QA Associate Director - GCP / PV Regulatory Inspections

Company: IQVIA LLC
Location: Durham
Posted on: March 18, 2023

Job Description:

QA Associate Director - GCP / PV Regulatory Inspections page is loaded QA Associate Director - GCP / PV Regulatory Inspections Apply locations Durham, North Carolina, United States of America Topeka, KS Aurora, Illinois, United States Detroit, MI Joliet, IL time type Full time posted on Posted 12 Days Ago job requisition id R1349192 Remote Opportunity Summary: The IQVIA Quality Assurance team is a dynamic, talented, and experienced global team that owns the global quality management system for the largest human data science company in the world. The QA function is responsible for driving compliance in a highly regulated industry through audits, hosting customer audit and regulatory inspections, functional support, issue & CAPA management, regulatory consultancy, management of data analytics and customer relationship interactions. These services ensure our clinical research activities are of the highest quality. We proactively support our business partners and help to drive innovation. Continuous improvement is a core capability and we value strategic thinking, creativity and operational excellence. We seek highly motivated people who truly want to make a difference in the life sciences industry and are looking for opportunities to impact the business and be part of the solution. At IQVIA, we support our colleagues with a focus on succession planning, career progression and continuous learning. Purpose:
This QA Associate Director will provide insight, which is exercisable across the large part of the organization, or by managing a team of managers by influencing outcomes. Oversee & coordinate assigned QA program in support of customer accounts, functional accounts, audit and inspection program, or QA quality management system at a regional and/or global level. Provide insights, analyses and support in the assessment and promotion of compliance with regulations, guidelines, and operating procedures, risk identification and mitigation, Quality, Process, productivity/efficiency improvement initiatives. Act as line manager for one or more QA staff and oversee development and departmental deliverables. Manage the quality assurance oversight of projects, assignments, training and staff.Responsibilities:

• The Associate QA Director role supports mainly the hosting of regulatory inspections at IQVIA, specifically PV Inspections, as well as sponsor and customer audits at the sponsor. He/she may also support customer audits at IQVIA, if required.
  • Plan, schedule, conduct, report and close audit activities, as assigned
  • Host customer audits and participate in review of corrective action plans, as assigned
  • Provide Quality Assurance support, guidance and management of Quality Issues, as assigned
  • Recommend systems for audit, write systems audit plans, coordinate scheduling, conduct, reporting and closure of internal system audits
  • Serve as the QA Contact for assigned internal/external customers and IQVIA functional areas
  • Oversee proper coordination of customer-initiated audits and mock regulatory inspections, manage regulatory facility inspections, as assigned
  • Oversee documentation, reporting, and closure of compliance issues
  • Assist in the enhancement -of Quality Assurance and control policy, and risk identification and mitigation by providing consultation & recommendations to regional and Global QA Management
  • Serve as an author for QA Standard Operating Procedures (SOPs), and act as regional QA representative to the global QA SOP taskforce
  • Provide guidance, interpretation, support, training, and key input to development groups for consultation and interpretation of regulations, guidelines, corporate standards, and policies
  • Support Quality Management in proposal reviews and reporting QA metrics
  • Conduct trend analysis of audit results, provide to internal/external stakeholders as agreed, as assigned
  • Participate in or lead (cross functional) teams for special projects as assigned
  • Promote the concept of quality, the principles of quality management and devise and implement quality improvements
  • Manage staff, including planning, assigning, & directing work, appraising performance, guiding professional development, rewarding and disciplining employees, addressing employee relations issues & resolving problems. Approve actions on human resources mattersRequired Education and Experience:
    • Bachelor's Degree preferred
    • 10 years of GCP Quality Assurance experience in Biopharmaceutical industry, with a focus in development and post-marketing (mainly PV).
    • 3 years of Management experience, within Quality Assurance
    • Experience Hosting Regulatory Inspections, specifically PV Inspections, and Sponsor/Customer Audits
    • Experience Planning, Scheduling, Conducting, Reporting and Closing audit activitiesRequired Knowledge and Skills:
      • Considerable knowledge of quality assurance processes and procedures.
      • Strong knowledge of pharmaceutical research and development processes and regulatory environments.
      • Effective organization, communication, and team orientation and leadership skills.
      • Knowledge of word-processing, spreadsheet, and database applications.
      • Ability to influence and guide others.
      • Ability to manage costs effectively through appropriate resource allocation.
      • Ability to establish and maintain effective working relationships with coworkers, managers and clients.
      • Strong interpersonal skills.
      • Excellent problem solving, risk analysis and negotiation skills.Travel:
        • Up to 30 #LI-Remote #AmberPippinIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at - https://jobs.iqvia.com We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status Similar Jobs (1) Associate QA Director, Clinical Research locations Durham, North Carolina, United States of America time type Full time posted on Posted 30+ Days Ago About Us IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.
          
          To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q - Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.

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