Job Title: Validation Engineer Opportunity
This is an exciting opportunity to join a leading healthcare manufacturing company and contribute to the growth of our operations in Waterford, Ireland.
Key Responsibilities:
* Create and execute validation documentation and coordinate validation activities for injection moulding, assembly processes, and facilities within the quality management system.
* Develop and implement validation plans, protocols, reports, and amendments of the Quality Management System, ensuring compliance with regulatory requirements within the Medical Device and Pharma Sector.
* Generate quality documentation in conjunction with validation activities.
* Liaise with cross-functional teams to drive validation initiatives into operational activities.
* Develop validation projects and master validation plans.
* Ensure ongoing compliance with GMP practices, recording of events, and processes.
Required Skills and Qualifications:
* Degree in Engineering or Science discipline.
* 1-3 years' experience in a Validation or Quality engineering role.
* Knowledge of process validation and capability, ideally with method validation and process characterization experience.
Benefits:
* Collins McNicholas is an equal opportunities employer. We welcome applications from qualified candidates who are passionate about delivering high-quality results in a dynamic environment.
Our company offers a collaborative and supportive work environment, where you can grow and develop your career in a rapidly evolving industry.