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Validation Engineer

  • Sector: Engineering
  • Contact Email:
  • Job Ref: 21321

Our Client is a global leader and manufacturer of injection-molded products for the medical device, pharmaceutical, healthcare and industrial markets as well as consumer packaging. They are currently expanding their current team to meet customer demand and are seeking an experienced validation engineer to join their team. This is a permanent position based in Co. Longford. The successful candidate is responsible for supporting all validation activities associated with the successful qualification of new tools / product introduction. Reporting to the Quality Manager thevalidation engineer will support the organization to achieve the new product introduction objectives.

Key Responsibilities:

  • Write and execute process validation protocols and reports for new product introductions and revalidations due to process /material improvements utilizing scientific / technical knowledge.

  • Developing and implementing solutions to sustain and improve the QMS.

  • Maintain and support compliance to ISO 13485 and ISO 14001 systems standards.

  • Participate in the site change control, ensuring that all changes to validated processes are effectively identified and implemented.

  • Generation of risk assessments, covering cleaning, validation, and process.

  • Review and execution of Factory Acceptance Testing and Site Acceptance Testing protocols.

  • Directly supports GMP and regulatory audits.

  • Prepare and deliver training modules as required.

  • Perform data analysis and make informed decisions / recommendations around conclusions reached from data analysis

  • Support continuous improvement through Lean Six Sigma methodologies.

  • Execution / development of change controls.

  • Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues e.g., FMEA, Fishbone diagrams, 5 why’s etc.;

  • Implement subsequent corrective action through the change management system.

  • Participate / lead cross functional teams including liaising with vendors on projects.

Qualifying Criteria:

  • Third level qualification in Engineering, Polymer Science, or equivalent Manufacturing experience.

  • Experience in statistical analysis (Minitab) / SPC / validations.

  • Excellent interpersonal, communication, influencing, and facilitation skills

  • A minimum of 2 years’ experience as a Validation Engineer within an Injection moulding or medical manufacturing environment.

Apply now to seize this excellent opportunity and advance your career in the Medical Device industry!

For more information please contact Cathal Herron:

(090) 645 0660