Validation Consultant
With over 20 years of experience in the field of Computerized Systems Validation and Training
Consultancy, we serve as one of the leading companies in the sector. We are looking for new
teammates to write our success story together with our strong staff and customer satisfactionoriented approach.

Scope of Work:
Taking part in Computerized Systems Validation Projects (ERP, MES, WMS, QMS etc.),
carrying out qualification and validation activities in accordance with GMP, FDA, Eudralex
and Ministry of Health regulations, applying the validation methodology and preparing the
necessary documentation.

Key Job Requirements:
• Preferably graduated from relevant engineering and science faculties (Chemical
Engineering, Bioengineering, Industrial Engineering, etc.),
• Preferably at least 2 years of experience in the pharmaceutical industry, familiarity with
GMP practices,
• Preferably knowledgeable about Quality Assurance / Quality Control Laboratory /
Production / Validation / Qualification processes,
• Able to use MS Office programs effectively,
• Fluent in English and Turkish,
• No travel restrictions and able to drive actively,
• Adaptable to flexible working hours,
• Male candidates must have completed military service,
• Open to development, analytical thinking and result-oriented,
• Prone to teamwork, open to positive and constructive communication,
• Experienced and responsible in project management,
• Will be able to adopt detailed documentation tracking and management.

For Applications; Please visit our website at https://www.convalgroup.com/career