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Quality and Validation Specialist

Merseyside   •  Negotiable  •  Contract/Temporary, Full time

Quality and Validation Specialist


8 Month contract

Up to 60.00 per hour

Cpl Life Sciences are recruiting for a Quality and Validation Specialist to work for a company that derived from the expression 'securing health for all of us', They have a public health protection at its core. This reflects the promise of their parent company, founded in 1916 to save lives and protect the health of people.

As a Quality and Validation Specialist , you will Coordination and execution of equipment and computer systems qualification for QC equipment (plate reads, densitometers, UPLCs, TN analysers, particle size analysers) upon operating system upgrades.

Will involve the generation, execution and reporting of Installation and Operational Qualification protocols in line with project Validation Plans.

The specialist will be relied upon to understand the systems being updated and help configure the appropriate security features (user access, folder security etc) along with process owners and IT personnel.

The role will require a good level of communication with the project leads and associated Validation manager.

Potential for extension onto subsequent projects within QC and Secondary Manufacturing.


-Knowledge of working on Windows 7 and Windows 10 software

-Laboratory equipment validation experience is essential

-Upgrading experience is beneficial

-Minimum 2 years relevant experience

-Pharma Laboratory background or Laboratory equipment validation experience in other industries (e.g. Food or Beverages)

If this sounds like your ideal job, then wed love to see your application.

You can contact Zuzanna Erber, Consultant at CPL by email - zuzanna.erber@cpl.com

  • Agency: Cpl Life Sciences
  • Reference: JO-2205-492226
  • Posted: 10th May 2022
  • Expires: 7th June 2022

Cpl Life Sciences

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