At a Glance
- Tasks: Join the Global Quality Team to enhance pharmaceutical safety and compliance.
- Company: IQVIA, a leader in life sciences analytics and technology solutions.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with potential for travel and collaboration across Europe.
- Why this job: Make a real difference in global health by ensuring quality and safety standards.
- Qualifications: Degree in life sciences with experience in Pharmacovigilance and stakeholder management.
The predicted salary is between 40500 - 49500 £ per year.
- Overview
- Company: IQVIA
Location: Primary Location: London, United Kingdom. Additional Locations: Amsterdam, Netherlands; Frankfurt, Germany; Warsaw, Poland.
- Job Type: Full Time
- Job ID: R
IQVIA is seeking a Global Quality Manager or Specialist for International Pharmacovigilance (IPV) Affairs CAPA Team, with the option to be based in the UK or anywhere in Europe.
This role is an individual contributor assigned to a designated Delivery Unit, sponsor, or business line.
Responsibilities
- Serve as a Member of the Global IPV Affairs Team.
- Act as a Subject Matter Expert for the IPV organization in your designated areas of responsibility.
Drive or support finding the most suitable and efficient solutions during discussions with different cross-functional teams and collaborate on reviewing and streamlining applicable procedural documents.
- Support the IPV organization on applicable operational tasks and ensure overall inspection readiness across IPV.
- Work closely with IPV Affairs members across regions to ensure a globally consistent approach for IPV.
- Own and coordinate Quality investigations/Quality Issues (QIs) and related records (CAPAs/Corrections) on behalf of IPV personnel – Originating from Self-Identified Quality Issues, Audit Findings, and/or Inspection Observations.
- Coach relevant stakeholders through the applicable QI processes.
- Support in writing investigations and conducting root cause analysis to ensure high quality, consistency, and accuracy of content.
- Collaborate with Medical Safety Teams/LSOs, Case Management team members, and other relevant stakeholders to identify appropriate solutions to mitigate non-conformances and prevent recurring issues.
- Maintain oversight of IPV-owned records and ensure timely completion and closure of records.
- Act as a Subject Matter Expert within IPV for all matters related to QI and CAPAs, providing advice or support on questions/concerns related to it.
- Review audit and inspection reports and support trending of observations to lead to overall global improvements.
- Support IPV in maintaining audit and inspection readiness for all IPV related activities.
- Support IPV Audit and Inspection RFI coordination – provide ETS Local, Regional/Global QI data as needed.
Education & Experience Requirements
- Medical, pharmaceutical, or life science degree with proven expertise and experience in the pharmaceutical industry and experience in Pharmacovigilance.
- Minimum of 1 year’s experience in a position within Pharmacovigilance plus 6-8 years of related experience.
- Excellent stakeholder management, negotiation skills, and coaching people in influencing internal and external partners.
- Task-oriented with proven experience in the delivery of high-quality work as part of a multi-disciplinary team.
- In-depth understanding of vigilance systems and processes; knowledge of or experience with International Pharmacovigilance and compliance regulations and guidelines is an advantage for this role.
- Demonstrable insight into the development of regulatory requirements with knowledge of Global aspects of drug/cosmetics/devices safety, including international reporting requirements and relevant country-specific variations.
- Excellent computer-based application skills.
- Fluent communication skills in English; any additional language is a plus.
- Location & Travel
- Global Office-based role from any Pharma office in the correspondent region. Remote work is possible.
- Up to 25% travel might be required.
- About IQVIA
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
How to Apply
Click the “APPLY NOW” button to submit your application.
Global Quality Specialist / Manager at IQVIA in London employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IQVIA, Inc. that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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