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Director, QA R&D - PV Audits

AbbVie
Full-time
Remote friendly (North Chicago, IL)
United States
$156,000 - $296,500 USD yearly
Operations

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Role Summary

Director, QA R&D - PV Audits. Responsible for implementing a comprehensive audit program and leading a high-performing team of audit staff to assure the PV system has proper quality, integrity and controls via strategic audit oversight. Ensure R&D compliance with corporate policies and worldwide regulations, and provide consultation to R&D leadership on audit management, risk decisions, and quality improvements.

Responsibilities

  • Lead collaboration across R&D Quality, Safety and core PV System stakeholders to characterize the Audit landscape and routinely assess risks to the PV System for compliance and quality
  • Lead cross-discipline projects and strategies that benefit the PV System quality foundation and enable growth of the audit team using data and advanced technology
  • Monitor new regulations and industry trends; ensure compliance with regulations and policies within AbbVie and with external collaborations as applicable
  • Identify and manage operational and strategic issues within the audit program with governance and escalation strategies as appropriate
  • Lead the curation and maintenance of inspection-ready documentation (SOPs and evidence of execution) for Health Authority interactions
  • Oversee timely provision of data to ensure Product Safety Master File contains accurate audit-related data
  • Lead routine interactions with stakeholder leadership to ensure understanding of audit targets, improvements, and performance of the audit team and auditees
  • Lead Risk Management practices tailored to the audit program, connecting to R&D Quality, Compliance and External Partnership leaders to drive improvements and forward-looking strategies
  • Build a strategic, high-performing team executing audits and improving auditee success during external audits and inspections
  • Identify and improve connections and utilization of Quality System Elements including Risk Management, Change Management and Exception Management
  • Engage stakeholders in ongoing reviews of audit activities and achievements, fostering QA inclusion for process improvements
  • Recruit, develop, manage, and mentor a team of Quality Professionals; set goals, provide performance reviews, and manage staffing actions

Qualifications

  • Bachelor degree in a physical science, life science, nursing, pharmacy or equivalent experience
  • 10+ years of pharmaceutical industry experience
  • Pharmacovigilance experience
  • 3+ years of people leader experience (highly preferred)
  • Strong people leadership and team management skills; ability to mentor, coach, and develop high-performing audit professionals
  • Ability to balance adaptability with timely decision making to deliver core audit programs while leveraging people, processes, and technology
  • Ability to lead, prioritize, and resource plan for multiple, complex quality improvement projects
  • Change-ready mindset; ability to foster process improvement, accountability, and trust as a strategic advantage for R&D Quality

Skills

  • Quality management
  • Audit program management
  • Strategic and dynamic team leadership
  • Critical communication skills
  • Functional expertise in PV and QA
  • Analytical aptitude for subject matter

Education

  • As required by qualifications above (Bachelor degree in a physical science, life science, nursing, pharmacy or equivalent)

Additional Requirements

  • The role may be remote within the US or UK; compensation adjusted to host country
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