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New · posted Oct 23

AbbVie · Pharmaceuticals

Quality Systems Manager

  • North Chicago, IL
  • On-site
  • Full-time
  • Manager
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EmploymentFull-time
DeadlineOpen until filled

The role

The Manager Quality Systems is responsible for providing quality assurance support for some or all of the following manufacturing processes: pharmaceutical products, medical devices, cosmetics, combination products and biologics. This role will support the strategic direction to ensure business objectives are met. Specific areas of responsibility may include supplier qualification and approval, supplier risk management, , supplier change management, , and Approved Supplier List (ASL) governance. This position will also translate strategy into tactical objectives to deliver strategic plans and regulatory updates. This position will ensure that all product, process or system related quality activities from raw material inspection through shipment of final product are in compliance with Corporate and governmental regulations.

What you need

What you'll do

  • Ensure proper integration and support of quality regulations: drug, biologics, cosmetic, device and/or combination products.
  • Lead project teams in planning, preparation, review and approval of quality documentation.
  • Responsible for implementing and maintaining the effectiveness of the quality system for drug, biologics, cosmetic, device and/or combination products including compliance with Corporate policies, processes and procedures.
  • Design effective quality systems, procedures and/or processes within cross functional teams to ensure compliance as well as efficiency throughout our quality system. May be required to prepare and present data during regulatory audits (FDA, EMA, Anvisa, etc) and internal audits.
  • Manage and oversee the interrelated function activities including design control with R&D, Manufacturing Science and Technology (MS&T), Supply Chain, Program Management, Commercial, Medical, Pharmacovigilance, and Regulatory Affairs.
  • Coordinate quality system elements, training, continuous improvement, and tactical support across functions, plants, and affiliates.
  • Support new product introduction for pharmaceutical products, medical devices, or combination products. Support design changes to existing medical devices and combination products.
  • Interact with internal and external partners for development of best practices in our quality systems and procedures.
  • Perform assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within our quality system.
  • Oversee the implementation and management of training and education programs for various aspects of quality assurance.
  • Bachelor’s Degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/ scientific area preferred.
  • 8+ years’ experience in quality assurance, quality oversight or relevant experience.
  • Leadership of technical professionals and in leading cross-functional teams.
  • Technical knowledge in as many of the following areas as possible: Quality, Regulatory, Process Sciences, Manufacturing Operations.
  • Knowledge and familiarity with product, process, equipment, and facilities of pharmaceutical, biological or device related products.
  • Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting device, biologics, and pharmaceutical products.
  • Experience working in both team setting and independently. Works well with manager guidance while able to manage own time.
  • Strong oral (with all levels of management) and written communication skills needed.
  • Excellent interpersonal skills a plus.
  • Can lead medium to larger sized projects with increasing level of complexity and size to deliver tactical results that support strategic initiatives.

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.​

Pay and benefits

$110,000 – $209,000 a year

Employer provided
How this compares
  • Paid time off

  • Medical insurance

  • Dental insurance

  • Vision insurance

  • 401(k)

  • Long-term incentive programs

Where you'll work

North Chicago, ILOn-siteOpen in Maps (opens in a new tab)

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About forty smiling members of AbbVie's Women Leaders of AbbVie employee group posed together on a stage

From the posting

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.

AbbVie company page · 53 open roles
Equal opportunity, accessibility and legal noticesAbbVie's statements, word for word

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 applicants seeking a reasonable accommodation, click here to learn more:

Job intelligence

The context around this role

Live data · October 24, 2026

Salary intelligence

How the pay compares

This role's midpoint is 4% above the US median for Quality Assurance roles at this level.

This roleEmployer provided

$110,000 to $209,000 a year

Manager roles in Illinois8 roles publishing pay

Middle half $159,500 to $181,000, median $181,000

Manager roles in the US112 roles publishing pay

Middle half $130,875 to $167,625, median $154,000
Annual base pay
Annual base payLowMedianHigh
This role$110,000—$209,000
Illinois$159,500$181,000$181,000
All US$130,875$154,000$167,625

This role: AbbVie's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 24, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 911 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not AbbVie's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $80K median242 open
  2. One step back

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $119K median393 open
  3. This role

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $154K median144 open
  4. Next step

    Director

    Often: Director, Quality · Director, Quality Systems

    $209K median117 open
  5. Later

    VP & Executive

    Often: AVP · DX Head of Regions Quality Management and Regulatory Affairs

    $311K median15 open

Skills DNA

What this role leans on

How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 6 linesLab testing and methods: 1 lineDocumentation and SOPs: 4 linesValidation and qualification: 1 lineQuality systems and risk: 6 linesData and digital systems: 1 lineCollaboration and leadership: 8 linesGMPLab testingDocumentationValidationQuality systemsData systemsTeamwork
  • Collaboration and leadership8
  • GMP and compliance6
  • Quality systems and risk6
  • Documentation and SOPs4
  • Lab testing and methods1
  • Validation and qualification1
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

AbbVie on Regulatory Jobs

53
Open roles
31
Distinct roles
10
Locations

By discipline

  • Regulatory30 57%
  • Quality22 42%
  • Compliance & Safety1 2%

By level

  • Director24 45%
  • Manager16 30%
  • Senior & Principal9 17%
See all 53 AbbVie roles

More roles at AbbVie

All 53 AbbVie roles

Similar Quality Assurance roles elsewhere

Quality Systems Manager at AbbVie

Open until filled. $110K–$209K a year, employer provided.

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