Future Opportunities - Join Our Talent Pipeline for Supervisor, Audit
AbbVie
August 19, 2026
Remote friendly (North Chicago, IL)
United States
$35,000 - $172,500 USD yearly
Corporate Functions
Purpose:
The Audit and Compliance Senior Auditor/Lead performs comprehensive audits for compliance with US and foreign regulation requirements, providing constructive evaluation of quality-related systems for AbbVie plants, affiliates, quality service areas, and/or suppliers providing materials, services, and products to AbbVie. Executes GMP compliance and quality activities in accordance with AbbVie policies/procedures and applicable quality/regulatory requirements to assure quality, effectiveness, and safety of products.
Responsibilities:
- Assess compliance of systems, facilities, and procedures per applicable regulations, ensuring compliance to regulatory requirements and AbbVie specifications.
- Provide audit observations and review corrective actions to verify commitments are properly implemented, effective, and maintained at suppliers or internal AbbVie sites (formulate recommendations for internal sites).
- Participate in strategic initiatives to improve compliance to regulatory requirements and standards.
- Collaborate with R&D QA to coordinate and conduct joint audits.
- Coordinate supplier audit activities with internal stakeholders (procurement, SQA, EQA, manufacturing sites, commercial affiliates) and external stakeholders.
- Ensure audits follow the annual audit schedule.
- Ensure no product launch delays or business interruptions due to supplier audit delays to assure supply to AbbVie patients.
Qualifications:
- Bachelor’s degree (technical/scientific preferred) or equivalent experience (at least 4 years); exposure to pharma/medical devices/biologics/combination products/cosmetics/eye care/aesthetics; ASQ certification desired.
- 6+ years relevant experience; 4+ years Quality Assurance (with some project management); 2+ years compliance/auditing.
- Technical background in Quality Assurance audit process and worldwide GMP quality system requirements.
- Strong understanding of quality/operational systems and quality management principles.
- Excellent oral/written communication; strong interpersonal and organizational skills; sound judgment; ability to influence internal/external stakeholders.
Benefits (as stated): paid time off; medical/dental/vision insurance; 401(k) to eligible employees; eligible for short-term incentive programs.
Application instruction:
Submit your application to this talent pipeline requisition to be added to the talent pipeline and considered for future opportunities.
The Audit and Compliance Senior Auditor/Lead performs comprehensive audits for compliance with US and foreign regulation requirements, providing constructive evaluation of quality-related systems for AbbVie plants, affiliates, quality service areas, and/or suppliers providing materials, services, and products to AbbVie. Executes GMP compliance and quality activities in accordance with AbbVie policies/procedures and applicable quality/regulatory requirements to assure quality, effectiveness, and safety of products.
Responsibilities:
- Assess compliance of systems, facilities, and procedures per applicable regulations, ensuring compliance to regulatory requirements and AbbVie specifications.
- Provide audit observations and review corrective actions to verify commitments are properly implemented, effective, and maintained at suppliers or internal AbbVie sites (formulate recommendations for internal sites).
- Participate in strategic initiatives to improve compliance to regulatory requirements and standards.
- Collaborate with R&D QA to coordinate and conduct joint audits.
- Coordinate supplier audit activities with internal stakeholders (procurement, SQA, EQA, manufacturing sites, commercial affiliates) and external stakeholders.
- Ensure audits follow the annual audit schedule.
- Ensure no product launch delays or business interruptions due to supplier audit delays to assure supply to AbbVie patients.
Qualifications:
- Bachelor’s degree (technical/scientific preferred) or equivalent experience (at least 4 years); exposure to pharma/medical devices/biologics/combination products/cosmetics/eye care/aesthetics; ASQ certification desired.
- 6+ years relevant experience; 4+ years Quality Assurance (with some project management); 2+ years compliance/auditing.
- Technical background in Quality Assurance audit process and worldwide GMP quality system requirements.
- Strong understanding of quality/operational systems and quality management principles.
- Excellent oral/written communication; strong interpersonal and organizational skills; sound judgment; ability to influence internal/external stakeholders.
Benefits (as stated): paid time off; medical/dental/vision insurance; 401(k) to eligible employees; eligible for short-term incentive programs.
Application instruction:
Submit your application to this talent pipeline requisition to be added to the talent pipeline and considered for future opportunities.