Cleaning Validation Engineer
14 hours ago
Cleaning Validation Engineer - Ireland, Carlow - 11 Month Contract
Do you want to be involved with exciting pharmaceutical projects?
Our pharmaceutical client, a leader in veterinary vaccines with the largest industry centre worldwide and a Centre of Excellence employing over 1000 people, is looking to add a Cleaning Validation Engineer to their team.
Essential Duties and Responsibilities:
Design, author, review, approve, and execute qualification/validation documentation and cycle development studies in line with the standard approval process.
Design, author, review, approve, and execute change controls.
Resolve technical issues during study execution.
Engage with Production, Maintenance, and Quality teams during Cycle Development & Performance Qualification activities.
Provide technical input into quality investigations by authoring, reviewing, and approving reports.
Perform root cause analysis of system failures using standard tools and methods.
Ensure compliance through documentation, risk assessments, corrective actions, and participation in audits and inspections.
Support regulatory audits and submissions as needed.
Promote a safe and compliant culture within Carlow.
Perform other duties as assigned.
Desirable Experience:
Experience in cleaning validation, including CD & PQ of mobile vessels (CIP) and parts washers (COP), recipe development, verification, cleanability, and recovery studies using TOC, ICP, and swab methods.
Experience operating as an individual contributor in a GMP manufacturing setting.
Relevant technical qualifications in Pharmaceutical, Biological, Chemical sciences, or Engineering, with a proven track record of excellence.
If this role interests you, please apply now
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