Senior Cleaning Validation Engineer

3 days ago

Carlow, Ireland Life Science Recruitment Ltd Full time
11 month contract Senior Validation Engineer - Cleaning On site Carlow AMC22966 We are currently hiring for a Senior Validation Engineer role with a rapidly expanding biopharmaceutical manufacturer based in Carlow.

In this role you will support Cleaning validation on site.

The ideal candidate will have 5+ years of experience in validation of sterile fill finish processes and equipment including extensive cleaning validation experience Responsibilities Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process.

Design/Author/Review/Approve/Execute Execution/development of change controls.

Resolving technical issues encountered during study execution.

Engagement with Production, Maintenance and Quality representatives in the assigned area of operations during execution of Cycle Development & Performance Qualification activities.

Technical input into quality notification by authoring/reviewing/approving investigations.

Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues.

Support continuous improvement through Lean Six Sigma methodologies.

Serve as validation representative for cross functional projects and represent the validation team at global technical forums Drive compliance of Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (c GMP) in the performance of day-to-day activities and all applicable job functions, ensuring consideration of the impact on GMP and compliance and decisions made.

Accountable for compliance via documentation completion, risk assessments, closing out corrective actions, participation in audits and inspections and proactively highlighting any issues around compliance Supporting regulatory audits and submissions as required.

Requirements Relevant technical degree Experience in cleaning validation including but not limited to CD & PQ of mobile vessels (CIP) and parts washers (COP) including recipe development & optimisation, cleaning verification, cleanability and recovery studies using TOC, ICP & swab methods, acceptable residual limit determination, worst case soil matrices & strategy development Exception / Deviation Management and Change Control.

Demonstratable experience of leading technical related projects.

Ability to analyse and interpret complex data, and link to equipment performance and out of specification findings as appropriate.

Report, standards, policy writing skills required.

Equipment and process validation.

Sterile Fill-Finish processes and equipment Desirable Knowledge of process monitoring systems, automation systems (Delta V), operational intelligence & data systems (Pi System) within a GMP manufacturing environment Evidence of continuous professional development Ability to analyse and interpret complex data, and link to equipment performance and out of specification findings as appropriate.

Knowledge and experience of the below areas will be considered advantageous: Filter Validation CCI qualification Shipping Qualification Equipment Periodic Validation Equipment Validation Lifecycle Project Management Skills/Qualification Autoclave/SIP Sterilisation Validation Dry Heat Sterilisation Isolator VHP/HVAC Qualification Controlled Temperature Units/Equipment Qualification Vial and Syringe Processing Technologies Get in touch with Angela Mc Cauley or apply today

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