Internship - Quality HT Engineer 1

Celestica Inc.; Valencia; Presencial; EUR 6700 - 10.000; A tiempo parcial

Descripción de la vacante

Celestica Valencia is offering an Internship - Quality HT Engineer in Healthtech, focused on healthcare quality systems and regulatory compliance.

The role develops knowledge in ISO and FDA standards, supports documenting compliance, builds relationships across multidisciplinary teams, and helps improve the quality system while under supervision. English proficiency required, and the internship provides exposure to multinational processes.

Formación

• Read and write English required; spoken English desirable.
• Familiar with Windows software: Word, Excel, Gmail.
• Knowledge of mechanical, electrical, electromechanical, or bioengineering systems.
• Partial knowledge of ISO standards and how they operate.

Responsabilidades

• Support quality system documentation and regulatory compliance tasks.
• Assist in enforcing ISO and FDA standards within projects.
• Help build and improve the quality system with multidisciplinary teams.
• Develop skills in corrective actions, deviations, change control, and complaints.
• Generate reports to support system compliance and decision making.
• Work under supervision and with guidance from managers or SMEs.

Conocimientos

English proficiency (read/write)

Windows applications

Engineering fundamentals

ISO standards knowledge

Herramientas

Microsoft Office

Gmail

Descripción del empleo

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Internship - Quality HT Engineer 1

Date: Sep 4, 2026

General Overview

Summary

Summary

Area/Department: Healthcare Quality department
The Healthcare Quality department in Celestica Valencia is specialized in the assurance of the quality for current and new medical devices.
Customers go from worldwide multinationals to startups with innovative ideas.
The healthcare quality team is a young team in development with plenty of opportunities to grow.

Name of the position:
Quality Technical Support Healthtech student.

Quality Technical Support Healthtech: Internship

During the internship these skills will be developed:

• Work in a multinational company with their systems and procedures.
• Improve knowledge in ISO and FDA standards to documents occurrences of compliance/non-compliance with ISO/FDA Standards
• Ability to build internal and external relationships that require exchanging information and providing some explanations in a problem solving
• Help building and improving the quality system along with multidisciplinary teams
• Understand and develop skills for these different systems, Corrective actions, Deviations, Change control and Complaints.
• Learn the precise tools to follow up actions and achieve milestones.
• Earn trust and confidence to work under minimum Supervision.
• Generate reports that add value to the compliance of the system.
• Resolving tasks where considerable judgment and initiative are required in resolving problems and making recommendations. If any situation is not covered by standard processes, procedures and methods, it will be supported by the manager or subject matter expert.

Knowledge/Skills/Competencies:

• Read and write English is required to understand and create global procedures, spoken English desirable.
• Knowledge of personal computers and Windows applications. Word, Excel, Gmail.
• Knowledge of mechanical, electrical, electromechanical, or bioengineering-biomedicine systems and principals of operation.
• Partial knowledge of ISO standards and how they operate.

Typical Experience:
Student in practice

Notes

This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).
At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

COMPANY OVERVIEW:
Celestica (NYSE, TSX: CLS) enables the world’s best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud.Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.
Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

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