Validation Engineer
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