Supervisor, Audit

AbbVie

Quick summary

Work type: On-site
Location: North Chicago, IL
Posted: 11 days ago
Closes: Jun 16, 2126
Nearby: 99+ roles within 25 mi

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Salary context

How this pay compares to similar roles

Similar $178k

$133k most similar roles pay here $227k

This listing doesn't post a salary. Most similar roles pay $143,678–$212,500.

Based on 240 similar postings.

Employer

About AbbVie

AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines and solutions in immunology, oncology, neuroscience, and eye care. Its products include Humira, Skyrizi, and Rinvoq.

AbbVie currently has 36 open roles on FindRole.

Listed pay typically runs $109,500–$208,500 across 5 roles with salary data.

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At a glance

TL;DR · Supervisor, Audit

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Join AbbVie’s Corporate Audit team as a Senior Auditor/Lead, contributing to the strategic assessment and improvement of quality systems across various therapeutic areas including immunology, oncology, neuroscience, and eye care. Your primary responsibilities will include conducting comprehensive audits for compliance with US and foreign regulations, providing constructive feedback on quality-related systems, and ensuring corrective actions are effectively implemented. You will collaborate closely with R&D QA to coordinate joint audits and communicate audit activities with internal stakeholders such as procurement and manufacturing sites, while also engaging external suppliers. This role requires a Bachelor’s degree in a technical or scientific field, at least 6 years of relevant experience including 4+ years in Quality Assurance, and knowledge of GMP regulations. Strong communication skills and the ability to influence both internal and external stakeholders are essential.

Skills

GMP ISO FDA EU-GMP ICH ASQ SAP Microsoft Excel Project Management Pharmaceuticals Medical Devices Biotechnology Quality Assurance Risk Management Regulatory Affairs Change Control CAPA Lean Six Sigma Root Cause Analysis

What you'll do

Assesses compliance of systems, facilities, and procedures per applicable regulations.
Provides feedback on audit observations and reviews corrective actions for effectiveness.
Participates in strategic initiatives to improve regulatory compliance.
Coordinates joint audits with R&D QA.
Ensures supplier audit activities align with internal stakeholders' needs.
Maintains adherence to the annual audit schedule without delaying product launches.

What we're looking for

Bachelor’s Degree in technical or scientific field (Chemistry, Pharmacy, Biology, Microbiology, Engineering) or equivalent industry experience.
6+ years of total relevant experience, including 4+ years in Quality Assurance and 2+ years in compliance/auditing.
Technical background with knowledge of GMP regulations for quality systems and compliance.
Experience in pharmaceutical, medical device, biotechnology, cosmetics, eye care, or aesthetics industries.
Excellent oral/written communication skills and strong interpersonal abilities.

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