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- Tasks: Manage and develop the stability programme for veterinary medicines, ensuring compliance and quality.
- Company: Join Dechra, a global leader in veterinary pharmaceuticals with a supportive culture.
- Benefits: Enjoy a 9-day fortnight, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on product quality and contribute to a culture of scientific excellence.
- Qualifications: Degree in chemistry or related science; experience in the pharmaceutical industry is a plus.
- Other info: Collaborative team environment with a focus on continuous improvement and personal development.
The predicted salary is between 30000 - 40000 £ per year.
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.
We’re looking for a motivated and detail-driven Stability Specialist to take ownership of our GMP-compliant stability programme for veterinary medicines. This is a fantastic opportunity to play a key role in supporting product quality, regulatory compliance, and operational excellence - all within a friendly, collaborative, and forward-thinking QC department.
The Role
As our Stability Specialist, you’ll maintain and develop the site’s stability programme in line with VICH, FDA, and product licence requirements. You’ll be the go-to person for designing, coordinating, trending, and reporting stability data - ensuring our processes meet the highest standards of cGMP, cGLP, and Health & Safety. This is a non-laboratory testing role; instead, you’ll focus on planning, oversight, data integrity, and cross-department coordination. You’ll help shape best practices, support continuous improvement, and contribute to a culture of quality and scientific excellence.
Key Responsibilities
- Manage the full stability programme, from creating the annual stability plan and report to monitoring packing schedules and initiating stability requests.
- Prepare all supporting documentation, including protocols, templates, and labels, while ensuring samples are set down and tested on time.
- Oversee every timepoint, coordinating sample pulls, issuing work to the QC laboratories, arranging external testing when needed, and maintaining accurate records.
- Analyse stability trends, investigate atypical results, and keep the stability master data up to date.
- Look after the stability chambers by topping up water, monitoring telemetry data, reviewing any deviations, and ensuring the chambers remain well organised with accurate inventories.
- Capacity planning and timely disposal of completed study samples.
- Collate and present KPIs for internal meetings, support regulatory submissions with high-quality data, and contribute to product quality summaries.
- Review documentation prepared by colleagues, maintain and update SOPs, and play an active role in investigations, deviations, CAPAs, and change controls.
- Drive continuous improvement, highlight opportunities for efficiency, and support others’ development through coaching and mentoring.
- Contribute to departmental training and ensure your own knowledge of guidelines and regulations remains current.
Desirable
- Pharmaceutical industry experience
- Basic understanding of formulations and manufacturing processes
- Experience executing stability studies end-to-end
Qualifications
- Degree (or higher) in chemistry or a related applied science
Why You’ll Love Working with Us
You’ll be joining a supportive, collaborative team where your ideas are valued, and your work genuinely makes a difference. Every day brings something new, and you’ll have the chance to grow your skills, build strong relationships, and contribute to a site that prides itself on quality, safety, and continuous improvement.
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 are friendly and approachable. We won’t ghost you..we’ll always provide updates and feedback regardless of the outcome, 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 understand more about 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. In addition to this, we always look for competency-based structured answers to our questions, so feel free to prepare ahead of the interview.
QC Stability Specialist in Skipton employer: Dechra Pharmaceuticals Limited
Contact Detail:
Dechra Pharmaceuticals Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Stability Specialist in Skipton
✨Tip Number 1
Get to know the company culture! Before your interview, dive into Dechra's values and mission. This will help you connect your own experiences with what they stand for, showing that you're not just a fit for the role, but for the team too.
✨Tip Number 2
Practice makes perfect! Prepare for those competency-based questions by thinking of specific examples from your past work. Use the STAR method (Situation, Task, Action, Result) to structure your answers and keep them clear and concise.
✨Tip Number 3
Don’t forget to ask questions! At the end of your interview, have a few thoughtful questions ready about the role or the team. This shows your genuine interest and helps you figure out if Dechra is the right place for you.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, it gives you a chance to explore more about the company and the roles we offer. Let’s get you on board!
We think you need these skills to ace QC Stability Specialist in Skipton
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the QC Stability Specialist role. Highlight your relevant experience in stability programmes and GMP compliance, showing us why you're the perfect fit for our team.
Showcase Your Skills: Don’t just list your qualifications; demonstrate how your skills align with our values of Dedication, Enjoyment, Courage, Honesty, Relationships, and Ambition. We want to see how you embody these traits in your work!
Be Clear and Concise: When writing your application, keep it straightforward and to the point. Use clear language and avoid jargon where possible. We appreciate a well-structured application that’s easy to read and understand.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role there!
How to prepare for a job interview at Dechra Pharmaceuticals Limited
✨Know Your Stuff
Make sure you brush up on your knowledge of GMP, cGMP, and stability studies. Familiarise yourself with VICH and FDA guidelines as they relate to veterinary pharmaceuticals. This will show that you're not just interested in the role but also understand the industry standards.
✨Show Your Passion for Quality
Dechra values quality and continuous improvement, so be ready to discuss how you've contributed to these areas in your previous roles. Share specific examples of how you've driven improvements or maintained high standards in your work.
✨Prepare for Competency Questions
Since the interview style is conversational yet structured, prepare for competency-based questions. Think of situations where you've demonstrated skills like problem-solving, teamwork, and attention to detail. Use the STAR method (Situation, Task, Action, Result) to frame your answers.
✨Ask Thoughtful Questions
At the end of the interview, don’t forget to ask insightful questions about the team, the stability programme, or Dechra's future plans. This shows your genuine interest in the role and helps you determine if it's the right fit for you.