QA Compliance Associate

Dechra Group; Skipton; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global veterinary pharmaceutical company is looking for a QA Compliance Associate based in Skipton, UK. In this role, you'll ensure site-wide compliance with standards, manage change controls, and contribute to Product Quality Reviews. The ideal candidate will possess strong organizational skills and a proactive approach, with preferably some experience in regulated industries. The company offers a comprehensive benefits package, including healthcare plans and 22.5 days of annual leave.

Benefits

Healthcare Cash plan

Headspace App access

Discounted Gym Membership

Cycle to work scheme

Discount on pet food

Free fruit on Mondays

Free on-site parking

22.5 days annual leave

8% Employer pension contribution

Qualifications

• Experience in regulated industries is preferred, but not mandatory.
• Ability to manage a large workload and prioritize tasks effectively.
• Understanding of change control process beneficial.

Responsibilities

• Ensure site-wide compliance by checking standards.
• Document and manage change controls and related processes.
• Contribute to Product Quality Reviews and manage the PQR system.

Skills

Organizational skills

Proactive approach

Understanding of compliance processes

Tools

Oracle

Veeva

Job description

Vacancies

QA Compliance Associate

Job Introduction

QA Compliance Associate 0800 - 1630 hrs, Mon‑Fri (with every second Friday off). Site‑based.

A little about us: 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. It’s a great time to join our modern Skipton facility, and further investment for the Skipton site means that we’re in an exciting period of positive change for the business.

Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2000 colleagues 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.

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 to ensure compliance with standards and the delivery of site quality metrics.

So, what will 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, you’ll look at change controls and document what the change is. This could be new artwork, for example, on the packaging components such as cartons or leaflets and packing records, etc. Your team facilitates overseeing the change and making sure it can go ahead.

You’ll use various systems and processes to complete your day‑to‑day actions and sense‑check that everything has been logged correctly on our Oracle system.

What makes you awesome

If you’ve worked within Pharmaceuticals before or other heavily regulated industries, then great! Equally(dr), we’ll still love to hear from you if you’re looking to gain more experience in this area. You’ll need to be well‑organised, manage a large workload, and effectively prioritise a range of tasks and actions within our secure cloud‑based enterprise content management platform, Veeva.

Experience with change control actions will stand you in good stead, but you don’t need to be a subject‑matter expert in this area; more of an understanding of the ‘why’ behind the process. You’ll be assigned a department to support with Capas and Deviations via Veeva.

You won’t always be able to get hold of the right people or find the answers you need right away. Manufacturing sites are very busy and face multiple challenges daily. Because of this, you’ll need to adopt a proactive approach to the working day and build relationships quickly across cross‑functional teams. You’ll actively contribute towards PQR Product Quality Reviews with Supply Chain, Quality Assurance and Quality Control involved, managing the PQR system and your actions as well.

Why you’ll love it here

We provide veterinary professionals with the tools to support the welfare of animals worldwide. A true career with real purpose, that’s something you can proudly shout about.

Benefits

We also care deeply about you; you’ll have full access to our Employee Assistance programme (EAP) which ensures you have confidential emotional, physical and financial wellbeing support 24/7, 365. This ensures that you are well‑equipped to deal with life’s many challenges.

• Healthcare Cash plan (covers the cost of dental, prescriptions, therapies)
• Headspace App (positive mental wellbeing app, up to 5 users per account)
• Discounted Gym Membership
• Cycle to work scheme
• Discount on pet food
• Free fruit on Mondays
• 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

What’s next?

We’ll take care of you from here on. Firstly, thank you for taking the time to express interest in this opportunity and Dechra. If you’re interested, please apply in the first instance.

We take pride in ensuring you have a positive experience with Dechra and the recruitment process. Our team is friendly and approachable. We won’t ghost you… we’ll always provide updates and feedback regardless of дзяцей, even if the update is, “there’s no update”.

What’s the 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, weindice competency‑based, structured answers to our questions, so please feel free to prepare in advance of the interview.

For further information on your application, reach out to [e-mail].