Job opportunity
Senior Clinical Quality Assurance Manager
AbbVie Inc.
Lead clinical quality assurance for AbbVie’s global Affiliate research, applying quality systems and regulatory expertise to support clinical development. Travel across AREA may reach 35% as needed.
As Senior Manager, you will provide proactive quality management across designated countries and regions within AbbVie’s RDQA AREA organization. The work supports clinical research, quality excellence, regulatory preparedness, and first pass approvals. You will oversee compliance, risk management, audits, inspections, and quality strategy while collaborating with clinical development leaders, Affiliates, and RDQA functions.
Key Responsibilities:
Drive proactive quality management across designated countries and regions
Develop risk identification, mitigation, and control strategies
Oversee quality governance, compliance, and regulatory preparedness
Support health authority inspections, audits, and supplier qualifications
Mentor AREA managers, associates, and line management
Requirements:
Bachelor’s degree in medical science or equivalent technical experience
Eight-plus years in biopharmaceutical, medical device, or related functions
Three years leading people, initiatives, or projects
Thorough knowledge of quality systems and auditing standards
Strong regulatory, analytical, communication, and influencing skills
Bring clinical research quality, audit leadership, and regulatory expertise to AbbVie’s Affiliate operations across the AREA region.
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Apply on source site As Senior Manager, you will provide proactive quality management across designated countries and regions within AbbVie’s RDQA AREA organization. The work supports clinical research, quality excellence, regulatory preparedness, and first pass approvals. You will oversee compliance, risk management, audits, inspections, and quality strategy while collaborating with clinical development leaders, Affiliates, and RDQA functions.
Key Responsibilities:
Drive proactive quality management across designated countries and regions
Develop risk identification, mitigation, and control strategies
Oversee quality governance, compliance, and regulatory preparedness
Support health authority inspections, audits, and supplier qualifications
Mentor AREA managers, associates, and line management
Requirements:
Bachelor’s degree in medical science or equivalent technical experience
Eight-plus years in biopharmaceutical, medical device, or related functions
Three years leading people, initiatives, or projects
Thorough knowledge of quality systems and auditing standards
Strong regulatory, analytical, communication, and influencing skills
Bring clinical research quality, audit leadership, and regulatory expertise to AbbVie’s Affiliate operations across the AREA region.
#J-18808-Ljbffr