Cleaning Validation Engineer
3 weeks ago
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.
- 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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