionals and experience in leading cross-functional teams with results orientation. Skilled in the strategy development, initiation, selection, coordination, and management of projects and have the ability to solve unique problems.
•Knowledge of regulations and standards affecting devices, biologics, and pharma products. Knowledge of International Organization for Standardization (ISO) standards, US Code of Federal Regulations, and the EU regulations. Previous experience with regulatory agency interface preferred.
•Understands impact of specific area system changes to other quality systems as well as changes within division requirements and impact to specific area of control and able to adjust accordingly.
•Conflict resolution skills including persuasive management techniques required. Strong oral and written communication skills needed. Excellent interpersonal skills a plus.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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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.
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
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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
Salary: $124,500
How this job compares
Set against the 4,804 open Quality Assurance jobs on Olive Jobs, counted November 12, 2026.
- Pay
- This posting$125K/yr
- Illinois median$87–132K/yr90 salary ranges
- US median$88–143K/yr2,154 salary ranges
This rate, $125K, is 6% above the Illinois median midpoint ($117K) — in the middle half of Quality Assurance salary ranges in Illinois.
- Openings
- Olive Jobs lists 147 open Quality Assurance jobs in Illinois and 4,804 across the US. 3% of them nationwide are listed as remote or flexible.
- Hiring the most in Illinois
- AbbVie (this employer)8 open
- CDM Smith8 open
- PCI Pharma Services7 open
- Experience
- This posting asks for at least 8 years of experience — more than three in four Quality Assurance postings that state a minimum ask for (median 5 years, across 3,703 postings).
- Education
- This posting asks for a bachelor's degree; 1,659 of the 4,804 open Quality Assurance jobs (35%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 12, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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