Quality Assurance Specialist for Clinical Trials

hace 1 mes


Barcelona, Barcelona, España Novartis Farmacéutica A tiempo completo

Job Summary

As a Quality Specialist at Novartis Farmacéutica, you will play a crucial role in ensuring the quality and safety of medicinal products used in clinical trials and managed access programs. You will work closely with cross-functional teams to enable the release of these products, collaborating with national and international stakeholders to ensure compliance with regulatory requirements.

About the Role

Key Responsibilities:

  • Support the qualified person during 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.
  • Support preparation and surveillance of Standard Operating Procedures (SOPs).
  • Handle release timelines and coordinate with business functions.

Requirements

• 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.

What We Offer

At Novartis Farmacéutica, we are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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