Summary:

The Work we do at IQVIA impacts lives all over the world. At IQVIA, the Largest Human Data Science Company in the world, we accelerate innovation for a healthier world.  Come and join us to help our customers and partners do extraordinary things for healthcare!

The IQVIA Enterprise QA 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, 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.

The workplace is remote and located in the United Kingdom (home-based).

Purpose:

The Senior QA Auditor will plan and conduct independent audits to assess compliance with regulations, guidelines, and operating procedures.  Prepare and distribute reports of findings to supervisor, operations staff, management, and customers. Provide consultation in interpretation of regulations, guidelines, policies, and procedures.  Support management in promotion and assessment of compliance to regulations, guidelines and corporate policies.

Summary of Responsibilities:

• Plan, schedule, conduct, report and close audit activities in any of the countries involved with IQVIA contracts to assess compliance with applicable regulations/guidelines, customer requirements, IQVIA SOPs and project specific guidelines/instructions

• Evaluate audit findings and prepare and distribute reports to operations staff, management, and customers

• Provide interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures

• Provide consultation to customers and monitors in interpretation of audit observations and formulation of corrective action plans

• Manage Quality Issues

• Present educational programs and provide guidance to operational staff on compliance procedures

• Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closures for quality events arising from Quality Issues, Audits, Inspections or during similar QA activities

• Provide quality assurance consultancy activities and projects for clients within budget and established timelines

• Evaluate policies and procedures for compliance with applicable regulations/guidelines and provide recommendations to management for continuous process improvements

• Host audits/inspections, Ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections

• May perform GLP Archivist duties where needed

• Manage/oversee quality events updates in eQMS and/or Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle

• Lead/collaborate/support in QA initiatives/projects for quality, process improvements

• Assist in training of new Quality Assurance staff

Required Education and Experience:

• Previous or current experience in a pharmaceutical, biotech, CRO, or other regulated area

• Min 1 year of experience in Quality Assurance

• CAPA and GCP experience

• Ideally Life-science/Pharmaceutical degree

Required Knowledge, Skills and Abilities:

• Knowledge of word-processing, spreadsheet, and database applications..

• Extensive knowledge of pharmaceutical research and development processes and regulatory environments..

• Knowledge of quality assurance processes and procedures..

• Strong interpersonal skills..

• Excellent problem solving, risk analysis and negotiation skills..

• Strong training capabilities..

• Effective organization, communication, and team orientation skills..

• Ability to initiate assigned tasks and to work independently..

• Ability to manage multiple projects..

• Ability to establish and maintain effective working relationships with coworkers, managers and clients.

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IQVIA 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