About the Role
This role offers the opportunity to work with a medical device client based in Co Cork.
Main Responsibilities:
* Owning and supporting validation activities according to regulatory requirements.
* Ensuring all process validation executions are completed as planned.
* Performing software validation executions, including testing and verification.
* Resolving problems encountered during validation activities.
* Maintaining consistency in validation/qualification approaches across systems and projects.
* Providing guidance on the preparation and execution of validation activities.
* Staying up-to-date with GMP requirements for site-wide compliance with regulatory bodies.
* Managing the validation system, including conducting periodic reviews.
* Participating in change control processes for manufacturing process and facility modifications.