Process validation engineer (medical device)

• Develop and oversee of equipment documentation and process validation (IQ,OQ,PQ)
• Performing and document process validation activities (PV) including protocols and reports.
• Define and write engineering documents.
• Part of a team of transferring of new products and processes into the production line.
• Monitoring and testing equipment
• Analyzing and documenting test results

Qualifications (Education, Skills, and Experience; Required):

• Mechanical or Medical Engineer, as least 5 years of experience at R&D/ Engineering department in medical device companies.
• Knowledge of medical validation process.
• Communicate with technical and non-technical team members effectively.
• Good team player.
• Quick learner
• English - Fluent reading and writing