Administrative Assistant Intern

hace 5 días

Valencia, España Edwards Lifesciences A tiempo completo

Make a meaningful difference to patients around the world. Our **International Quality Program**is designed to help early-career professionals contribute to solutions that transform patient lives. We also believe in investing in the future of our talented people across the globe, including early career professionals seeking to explore and establish themselves within the medical device industry. As an **intern**with us, you'll thrive in a dynamic, patient-focused environment, influencing decision-making and optimizing product development to the highest standards of integrity and safety within the realms of **Quality and Supply Chain management**.

Location: Valencia, Spain

Duration: 6 months, 40hours/week

Start: 6th of October.

Your role will significantly influence various QA system processes:

- Perform administrative tasks that may include management, review and archiving quality records for various QA system processes: Field Corrective Actions, CAPA (Corrective and Preventive Actions), and Internal Audits.
- Prepare, manage, process and compile documents, ensuring they contain accurate information and in compliance with Good Documentation Practices (GDP) and ISO 13485 requirements.
- Collaborate with cross-functional teams, mainly Customer Service and Commercial Team, to request additional information, if required.
- May plan and execute meetings, under supervision.

What you’ll need:

- Enrolled University student (Bachelor/Master) of Information and Documentation or Business Administration (ADE) or any other related field, **interested in medical devices.**
- **Upper Intermediate English language skills necessary.**
- Full-time (40h/week) availability for min. 6 months.
- **Interest in quality assurance and the medical device industry.**
- Excellent analytical and problem-solving skills, with keen attention to detail.
- Knowledge in Office 365 (Word, Excel, Power Point etc.)
- Big plus: Basic understanding of quality standards such as ISO 13485 and Good Documentation Practices.

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