Validation Engineer

  • Location: Wavre
  • Type: Contracting
  • Job #18899

Validation Engineer

Brabant Wallon – contracting 

Our partner is looking for a Validation Engineer to join its team. This international company is well-known for its pharmaceuticals and vaccines. 

What are your responsabilities ?

• You will be responsible for validation activities linked to changes controls (Management IOQ ,PQ validation, risk assessment , )
• You will be also responsible for the initiation/ coordination of change controls, linked to small projects related to equipment/process validation.
• eCC tasks follow up, KPI follow up, extract and tracking.
• You are responsible for ensuring and coordinating the support (planning, weekly validation, resources, cost) to change controls or projects.
• You will manage deviations and out of specifications: bring expertise and help in investigating and solving issues and associated CAPA linked to validation
• You will ensure coordination with all key players (local QA, Global QA, C&M, Streams rep,…).

Who are you?

• You hold a master’s degree in sciences/Engineering (Pharmacist / Sciences / Bio Engineer pharmaceutical…)
• You have minimum 3 years in the Pharmaceutical/Biotech industry with significant experience of GMP

• You have an expertise in validation, knowledge of International standards (CFR and Eudralex)

• You have strong leadership skills, a good decision maker, and have a critical mind
• You are fluent in French and English (both written and spoken)

What can you expect?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. 

You’re interested in this job? We kindly invite you to apply. Do you have any questions? You can contact [email protected] – 0472/44.83.18

 

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