Job Introduction
QC Project Analyst, 9 Month FTC
Site Based - Skipton, UK
0800-1630 hrs, Mon-Fri over a nine-day fortnight (every second Friday off)
This is a fixed-term contract for a minimum of 9 months initially.
About The Role
We are embarking on a key programme to enhance our product portfolio, and we are looking for a QC Project Analyst to help shape how this work is delivered. The purpose of this role is to support new product integration and execute process validation. This is a role for someone who enjoys improving systems, refining methods, and contributing to meaningful change within a pharmaceutical QC environment.
You will be part of a team committed to excellence, working closely with colleagues across Quality Control, MS&T, Regulatory Affairs, and other Dechra sites to ensure our analytical methods are robust, compliant, and ready for future validation activities.
A Little About Us
Dechra is a growing global specialist in 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.
What You’ll Be Doing
Your day‑to‑day work will focus on validating analytical methods—particularly those involving HPLC, UPLC, and dissolution testing. The core activities will be to prioritise redevelopment methods across several analytical techniques, primarily HPLC/UPLC and Dissolution. You’ll be responsible for raw material verification and designing and executing method development protocols, then taking those methods through validation or verification to ensure they meet regulatory and scientific expectations.
This role also involves managing change controls, supporting licence updates, and collaborating with at least one other Dechra site to ensure smooth method transfer. You’ll be hands‑on in the laboratory, maintaining high standards of cGMP, cGLP, and Health & Safety, while keeping meticulous records and contributing to investigations when issues arise. It’s a position that blends technical expertise with structured project work, offering variety and the chance to influence how our QC function evolves.
How Success Will Be Measured
We value accuracy, efficiency, and a proactive mindset. You’ll be expected to deliver analysis “Right First Time,” meet agreed throughput timelines, and take ownership of investigations and continuous improvement activities. The role emphasises the importance of fulfilling responsibilities and demonstrating behaviours aligned with Dechra’s values, ensuring your contribution supports both personal and departmental objectives.
What You Bring
We’re looking for someone who combines technical capability with strong communication and organisational skills. You should feel comfortable working independently but also enjoy collaborating with colleagues. The role calls for someone who can plan effectively, solve problems with confidence, and present data clearly and meaningfully. As the document notes, you’ll need the ability to accurately and meaningfully gather, assess and report on data… excellent technical writing skills… knowledge in transfer, validation and verification processes within the pharmaceutical industry. Your technical writing skills will play a key role when collaborating with various other functions.
Experience with chemical and physical analytical techniques, alongside a solid understanding of GMP regulations across the UK, EU, and US, will help you thrive. Attention to detail—whether in data, documentation, or formatting—is essential.
Qualifications
You’ll hold an HNC/D, BSc, or equivalent in a science discipline, or have relevant job‑specific experience that demonstrates your capability. An analytical chemistry degree will give you the foundations for success.
Why You’ll Love It Here
This is a career with real purpose — one you can genuinely feel proud of. We work a 9-day fortnight at our Skipton site, which means every second Friday is yours to enjoy. Longer weekends, more time with family and friends, and a healthier work-life balance.
We also care deeply about the well-being of our people. You’ll have full access to our Employee Assistance Programme, offering confidential emotional, physical, and financial support 24/7, 365 days a year. On top of that, you’ll also have access to the following:
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Healthcare cash plan
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Headspace wellbeing app
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Discounted gym membership
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Cycle to work scheme
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Pet food discounts
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Free fruit on Mondays
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Free onsite parking (including electric charging)
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22.5 days’ annual leave plus bank holidays, and the option to buy an extra week of holiday each year
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8% employer pension contribution
What Happens Next
Thank you for taking the time to explore this opportunity with us. If it sounds like the right fit, we’d love you to apply. We’re committed to giving every candidate a positive experience — we won’t leave you wondering what’s happening. You’ll always receive updates and feedback, and if you ever feel out of the loop, just give us a nudge.
The Interview Process
You’ll usually start with a friendly phone call from our recruitment team so we can get to know you a little better. Most roles involve a two-stage interview — one via MS Teams and one face-to-face. We may also ask you to complete a short personality questionnaire beforehand. Our interview style is relaxed and conversational, though we do use competency-based questions, so preparing a few examples in advance is always helpful.
If you’d like more information about your application, you can reach us at [email protected]
