SonicJobs Logo
Login
Left arrow iconBack to search

Senior Validation Officer

WALKER COLE INTERNATIONAL LTD
Posted 5 hours ago, valid for 16 days
Location

Leeds, West Yorkshire LS12 5HR, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

info
  • Walker Cole International is seeking a Senior Validation Officer for a leading pharmaceutical manufacturer in West Yorkshire.
  • The role involves leading validation activities, authoring protocols, and supporting tech transfers in a GMP environment.
  • Candidates should have significant experience in a GMP-regulated pharmaceutical setting and a degree in a scientific or engineering discipline.
  • The position offers a salary of £45,000 to £55,000 per year, depending on experience.
  • This is an excellent opportunity for those looking to step into a supervisory role within the pharmaceutical industry.

Walker Cole International is currently supporting a leading pharmaceutical manufacturer in their search for a Senior Validation Officer to join their Quality Assurance function at their site based in West Yorkshire.

The company specialises in the manufacture of patient-centric medicines and is committed to the development and global supply of novel-dose pharmaceuticals. This role offers the opportunity to play a key part in validation projects and continuous improvement initiatives across manufacturing and quality operations.

Key Responsibilities:

  • Lead and execute validation activities in line with GMP regulations and company SOPs.

  • Author and review validation protocols, reports, and risk assessments (including FMEA and root cause analysis).

  • Act as deputy to the Validation Manager and provide mentorship to junior validation team members.

  • Support the tech transfer of new products, ensuring all process and cleaning validation requirements are met.

  • Monitor and report on key Quality metrics, and contribute to regulatory submissions and audit readiness.

The successful candidate will have:

  • A degree (or equivalent experience) in a scientific or engineering discipline.

  • Significant experience in a GMP-regulated pharmaceutical manufacturing environment.

  • Proven track record of authoring and executing validation protocols.

  • Familiarity with quality systems, risk assessment methodologies, and regulatory expectations for validation.

This is an excellent opportunity to step into a supervisory role and contribute to the development and validation of essential pharmaceutical products.

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.