IQVIA

Quality Assurance Manager (QA)

Company
IQVIA
Location
Warsaw
Posted
14 Apr 2021
Closes
13 May 2021
Ref
R1199573
Discipline
Quality
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

PURPOSE

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 support to management with 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 . Manage the quality assurance oversight of projects, assignments, training and staff.

Main responsibilities:

  • Prepare for and/or host customer audits, mock regulatory inspections, and regulatory facility inspections as needed
  • Provide guidance, interpretation, support, training, and key input to development groups for consultation and interpretation of regulations, guidelines, corporate standards, and policies.
  • Oversee and participate in the documentation, reporting, and closure of compliance issues.
  • Organize and deliver training to other IQVIA departments concerning the activities of Quality services, results of activities, quality initiatives, GXP etc.
  • Ensure the follow-up of major and critical audit findings to ensure that appropriate actions have been taken and have adequately resolved the issues identified
  • Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements
  • Serve as author of Quality Assurance Standard Operating Procedures ( SOPs) as assigned.
  • Advise Quality Assurance management on system audit needs.
  • Ensure the Quality Assurance database is maintained and up-to-date to reflect the status of audits being scheduled, auditor assignment and audit reporting and/or follow-up status.

The ideal candidate should have:

  • Typically requires 3 - 5 years of prior relevant experience.
  • Direct experience Hosting audits and inspections
  • GXP knowledge.
  • Knowledge of word-processing, spreadsheet, and database applications
  • Extensive knowledge of pharmaceutical research and development processes and regulatory environments.
  • Considerable knowledge of quality assurance processes and procedures.
  • Strong interpersonal skills
  • Excellent problem solving, risk analysis and negotiation skills.
  • Exceptional training capabilities.
  • Effective organization, communication, team orientation, and leadership skills.
  • Ability to work independently with initiative.
  • Ability to manage multiple projects
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients..

**Home based**

At IQVIA, 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. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.