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Search Results for Validation Specialist
Job Title. Location Salary Actions

Principal Engineer

Company: My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. Role: Principal Device Equipment Engineer Location: Newenham Court, Northern Cross, Malahide rd, Dublin 17 Benefits: Competitive salary, bonus, pension and full family healthcare Overview: The Princip...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Principal Engineer 		EU Not Disclosed

Principal Engineer

Company: My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. Role: Principal Device Equipment Engineer Location: Newenham Court, Northern Cross, Malahide rd, Dublin 17 Benefits: Competitive salary, bonus, pension and full family healthcare Overview: The Princip...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Principal Engineer 		EU Not Disclosed

Principal Engineer

Company: My client are a Pharma and Medical Device company developing combination products who have a global portfolio which includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. Role: Principal Device Equipment Engineer Location: Newenham Court, Northern Cross, Malahide rd, Dublin 17 Benefits: Competitive salary, bonus, pension and full family healthcare Overview: The Princip...

Location: Dublin, Dublin City Centre, Dublin Greater, Dublin North, Dublin South,
Principal Engineer 		EU Not Disclosed

Process Development Engineer

Job title: Process Development Engineer Location: Parkmore, Galway Company: My client are a medical device company developing a new and innovative device to support the heart. Heart support devices are used by interventional cardiologists to stabilize patients in times of acute heart failure (cardiogenic shock) or patients undergoing high-risk coronary procedures (high-risk PCI). Their objective is to overcome the limitations of current assist devices by providing interventional cardiologists with a more effective and less invasive device. Founded in 2018 as a Rad...

Location: Galway, Galway City,
Process Development Engineer 		Galway Not Disclosed
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Validation Specialist Career Profile

Validation Specialist

Validation is a Quality assurance process of establishing evidence that provides a high degree of assurance that a product, service, or system accomplishes its intended requirements. This often involves acceptance of fitness for purpose with end users and other product stakeholders. A highly technical position, the validation engineer completes or oversees all the calibration and testing of the various instruments and pieces of equipment. Validation is associated with all aspects of medical device industry from laboratories, manufacturing to computer software

Key Responsibilities of the Validation Engineer


  • The execution and completion of process, systems and equipment validations and revalidations in accordance with Validation Master Plans, schedules and Company policy.
  • Co-ordinate activities in all areas of validation
  • Prepare, execute and complete Validation Protocols and Reports, ensuring compliance to all relevant Quality Standards and Regulatory requirements.
  • As assigned, participate in cross functional teams to establish validation strategies and objectives to support the business
  • As needed, assist in providing related training and support.　
  • Provide guidance and support to all departments/staff as needed regarding related issues, ensuring compliance, as applicable, with ISO13485 and all other Quality Standards, Validation Regulations and Guidance Documents.
  • Maintain on-going understanding and knowledge of the latest regulatory requirements for validation in compliance with EU/U.S. regulations and guidance documents.　　
  • Monitor the progress of validation projects on a daily/weekly basis ensuring that there is continuous drive/focus on meeting schedules.
  • Participate in/Lead the review of validation practices in the company; monitor trends, and initiate improvement opportunities.