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New · posted Oct 22

AbbVie · Pharmaceuticals

Manager Regulatory Affairs, Global Regulatory Strategy US & Canada

  • North Chicago, IL
  • Hybrid
  • Full-time
  • Manager
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EmploymentFull-time
Deadline

Open until filled

The role

The Manager Regulatory Affairs, Global Regulatory Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development.
This individual assists Regulatory Staff by identifying and gathering data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured or distributed to meet relevant US and Canada regulatory requirements.

What you need

What you'll do

  1. Responsible for a product(s) within a Therapeutic Area and supports the Manager (Senior Manager, Associate Director, Director (Global Regulatory Lead (GRL), in the development & execution of the regulatory strategy.
    Assigned matters may have an impact on business activities and operations.
  2. Serves as Health Authority (HA) liaison with FDA for routine communications in support of filings including complete and timely responses during application review.
    Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial.
    Functions independently in negotiation and decision-making for project related issues that have cross-functional impact.
  3. Key contributor responsible for the preparation and review of regulatory submissions consistent within US and Canada regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review.
  4. Supports the regulatory submission and approval process.
    Applies regulatory/technical knowledge of government regulations and skills across therapeutic areas.
  5. Recommends and implements changes to projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidances, as well as corporate policies and management-related considerations.
  6. Presents pertinent regulatory information to appropriate cross-functional areas.
  7. Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP).
  8. This role will work a hybrid work schedule (3 days in office) from AbbVie Lake County, IL headquarters.

Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required

  1. Required Education: Bachelor’s degree (pharmacy, biology, chemistry, pharmacology) or industry related.
  2. Preferred Education: Advanced Degree a plus. Certifications a plus.
  3. Required Experience: 6 years Regulatory, R&D, or Industry-related experience.
  4. Preferred Experience: 2-3 years in pharmaceutical regulatory activities
  5. Skill Set:
    • Proven skill at implementing successful US and Canada regulatory strategies, global regulatory experience is a plus.
    • Experience working in a complex and matrix environment.
  6. Skill Set cont'd:
    • Good communication, both oral and written.
    • Experience interfacing with government regulatory agencies.
    • Demonstrates good negotiation skills and builds consensus.

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

  1. 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. ​
  2. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​
  3. 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, ILHybridOpen in Maps (opens in a new tab)

More jobs in North Chicago, IL
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 · 51 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 23, 2026

Salary intelligence

How the pay compares

This role's midpoint is 1% below the US median for Regulatory Affairs roles at this level.

This roleEmployer provided

$110,000 to $209,000 a year

Manager roles in Illinois5 roles publishing pay

Middle half $150,500 to $180,500, median $159,500

Manager roles in the US54 roles publishing pay

Middle half $147,875 to $174,625, median $161,250
Annual base pay
Annual base payLowMedianHigh
This role$110,000—$209,000
Illinois$150,500$159,500$180,500
All US$147,875$161,250$174,625

This role: AbbVie's own published range. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, October 23, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Regulatory Affairs

The general path across 315 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not AbbVie's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Regulatory Affairs Specialist · Summer 2027 Internship

    $92K median39 open
  2. One step back

    Senior & Principal

    Often: Senior Regulatory Affairs Specialist · Principal Regulatory Affairs Specialist

    $138K median75 open
  3. This role

    Manager

    Often: Regulatory Affairs Manager · Manager, Regulatory Affairs

    $161K median68 open
  4. Next step

    Director

    Often: Senior Director, Regulatory Affairs · Director, Regulatory Affairs

    $236K median116 open
  5. Later

    VP & Executive

    Often: Global Head of Injectable Aesthetics Regulatory Strategy · Global Head of Regulatory Affairs, Roche Diagnostics

    $323K median17 open

Skills DNA

What this role leans on

How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 3 linesDocumentation and SOPs: 1 lineRegulatory submissions: 6 linesCollaboration and leadership: 4 linesGMPDocumentationSubmissionsTeamwork
  • Regulatory submissions6
  • Collaboration and leadership4
  • GMP and compliance3
  • Documentation and SOPs1

Company hiring pulse

AbbVie on Regulatory Jobs

51
Open roles
31
Distinct roles
11
Locations

By discipline

  • Regulatory28 55%
  • Quality22 43%
  • Compliance & Safety1 2%

By level

  • Director22 43%
  • Manager15 29%
  • Senior & Principal9 18%
See all 51 AbbVie roles

More roles at AbbVie

All 51 AbbVie roles

Similar Regulatory Affairs roles elsewhere

Manager Regulatory Affairs, Global Regulatory Strategy US & Canada at AbbVie

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

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