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QC Stability Associate

Please Note: The application deadline for this job has now passed.

Job Introduction

Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra Pharmaceuticals PLC.

Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.

Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2000 colleague globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business

The Opportunity 

As part of the Quality Control team, the Stability Associate maintains, co-ordinates and controls the site’s stability program, providing technical knowledge of capabilities, controls and trial status’ for the department.

Role Responsibility

The Challenge

So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including:

  • To control and maintain the stability management program, including:
    • New sample requests, full lifecycle management of samples, including their set-down, availability for testing and subsequent destruction
    • Pull date management and sample retrieval
    • Samples submission to external testing houses
    • Trend analysis, including the reporting of OOS/T results
    • Author Stability Protocols and Reports
    • Stability Cabinet / Chamber monitoring
  • Undertake Laboratory Investigation Reports (LIRs), Deviations, Change Controls, CAPAs, Due Date Extension Requests and Effectiveness Reviews for related work.
  • Collate and report KPIs and other quality-indicating metrics

The Ideal Candidate

About You

Here at Dechra we pride ourselves on being an inclusive employer and we embrace candidates from all walks of life. We’re particularly keen to here from those who have/are:

  • 2 years’ experience working in a Quality Control / Assurance department within a GMP-compliant environment.
  • Keen attention to detail
  • Confident with both written and verbal communication to a variety of stakeholders as well as report writing.

About the Company

About Your Application

All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we’re looking for. Should you not hear back from us within 28 days please don’t be too disappointed – we may keep your CV on our database for any future vacancies which may be suitable and we encourage you to keep an eye on our careers site. For any questions or queries, please contact us at recruituk@dechra.com

Dechra Pharmaceuticals PLC

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