Review and analyze CSV parts from our client;
Realize on field Gemba in order to check the conformity of the project and recommendation;
Take Corrective Action / Preventive Action regarding CSV aspects;
Be a guide for our client regarding regulatory compliance and computer validation;
Assure the link between Altran and the client regarding all CSV aspect.
You are an “Innovation Maker” and you want to put your engineering , science and business skills to use to create solutions. You like to share your knowledge with likeminded engineers and you know how to take initiative .
Master degree in (Bio-)engineering, computer science or related domains,
Fluent in English and French or Dutch,
At least 3 years of relevant experience in CSV in a pharmaceutical industry (as FDA part 11);
You will be recruited by Georges & Isabelle, don’t hesitate to contact them & send them your CV: firstname.lastname@example.org - Isabelle.Thysens@altran.com
Discover more about your career on www.altran.be/careers