Research & Development Quality Specialist

Research & Development Quality Specialist Job ID: REQ-10023125
Date: Sep 26, 2024
Location: Barcelona Gran Vía, Spain
Role Type: Hybrid Role, #LI-Hybrid
Summary As a Quality Specialist, you will contribute to improving and extending people's lives. You will work in a cross-country team to enable releases of medicinal products in clinical development at Novartis.
About the Role Key Accountabilities:
Support the qualified person during the release activities of medicinal products used in clinical trials and managed access programs.
Collect and check documentation from different databases involved in the release process.
Exchange with national and international stakeholders across Novartis and beyond (e.g. Country Organizations, Quality Assurance (QA) responsible functions globally, and external partners like local manufacturing sites).
Support preparation and surveillance of Standard Operating Procedures (SOPs).
Handle release timelines and coordinate with business functions.
Your Experience:
Bachelor's degree in Sciences or equivalent experience, including 2 years in the pharmaceutical industry, or a graduated apprenticeship within the field of medical, chemical, or pharmaceutical background, including 5 years in the pharmaceutical industry.
Excellent verbal and written communication in English.
Proficiency with Outlook, MS Word, Excel, PowerPoint, Teams, and other databases.
Interpersonal skills, with demonstrated ability as a collaborative team player and collaboration with different functions and country organizations.
Problem-solving and root cause identification skills.
Why Novartis?
Our purpose is to reimagine medicine to improve and extend people's lives. It is our associates that drive us each day to reach our ambitions. Be a part of this mission!
Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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