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As a Quality Assurance Specialist at Quality Enterprises Usa, you will play a crucial role in ensuring the quality and compliance of medicinal products used in clinical trials and managed access programs. Your primary responsibility will be to support the qualified person during release activities, collecting and checking documentation from various databases involved in the release process.
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 Quality Enterprises Usa and beyond.
- Support preparation and surveillance of Standard Operating Procedures (SOPs).
- Handle release timelines and coordinate with business functions.
Requirements
- Bachelor's degree in Sciences with 2 years experience in the pharmaceutical industry or a graduated apprenticeship within the field of medical, chemical, or pharmaceutical background.
- 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 Quality Enterprises Usa?
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Our purpose is to reimagine medicine to improve and extend people's lives, and our vision is to become the most valued and trusted medicines company in the world. We believe that our associates are the driving force behind our success, and we are committed to providing them with the opportunities and resources they need to grow and thrive.