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- Tasks: Lead QC lab activities, ensuring high standards in compliance and documentation.
- Company: Join a leading company in the pharmaceutical industry based in Oxford.
- Benefits: Competitive salary, pension, and comprehensive benefits package.
- Why this job: Make a real impact in quality control and product development.
- Qualifications: Degree in science and strong experience in cGMP QC environments.
- Other info: Dynamic role with opportunities for growth and leadership.
The predicted salary is between 36000 - 60000 £ per year.
Location: Oxford, UK
Department: Quality, Quality Control
Reporting to: Manager, Quality
Type: Full-time, permanent
About the role
We are looking for a Senior Quality Control Specialist to join our Quality Control team based in Oxford. This is a hands-on senior laboratory role with strong quality system ownership. You will lead day-to-day QC activities, act as a subject matter expert for methods, products, and equipment, and drive high standards in cGMP compliance, data integrity, and right-first-time documentation. You will support routine testing (incoming materials and finished products) and contribute to new product development work where required, helping assess physical and chemical properties and their impact on final products.
Key responsibilities
- QC operations and delivery
- Lead the running of QC laboratory activities, plan workloads, balance priorities, and ensure on-time testing and documentation.
- Generate high-quality results and documents within agreed timelines, using approved procedures and validated systems.
- Technical leadership and compliance
- Act as SME for assigned methods, products, and equipment; provide guidance on execution, troubleshooting, and suitability.
- Ensure activities comply with cGMP, data integrity principles, Summit procedures, and VMD ManSA requirements.
- Approve or author controlled documents within delegated authority, including SOPs, test methods, specifications, logbooks, CoAs, and quality reports.
- Quality system ownership, end-to-end
- Lead deviations and incidents; perform root cause analysis, risk assessments, CAPA definition and implementation, effectiveness checks, and on-time closure.
- Lead OOS, OOT, and laboratory investigation work; coordinate testing and ensure compliant conclusions and narratives.
- Own CAPA and change controls related to methods, equipment, materials, and processes; complete impact assessments, coordinate validation and training, implement and close changes.
- Training, coaching, and leadership
- Lead onboarding and ongoing training for QC personnel, build training matrices, assess competence, and coach analysts in technique and documentation.
- Deliver refresher training on cGMP, data integrity, and investigation quality, tailored to trends and audit findings.
- Validation, equipment, and audits
- Support or lead method verification and validation work, including protocol review, execution, data review, and reporting.
- Oversee equipment qualification and maintenance activities (IQ, OQ, PQ), calibration, PM, and out-of-service controls where required.
- Host and support internal, external, and regulatory audits/inspections; present data clearly and own responses and follow-ups.
What we're looking for
Essential
- Degree (or equivalent) in a science discipline.
- Strong experience in a cGMP QC laboratory environment, with the ability to work independently and make sound decisions with minimal supervision.
- Excellent knowledge of Good Manufacturing Practice and Good Documentation Practice, with a clear commitment to data integrity.
- Proven capability leading investigations (deviations, OOS/OOT) and delivering effective CAPAs and risk assessments.
- Strong communication skills; clear, timely written and verbal communication appropriate to the audience.
- Strong planning and organisation, able to prioritise shifting workloads and deliver to deadlines.
Desirable
- Working knowledge of Waters Empower (HPLC), plus broader chromatography experience.
- Experience supporting method validation/verification and equipment qualification activities.
- Audit hosting experience, and confidence presenting QC data and investigation narratives.
What we offer
Competitive salary, dependent on experience. Competitive contributory pension and a comprehensive benefits package. A varied role with real ownership, impact, and development opportunities within Quality and across the business.
How to apply
If you are interested in this role, please send an updated CV and a short note highlighting your relevant QC experience.
Senior Quality Specialist (Senior QC) in Oxford employer: Summit Veterinary Pharmaceuticals Ltd
Contact Detail:
Summit Veterinary Pharmaceuticals Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Specialist (Senior QC) in Oxford
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it's not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their quality control processes and be ready to discuss how your experience aligns with their needs. We want you to shine and show them why you're the perfect fit!
✨Tip Number 3
Practice common interview questions, especially those related to cGMP compliance and quality systems. We recommend doing mock interviews with friends or mentors to build your confidence and refine your answers.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Senior Quality Specialist (Senior QC) in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Quality Control Specialist role. Highlight your relevant experience in cGMP QC environments and any specific skills that match the job description. We want to see how you fit into our team!
Craft a Compelling Cover Note: Your cover note should be a brief but impactful summary of your QC experience. Use it to showcase your passion for quality control and how your background aligns with our needs. Remember, this is your chance to make a great first impression!
Showcase Your Achievements: When detailing your experience, focus on specific achievements and contributions you've made in previous roles. Whether it's leading investigations or improving compliance, we love to see quantifiable results that demonstrate your impact.
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, it shows you're keen on joining our team at StudySmarter!
How to prepare for a job interview at Summit Veterinary Pharmaceuticals Ltd
✨Know Your Quality Control Basics
Make sure you brush up on your knowledge of cGMP and Good Documentation Practices. Be ready to discuss how you've applied these principles in your previous roles, especially in a QC laboratory environment.
✨Showcase Your Problem-Solving Skills
Prepare examples of past investigations you've led, particularly around deviations or OOS/OOT situations. Highlight your approach to root cause analysis and how you implemented effective CAPAs.
✨Demonstrate Leadership and Training Experience
Think about times when you've trained or coached others in QC processes. Be ready to share how you assess competence and deliver refresher training, especially in relation to cGMP and data integrity.
✨Be Ready for Technical Questions
Expect questions about specific methods and equipment, particularly if you have experience with Waters Empower or chromatography. Prepare to discuss your involvement in method validation and equipment qualification activities.
