Cleaning Validation Engineer - Life Science - Cork - 12-Months+ Contract
We have a great opportunity for Cleaning Validation Engineers to join our client, a research-based biopharmaceutical company, on their journey of discovering, developing, and commercialising innovative medicines and researching and developing antiviral drugs used in the treatment of HIV / AIDS, hepatitis B, hepatitis C, influenza, and COVID-19.
Responsibilities include, but are not limited to, the following :
- Generation of Validation Impact Assessments (“VIA”)
- Review of Change Controls
- Generation of Process Validation Plans
- Generation of Cleaning Validation Plan(s)
- Update of Cleaning Validation and Process Validation documentation impacted by the changes
- Cleaning Technical Assessment
- Process Flow of Products / Equipment at the Company
- Cleaning Validation Matrix
- Generation of Process Performance Qualification (“PPQ”) and Process Validation (“PV”) Protocol(s)
- Execution of Process Validation Protocol (PPQ / PV) activities
- Conduct training on PPQ / PV Protocols
- Generation of PPQ and PV Reports
- Review / Approval of project Failure Mode Effect Analysis (“FMEA”) / Technical Assessments as required
- Performance of cleaning validation as per Cleaning Validation Plan(s) / Protocol(s)
- Any other ad hoc project deliverables
Requirements :
Conduct training on PPQ / PV ProtocolsGeneration of PPQ and PV ReportsReview / Approval of project Failure Mode Effect Analysis (“FMEA”) / Technical Assessments as requiredPerformance of cleaning validation as per Cleaning Validation Plan(s) / Protocol(s)If this role is of interest to you, please apply now!
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