Description
I have an immediate job opening for a Validation Engineer with a leading medical device company based in Cork. This is an initial 12 month fixed term contract position and is a fantastic opportunity to join a global company throughout an exciting growth phase.Responsibilities:
- Develop and execute facility, process and equipment validations with regulatory, corporate requirements and business requirements.
- Perform process improvement studies, complete process validations and Risk Management to improve quality rates and cycle times for IOL product line.
- Review for compliance to Quality System requirements, project documentation including validation and software documents.
- Use knowledge of statistics to assist with validation developments and process improvements.
- Maintain/Support the Risk Management and Validation System in compliance with International requirements.
- Adhere to inhouse H&S and environmental requirements.
- Ensure continual Quality System compliance by adherence to established and evolving company QS requirements
- Knowledge of FDA, medical device, GMP and validation requirements.
- Experience in equipment and process validations.
- Knowledge of Statistics
- Skills: Project management, problem solving, statistical analysis and word processing.
- Report writing expertise and highly developed people skills
Requirements:
- Bachelors degree from an accredited institution in a technical discipline
-4 years technical & validation experience
This company offers excellent opportunities for career progression if you are interested in hearing more about this fantastic opportunity please apply directly to this advert for immediate consideration.