Senior QA Specialist, Clinical Supplies & Compliance

AbbVie Inc.; North Chicago (IL); On-site; USD 85,000 - 125,000; Full time

Benefits offered by this job

401(k)

Medical/dental/vision insurance

Paid time off

Job summary

AbbVie Inc. in North Chicago, IL seeks a Quality Assurance professional to support batch disposition and ensure high-quality clinical supplies are compliant with global regulatory standards.

You will collaborate across functions to review records, support audits, and drive continuous quality improvements in a fast-paced manufacturing environment. The role emphasizes strong analytical and communication skills, cross-functional teamwork, and the ability to resolve complex quality issues while

Qualifications

• 4+ years in QA, production, or testing of pharmaceutical APIs or drug products.
• Experience with GMP facilities and regulatory compliance.
• Strong problem-solving and communication skills.

Responsibilities

• Review and approve batch records and release materials per procedures.
• Support audits by regulators, customers, and R&D GxP Compliance.
• Provide QA approvals in MRP system and manage CAPAs and deviations.
• Review clinical documentation and specifications.
• Lead project teams to anticipate and resolve quality issues.
• Monitor process effectiveness and drive quality improvements.

Skills

Quality Assurance

Documentation

Analytical skills

Communication

Cross-functional collaboration

Education

Bachelor’s degree in life sciences or related field

Job description

AbbVie Inc. in North Chicago, IL seeks a Quality Assurance professional to support batch disposition and ensure high-quality clinical supplies are compliant with global regulatory standards.

You will collaborate across functions to review records, support audits, and drive continuous quality improvements in a fast-paced manufacturing environment. The role emphasizes strong analytical and communication skills, cross-functional teamwork, and the ability to resolve complex quality issues while