Role

The role of Validation Engineer is to ensure that Manufacturing and Packaging Equipment, GMP areas and Utilities are commissioned and qualified in accordance with the requirements of Current Good Manufacturing Practices (cGMP) and maintain their qualified status throughout systems lifecycle.

Duties and Responsibilities

• Following validation master plan, for the scheduling, and execution of qualification activities for Manufacturing and Packing Equipment, GMP areas and Utilities.

• Developing documentation related to validation activities such as protocols, risk assessments and compliance reports.

• Periodic testing the proper functioning of systems and resolving any issues, including facilitating corrective measures or improvements based on results analysis and evaluation.

• Analyzing data from validation tests to determine whether systems meet required criteria and specifications.

• Maintaining databases for tracking test results, validation activities and validated systems.

• Ensuring that commissioning and qualification activities comply with the established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP).

Qualifications:

• University Degree in Engineering.Mechanical, Electrical, Chemical Engineering or any other relevant field

• Industrial experience will be considered as an advantage.

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

Benefits:

• 13th and 14th salary

• Provident Fund

• Group Medical Plan

• Discount scheme

• Gym Access

Interested candidates should apply via email: careers@remedica.com.cy