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 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)
  
  

If this role is of interest to you, please apply now!

The candidate must have the rights to work in the location stated in the job advert.

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