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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 collaborative culture.
- Benefits: Enjoy a 9-day fortnight, competitive salary, and opportunities for professional growth.
- Other info: Be part of an exciting period of change and growth at our modern Skipton facility.
- Why this job: Make a real impact on product quality and regulatory compliance in a friendly team.
- Qualifications: Degree in chemistry or related science; experience in stability studies is a plus.
The predicted salary is between 30000 - 40000 £ per year.
Vacancies for a QC Stability Specialist on a Day Shift from 08:00 to 16:30 hrs, with a 9-day fortnight and every second Friday off in Skipton, site-based.
Dechra is a growing, global specialist within the world of veterinary pharmaceuticals, focusing on the development, manufacture, marketing, and sales of high-quality products exclusively for veterinarians worldwide. Our modern Skipton facility is undergoing exciting changes due to further investment.
We are looking for a motivated and detail-driven Stability Specialist to take ownership of our GMP-compliant stability programme for veterinary medicines. This role is key in supporting product quality, regulatory compliance, and operational excellence within a friendly, collaborative, and forward-thinking QC department.
The RoleAs our Stability Specialist, you will maintain and develop the site’s stability programme in line with VICH, FDA, and product licence requirements. You will design, coordinate, trend, and report stability data, ensuring our processes meet the highest standards of cGMP, cGLP, and Health. Your focus will be on planning, oversight, data integrity, and cross-department coordination, helping to shape best practices and support continuous improvement.
Key Responsibilities- Manage the full stability programme, including creating the annual stability plan and report.
- Monitor packing schedules and initiate stability requests.
- Prepare supporting documentation, including protocols, templates, and labels.
- Ensure samples are set down and tested on time.
- Oversee every timepoint throughout each study, coordinating sample pulls and issuing work to the QC laboratories.
- Arrange external testing when needed and maintain accurate records.
- Analyse stability trends and investigate atypical results.
- Keep the stability master data up to date.
- Look after the stability chambers, monitoring telemetry data and ensuring they remain well organised.
- Plan capacity and dispose of completed study samples in a timely manner.
- Collate and present KPIs for internal meetings and support regulatory submissions with high-quality data.
- Review documentation prepared by colleagues and maintain/update SOPs.
- Participate in investigations, deviations, CAPAs, and change controls.
- Drive continuous improvement and highlight opportunities for efficiency.
- Support others’ development through coaching and mentoring.
- Contribute to departmental training and ensure your knowledge of guidelines and regulations remains current.
- Pharmaceutical industry experience.
- Basic understanding of formulations and manufacturing processes.
- Experience executing stability studies end-to-end.
- Degree (or higher) in chemistry or a related applied science.
QC Stability Specialist employer: Dechra Pharmaceuticals Plc
Contact Detail:
Dechra Pharmaceuticals Plc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Stability Specialist
✨Tip Number 1
Network like a pro! Reach out to current employees at Dechra on LinkedIn or through industry events. A friendly chat can give us insights into the company culture and maybe even a referral!
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of GMP and stability studies. We want to show that we’re not just passionate but also knowledgeable about the role and its responsibilities.
✨Tip Number 3
Practice common interview questions, especially those related to quality control and data integrity. We can even do mock interviews with friends to build confidence and refine our answers.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows that we’re genuinely interested in being part of the Dechra family.
We think you need these skills to ace QC Stability Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QC Stability Specialist role. Highlight your relevant experience in managing stability programmes and any specific knowledge of GMP and regulatory compliance. We want to see how your background aligns with our values and the responsibilities outlined in the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for veterinary pharmaceuticals and how you can contribute to our team. Be sure to mention specific examples of your past work that demonstrate your attention to detail and commitment to quality, as these are key for us at Dechra.
Showcase Your Communication Skills: As communication is vital in this role, make sure to highlight your ability to present data clearly and effectively. Whether it's in your CV or cover letter, we want to see how you've successfully communicated complex information in previous roles, especially in a collaborative environment.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of success. This way, your application goes straight to us, and we can review it promptly. Plus, it shows you're keen on joining our Dechra family!
How to prepare for a job interview at Dechra Pharmaceuticals Plc
✨Know Your GMP and Stability Basics
Before the interview, brush up on Good Manufacturing Practices (GMP) and stability study protocols. Being able to discuss these concepts confidently will show that you understand the core responsibilities of a QC Stability Specialist.
✨Showcase Your Attention to Detail
Prepare examples from your past experiences where your attention to detail made a difference. Whether it was in managing data integrity or coordinating sample pulls, specific anecdotes will highlight your suitability for maintaining high standards in stability programmes.
✨Emphasise Team Collaboration
Dechra values relationships and teamwork, so be ready to discuss how you've worked collaboratively in previous roles. Share instances where you contributed to cross-department coordination or supported colleagues, as this aligns with their culture of collaboration.
✨Prepare Questions About Continuous Improvement
Think of insightful questions regarding how Dechra approaches continuous improvement within their QC department. This shows your interest in not just the role but also in contributing to their culture of quality and scientific excellence.