Validation Engineer - Remedica Ltd

Τίτλος θέσης: Validation Engineer

Role: The purpose is to ensure that all systems (productions equipment, facilities and utilities) are commissioned and qualified in accordance with the requirements of Current Good Manufacturing Practices (cGMP) and maintain their qualified status throughout the systems lifecycle.

Duties and Responsibilities

• Organizing and executing qualification activities
• Preparing or assisting in preparing reports relevant to qualification activities as and when needed
• Maintaining accurate and up-to-date records and drawings relevant to qualification data/activities
• Ensuring that all activities of the department comply to the established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP).

Qualifications 

• Degree in Engineering, Chemical Engineering or any other relevant field

 Required Skills

• High attention to detail
• Organized and methodical way of thinking
• Ability to work collaboratively in a team
• Excellent written and verbal communication skills
• Excellent command of the English Language
• Knowledge of Microsoft Office

An attractive remuneration package depending on qualifications that includes 13th and 14th salary, Provident Fund, medical cover, gym access, subsidized meals etc are offered. Interested candidates should apply online through Remedica’s website www.remedica.eu

Ευχαριστώ εκ των προτέρων. Παραμένω στην διάθεση σας για τις οποιεσδήποτε διευκρινήσεις.

Kind regards,