Practicante de Calidad

Requirements

• Students or recent graduates in Engineering.
• Proficient in Microsoft Office.
• Availability to work (Monday-Friday).
• Advanced English.
• Beware of scams online or from individuals claiming to represent Convatec
• A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.
• If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at careers@Convatec.com .
• Equal opportunities
• Notice to Agency and Search Firm Representatives
• Already a Convatec employee?
• If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Additional Information

About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec's revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com The Quality Engineering Intern provides support to the Quality department in activities related to ensuring regulatory and compliance requirements for products and processes. The intern participates in the implementation and maintenance of the Quality Management System (QMS) in accordance with medical industry standards such as ISO 13485, FDA 21 CFR Part 820, and Good Manufacturing Practices (GMP), contributing to product quality, safety, and effectiveness.

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