V.I.E Qualification & Validation Coordinator – Life Sciences

Description du poste

As a Validation and Qualification Consultant, your skills will support the projects of our partners involved in the production of pharmaceuticals or health-related products. You will play a central role in coordinating and executing the validation cycle to successfully complete projects within specified timelines. To achieve this, you will:

• Represent the Validation department in various projects.
• Design and implement the best validation strategy.
• Coordinate project planning with all stakeholders (production / QA / maintenance).
• Participate in risk assessment through the preparation of a « Risk assessment. »
• Contribute to the definition and drafting of Functional Specifications (FS) and Design Specifications (DS).
• Write protocols, coordinate and ensure the smooth conduct of tests (URS / FAT / SAT / IQ / OQ / PQ).
• Analyze and interpret results to write resulting reports.
• Develop training programs and coach operators in the field.
• Manage deviations related to validation runs and implement associated CAPAs.

Qualifications

• Curious to learn more about production equipment and/or manufacturing processes.
• Organized and meticulous in the preparation of your GMP documents.
• Communicative and enjoy interactions with different departments such as Production, Quality Assurance, and Maintenance.

Informations supplémentaires

What are the advantages of the V.I.E? 

• Getting professional experience abroad with the back-up and support of Business France and ALTEN Belgium 
• Becoming fluent in English & French languages 
• Finding the ideal environment for letting your atypical profile fully express itself 
• Receiving a tax-free allowance for the assignment you carry out 
• Discovering a new city and new cultures 
• Boost your career on the international stage! (if you doubt this, take a look at this testimonial https://www.alten-germany.de/en/2021/02/19/working-at-alten-gmbh-employee-portrait-engineering-consultant/