Validation Engineer

Validation Engineer   Reference: TPS065  
SALARY Negotiable   LOCATION Dublin, Ireland
JOB TYPE Contract (12 months)   DATE POSTED 08/01/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
Client; Systems Integrator focused on Process Automation Delivery of Process Automation Solutions to Global Brands.

End client focus; Distilleries | Breweries | Blending Plants | Food Production | BioPharma

Job Title; Validation Engineer

Responsibilities;  Ensuring that all manufacturing processes, packing operations, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements and GMP regulatory requirement. Must have the presence to promote the company image and ensure that this is enhanced by the successful implementation of systems.
This will be an interesting and varied role, and the opportunity to progress within the team will be available to the right candidate. Produce project documentation suite such as design documentation and test specifications and expected to review documents produced by junior engineers.
Essential Skills;

  • At least 5 years experience in Validation (ComputerSystem/Process/Project/Equipment/Cleaning etc.) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries).
  • Strong cGMP, GAMP and GxP knowledge with knowledge of FDA 21 CFR Part 11, Annex 11 regulation.
  • Demonstrated understanding and hands-on experience generating and reviewing validation lifecycle documents.
  • Ability to discuss technical aspects of validation and GxP testing with clients.
  • Strong attention to detail regarding documentation is a must.
Charlie Burgess 02081236574 Recruiter Automation UK
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