Job Description DEPARTMENT: Quality Department REPORTING TO: Validation Quality Lead Individual Contributor or People Manager: Individual Contributor OBJECTIVES OF POSITION: To support validation activities in a Medical Device regulated environment.
RESPONSIBILITIES: Support validation activities in a Medical Device regulated environment.
Support Process, Software and Facility Val i dation in Fermoy.
Assist with resolution of Problems encountered during validation.
Become fully conversant and up to date with GMP requirements for site-wide regulatory body compliance.
Participate in change control processes for manufacturing process and facility modifications.
Quality: Assure ongoing compliance with quality and industry regulatory requirements.
Health