Global Product Quality Leader

Allergan; Chicago, Northern (IL, KY); Hybrid; USD 120,000 - 190,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie is seeking a seasoned Quality Assurance leader to oversee product transfer activities and maintain alignment with third party manufacturers, R&D, and regulatory affairs. You will drive quality strategy across pharmaceuticals, biologics, devices, and combinations, ensuring compliant submissions and optimal product launches.

Responsibilities include guiding cross-functional teams, escalating risk, and implementing robust quality systems.

Qualifications

• Bachelor’s Degree in Life Science or related field is required.
• Graduate degree is desirable for advanced roles.
• Strong knowledge of regulatory requirements and quality systems in pharma.

Responsibilities

• Lead a team of Quality professionals for product transfer activities and direct cross-functional team members to achieve on-time quality deliverables.
• Develops Global Product Quality Assurance strategy to support pharmaceuticals, biologics, devices and combinations.
• Primary QA contact between third party manufacturers, R&D and AbbVie Operations for submissions and regulatory interactions.
• Make key decisions on product quality, compliance and regulatory conformance for various product types.
• Manage relationships with external manufacturers and internal stakeholders to align quality expectations and timelines.
• Lead audits planning and readiness activities with QA and regulatory teams.

Skills

Quality management

Regulatory knowledge

Leadership

Project management

Problem solving

Communication

Education

Bachelor's degree in Life Science or technical field

Graduate degree preferred

Job description

AbbVie is seeking a seasoned Quality Assurance leader to oversee product transfer activities and maintain alignment with third party manufacturers, R&D, and regulatory affairs. You will drive quality strategy across pharmaceuticals, biologics, devices, and combinations, ensuring compliant submissions and optimal product launches.

Responsibilities include guiding cross-functional teams, escalating risk, and implementing robust quality systems.