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HomeCompaniesAbbvieGlobal Supply Chain QA Project Manager

Global Supply Chain QA Project Manager

Abbvie · North Chicago, IL, United States · Hybrid · Active · $96,500–$183,500 / year · SmartRecruiters

Job facts

FieldValue
CompanyAbbvie
TitleGlobal Supply Chain QA Project Manager
Normalized title-
Department / teamQuality Assurance
LocationNorth Chicago, IL, United States
Work modelHybrid / Hybrid
Employment typeFull Time
Salary$96,500–$183,500 / year
Statusactive
ATS providerSmartRecruiters
Posted / first seen2026-06-05 / 2026-06-06
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Abbvie.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in North Chicago.Open
Department jobsActive postings in Quality Assurance.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyAbbvie
Source78fbf4b3-4225-45c8-b041-228a3314c7ee
ATS providerSmartRecruiters

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. Leads global projects and/or programs which support various strategic initiatives within the Quality System. Responsibilities include all aspects of end-to-end project and/or program management within specific area of expertise. Actively collaborates with manufacturing sites, external manufacturing, regulatory, supply chain, product quality, compliance, and other global functions in order to successfully deliver objectives. Provides regular updates and recommendations to senior leadership in order to drive an effective Quality System. Responsibilities Develops project timelines, deliverables, conducts research analysis, monitors project status, and provides expertise for global projects/programs supporting strategic global Quality initiatives Actively collaborates with cross-functional team to complete project milestones per established timeline. Leads meetings with cross-functional partners. Utilizes expertise within GxP to review various types of content, such as external regulations or governing documents, and provide recommendations. May create and manage project/program tasks within quality software system. Builds and maintains collaborative partnerships with cross-functional stakeholders at all levels of the organization to understand business needs and incorporate these into assigned project/program decisions. Manages end-to-end lifecycle of project/program, including driving team accountability, addressing project risks, driving effective decision making. Creates and continuously improves meaningful metrics to demonstrate effectiveness and performance of assigned project/program. Monitors changes in external regulations and project manages changes to internal processes accordingly. Effectively delivers project or program status updates and recommendations for future strategic initiatives to senior leadership Bachelor’s degree in Science/Engineering/Business Management or equivalent technical work experience 5+ years of relevant Quality experience in a GMP pharmaceutical, biologics, and/or medical device manufacturing environment Strong understanding of cGxPs, regulatory inspections, regulatory documents, global regulations, and standards Experience in Project Management and leading cross-functional project teams with technical professionals in a global and/or complex, matrixed organization Strong oral and written communication, interpersonal, time management, influence, and problem-solving skills Proficient in the use of standard software applications including Office 365 Validation experience with equipment, facility, utilities and/or process validation 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 roleat  the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors  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. ​ Note: No amount of pay is  considered to be wages or compensation until such amount isearned,  vested,  and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that areallocable 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 absolutediscretion,  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

Full job record

Job ID9f284774ce5c5d72379ff89b2ed21ad2179488fa
Org ID85ca9fcd-dbd3-4f34-8622-ce60ce7ee353
Source ID78fbf4b3-4225-45c8-b041-228a3314c7ee
Board ID78fbf4b3-4225-45c8-b041-228a3314c7ee
Providersmartrecruiters
Provider Job Key3743990013495607
TitleGlobal Supply Chain QA Project Manager
Normalized Title
Statusactive
Activeyes
Location TextNorth Chicago, IL, United States
DepartmentQuality Assurance
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
RegionIL
CityNorth Chicago
Salary RawUSD 96500-183500 year
Salary Min96,500
Salary Max183,500
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.smartrecruiters.com/AbbVie/3743990013495607-global-supply-chain-qa-project-manager
Apply URLhttps://jobs.smartrecruiters.com/AbbVie/3743990013495607-global-supply-chain-qa-project-manager?oga=true
First Seen At2026-06-06 10:45:35Z
Last Seen At2026-06-06 10:45:35Z
Last Checked At2026-06-06 10:45:35Z
Last Changed At2026-06-06 10:45:35Z
Inactive At
Source Posted At2026-06-05 17:08:56Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=smartrecruiters/board=abbvie/date=2026-06-06/2026-06-06T10-45-26-237Z-add6ce205f3d964e8bf0951cb095a328af3cd9fe0cba97e1cc24d417318dd120.json
Event Fields
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Parsed Structured
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  "salary_period": "year",
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  "salary_currency": "USD"
}
Extensions
{}
Native Structured
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