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Quality Control Stability Specialist
2 months ago
Role Summary
We appreciate your interest in exploring this opportunity with Dechra. As a key player in the veterinary pharmaceutical sector, we are excited to share more about the QC Stability Specialist position.
Quality Control Stability Specialist
Site-based, Skipton
Full-time, Permanent
Days, 36 hrs, Mon - Fri with every other Friday off
Dechra is a rapidly expanding global leader in veterinary pharmaceuticals, dedicated to the development, production, marketing, and distribution of premium products exclusively for veterinary professionals worldwide. This is an opportune moment to join our modern facility in Skipton, which is undergoing significant enhancements as we embrace a transformative phase of growth.
Employee Benefits
Our QC team in Skipton fosters a supportive work environment that encourages collaboration and shared success. You will benefit from a wealth of expertise within the department, including specialists in Quality, Technical, and Analytical fields. Your contributions will be valued, and you will have ample opportunities for professional growth.
We offer a competitive compensation package that includes:
- Average 36-hour work week (with a day off every other Friday)
- 22.5 days of annual leave plus public holidays
- Option to purchase an additional week of holiday each year
- 8% Employer Pension Contribution
- Complimentary access to the Headspace App
- Employee Assistance Programme
- On-site parking facilities
- Volunteering opportunities
- Company-sponsored events
Key Responsibilities
In this role, you will oversee and coordinate the GMP-compliant stability program for veterinary medicines at Dechra Skipton, ensuring adherence to VICH and product license standards, with guidance from the Stability Specialist.
Your responsibilities will include:
- Providing technical and administrative support for the design, execution, trending, and reporting of stability data.
- Coordinating both in-house and external stability testing capabilities and control measures.
- Managing the stability management program, including:
- Processing new sample requests (routine and ad-hoc)
- Overseeing the lifecycle management of samples, from setup to destruction
- Managing pull dates and sample retrieval
Additional duties may involve:
- Submitting samples to external testing facilities
- Conducting trend analysis and reporting OOS/T results
- Authoring Stability Protocols and Reports
- Monitoring stability cabinet/chamber telemetry
- Compiling and reporting KPIs and quality metrics
- Writing, reviewing, and updating SOPs as necessary
- Participating in Laboratory Investigation Reports (LIRs) and managing deviations, change controls, CAPAs, and effectiveness reviews
- Contributing to departmental development by identifying inefficiencies
- Supporting management in executing their responsibilities
- Upholding and promoting the company's core values in all interactions
- Performing other duties as assigned
Ideal Candidate Profile
To excel in this position, you should possess a background in analysis, which will aid in data interpretation. Strong communication skills are essential for collaboration with various departments, while the ability to work independently is crucial for daily tasks.
Key qualifications include:
- Attention to detail and precision
- Coaching and mentoring abilities
- Effective communication tailored to the audience
- Problem-solving skills
- Pragmatic approach
- Minimum of 2 years of relevant experience in a Quality Control/Assurance or R&D environment within a GMP-compliant setting
- Understanding of VICH guidelines and experience with stability programs
- Familiarity with GMP regulations applicable to products in the UK, EU, Japan, and US
- Knowledge of environmental, health & safety, and regulatory standards
- Proficiency in Microsoft Office applications (Word, Excel) with a focus on detail and clarity
- Minimum educational requirement of HND in a relevant scientific discipline or equivalent experience
Whether you are an established QC professional or have a couple of years of industry experience seeking your next career advancement, our diverse and experienced team looks forward to welcoming you.
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