SKILLS BRIEF:

• Managing & coordinating the preparation, review & approval of Validation Master Plans
• Generate, execute and review validation protocols and associated reports for related equipment and processes.
• Managing & coordinating of all validation strategies & deliverables
• Managing & coordinating the preparation, review & issuing of validation protocols & reports
• Managing & coordinating validation documentation (risk assessments, traceability matrices)
• Managing & coordinating the review & approval of specifications associated with Equipment & Processes.
• Managing & coordinating routine Internal Quality Audits of the facility to ensure compliance & be proactive in resolving issues that may arise.
• Provide technical direction & hands-on assistance for testing projects

THE ROLE:

• Equipment Validation Engineer
• Kilkenny
• Onsite
• Contractor or Permanent opportunity

ROLE BRIEF:

The successful candidate will focus on the validation activities for a range of equipment solutions within a regulated Pharma environment.
You will both have responsibility for a number of activities and pieces of equipment while also supporting the wider Validation function and ensuring Validation activities are closed out in line with the Validation Master Plans.