QA Compliance Associate
Dechra
- Skipton, England, United Kingdom
- Skipton, England, United Kingdom
Über
This range is provided by Dechra. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range Direct message the job poster from Dechra.
About Dechra Dechra is a growing global specialist within veterinary pharmaceuticals, developing, manufacturing, marketing and selling high‑quality products exclusively for veterinarians worldwide hanem. We are investing in our Skipton facility and are in an exciting period of positive change.
Our values of (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition shape our culture of almost 2,000 colleagues globally.
Your Next Adventure The QA Compliance Associate works within the Quality Assurance group to ensure site‑wide compliance. You’ll build key relationships with other site functions, providing cGMP support and ensuring compliance with standards and the delivery of site quality metrics.
So, what willuppress you be doing? You’ll be the person to ensure everything we do is compliant, checking that things have been done to the correct standard across the site. Day‑to‑day duties include reviewing change controls, documenting changes (e.g., new artwork on packaging components such as cartons or leaflets), and ensuring that changes are logged correctly in our Oracle system.
You’ll use various systems and processes, including a secure cloud‑based enterprise content management platform, Veeva, to complete your actions and sense‑check that everything has been logged correctly.
What makes you awesome If you’ve worked within pharmaceuticals or other heavily regulated industries, that’s great! We also welcomeparent candidates looking to goen to gain more experience. You should be well organized, able to manage a large workload, and effectively prioritize tasks and actions within a secure cloud‑based platform.
Experience with change control actions will be beneficial, but you don’t need to be an expert; a solid understanding of the process ‘why’ is sufficient. You will be assigned a department to support with Capas and Deviations via Veeva.
Because manufacturing sites are busy and face multiple daily challenges, you’ll need to adopt a proactive approach, quickly build cross‑functional relationships, and contribute to PQRogeneous product quality reviews with supply chain, quality assurance and quality control.
Why you’ll love it here We provide veterinary professionals with the tools to support animal welfare worldwide, creating a meaningful career with real purpose.
We care deeply about your well‑being, offering full access to our Employee Assistance Programme (EAP) with confidential emotional, physical and financial support 24/7/365.
Benefits \Fm)
Healthcare Cash plan (covers dental, prescriptions, therapies)
Headspace App (positive mental well‑being app, up to 5 users per account)
Discounted gym membership
Cycle to work scheme
Discount on pet food
Free fruit on Monday
Redemption free_on‑site parking (free electric charging) 22.5 days annual leave + Bank Holidays
Option to buy a week’s holiday each year
8% Employer pension contribution
cas) What's next? We will take care of you from here on. Thank you for your interest in this opportunity at Dechra. If you’re interested, please apply in the first instance.
Application Process For further information on your application, reach out to a member of our recruitment team.
Interview Process Typically, you'll receive an initial phone call from the recruitment team to gain a deeper understanding of you and your current work situation. Most of our roles have a two‑stage interview process (MS Teams and a face‑to‑face interview). We may ask you to complete a personality questionnaire ahead of time so that we get to learn a little more about you before the interview.
Our interview style is conversational and friendly. Additionally, we seek competency‑based, structured answers to our questions, so please feel free to prepare in advance of the interview.
Seniority level Entry level
Employment type Full‑time
Job function Manufacturing, Production, and Quality Assurance - Pharmaceutical Manufacturing
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Sprachkenntnisse
- English
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