Research & Development Quality Specialist Job ID: REQ-10023125Date: Sep 26, 2024Location: Barcelona Gran Vía, SpainROLE TYPE: Hybrid Role, #LI-HybridSummary 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 a science-based field, including 2 years of experience in the pharmaceutical industry, or a graduated apprenticeship within the field of medical, chemical, or pharmaceutical background, including 5 years of experience in the pharmaceutical industry.Excellent verbal and written communication skills 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.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.#J-18808-Ljbffr