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Open nowPosted 15 hours ago

Werfen template

Actual Talent97 open roles

Where
Lliçà d'Amunt, Spain
Work mode
On site
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Your applicationOpen nowWerfen templateActual Talent · Lliçà d'Amunt, Spain

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The clock on this job

Early applications get read.

8.2% of postings close within 7 days. Measured by our own scanner across the market. Actual Talent postings stay open a median of 5 days.

Share of postings closed within
  1. 1.9%1 day
  2. 3.8%3 days
  3. 8.2%7 days
  4. 15.2%14 days
  5. 34.1%30 days
This job: posted 15 hours ago

Actual Talent median: 5 days open

The posting

Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain.

We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. We operate directly in 30 countries, and in more than 100 territories through distributors.

Our Headquarters are in Barcelona, Spain and our Technology Centers are located in the United States and Europe. Worldwide sales exceeded €2.2 billion in 2024, and our workforce is more than 7,000 strong.

JOB SUMMARY

We are seeking a student interested in the field of Quality and Validation to join our Quality team. The selected individual will provide support for activities related to the validation of facilities, equipment, and production processes, as well as document management and risk analysis associated with products and processes within a highly regulated environment.

This position offers an excellent opportunity to gain practical experience in quality systems, validation, and risk management at a leading healthcare company.

Responsibilities:

· Collaborate on the preparation and review of validation documentation for facilities, equipment, and production processes.

· Support the execution and monitoring of validation activities, ensuring compliance with established quality standards.

· Participate in projects and initiatives aimed at continuous improvement and the optimization of department processes.

· Contribute to the identification, assessment, and management of risks associated with validation activities.

· Review technical documentation related to product design.

· Assist in analyzing risks arising from modifications or changes to product design.

· Track and monitor risk documentation currently undergoing updates.

· Collaborate with various areas of the organization to ensure compliance with quality and regulatory requirements.

Requirements

· Undergraduate or Master’s student in Biomedicine, Biochemistry, Pharmacy, or related fields.

· Interest in quality systems, process validation, and risk management.

· Analytical skills, attention to detail, and a focus on continuous improvement.

· Strong organizational and document management skills.

· Upper-intermediate level of English.

· Proficiency in Microsoft Office.

Working hours: Part-time.

Start date: November 2026.

Work arrangement: On-site position.

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