Validation Specialist - Method

Liverpool Temporary
  • A rare opportunity to momethod validation
  • The business are a market-leading biopharmaceutical company

About Our Client

The client are a world-leading producer and developer of vaccines with their main manufacturing site based in Liverpool.

Job Description

As a validation specialist you will work within team to:

  • Maintain the compliant status of QC method validation life-cycle
  • Trouble shoot technical challenges with QC test methods
  • Execute method standardisation and robustness program
  • Aid in development of current and new test methods engaging with the latest testing technologies
  • Execute intra site method transfers and act as SME into regulatory filings/audits

The role will be predominantly lab based covering a range of analytical techniques relating to industry (UPLC, SDS PAGE etc).

The Successful Applicant

As the successful candidate you will have:

  • GMP knowledge learned from pharmaceutical industry (analytical biological background preferred)
  • Experience in a QC environment (1-2 years minimum)
  • Validation experience would be a bonus
  • Enthusiasm and a drive to develop you skillset
  • BSc in relevant scientific discipline

Although validation experience is desired, if you have strong GMP experience in a QC setting and are wanting to take the next step in your career please do apply!

What's on Offer

This is a rare and exciting opportunity to move into the field of method validation or to build on your existing experience within a market-leading biopharmaceutical business.

Jason Hines
Quote job ref
Phone number
+44 172 773 0102

Job summary

Contract type
Consultant name
Jason Hines
Consultant phone
+44 172 773 0102
Job reference