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Validation Roles in Pharma Industry = Need Genuine Profiles
Senior Validation Engineer with minimum 5 years of experience in developing the Life Cycle documents and IOPQ protocols, executing the protocols, addressing discrepancies/deviations, preparing summary reports and compiling final report packages, etc.
for Aseptic Liquid Fill equipment and systems that include autoclaves, vial washers, depyrogenation tunnels, fillers, stoppers, lyophilizers, parts washers and critical utilities (e.g., WFI, Clean Steam, Clean Compressed Air, etc.).
Packaging Equipment CQV
Candidates need to have experience in equipment such as Seidenader, Bausch+Strobel, Harro Hofliger, Fargo, Dividella, Pester (Syringe Assembly Machine, Semi-Automated Pen Assembly Machine, Blister Former, Cartoner and Inspection Machines).
Must be able to get up to speed as soon as possible and work independently. Must have a clear understanding of System Life Cycle documentation and know how to find the answers.
Must have the experience to be able to identify things that are not completed and know what to ask to reach the goal. Minimum 5 years of CQV Experience
Parenteral/ Aseptic Processing CQV
Candidates need to have experience in the qualification of Commercial Filling Line Equipment and Isolators (SKAN, Bausch+Strobel, GEA, VarioSys).
Must be able to get up to speed as soon as possible and work independently.
Must have a clear understanding of System Life Cycle documentation and know how to find the answers.
Must have the experience to be able to identify things that are not completed and know what to ask to reach the goal.
Minimum 5 years of CQV experience
Generation of protocols, summary reports, and protocol exceptions
Scheduling and execution of qualification activities
Qualification data collection and analysis against acceptance criteria
Introduction: My name is Tish Haag, I am a excited, delightful, curious, beautiful, agreeable, enchanting, fancy person who loves writing and wants to share my knowledge and understanding with you.
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