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- Tasks: Ensure life-changing medicines are produced safely and to the highest standards.
- Company: Curium, the world’s largest nuclear medicine company with over a century of experience.
- Benefits: Join a dynamic team in a high-impact role with opportunities for growth.
- Why this job: Make a real difference in healthcare by ensuring quality in radiopharmaceuticals.
- Qualifications: Degree in relevant field and 2 years’ experience in GMP-regulated environments.
- Other info: Collaborative culture focused on respect, dignity, and equality for all.
The predicted salary is between 30000 - 50000 £ per year.
Curium is the world’s largest nuclear medicine company with more than a century of industry experience. We develop, manufacture, and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage, combined with a pioneering approach, is the hallmark of delivering innovation, excellence, and unparalleled service.
Join our Oxford Radiopharmacy team and help ensure life-changing medicines are produced safely, compliantly, and to the highest international standards. This is a hands-on, high-impact role in a highly regulated, technically advanced environment where quality truly matters.
What You’ll Do:- Play a central role in maintaining and improving site quality performance by ensuring production, analytical methods, and documentation comply with GMP, Specials guidance, and international pharmacopoeia standards.
- Manage and improve key Quality System elements, including Deviations, OOS, CAPA, Change Control, Complaints, Risk Assessments, and trending.
- Support batch record review, material release activities, and QP release readiness.
- Maintain inspection readiness and support regulatory inspections and internal self-inspections.
- Oversee validation documentation and ensure equipment and processes meet validation master plan requirements.
- Support QC and microbiology activities, including environmental monitoring, data review, and OOS investigation.
- Drive data integrity, SOP lifecycle management, and continuous QMS improvement.
- Contribute to quality reviews, site quality culture, and cross-functional collaboration.
Qualifications:
- Degree in Pharmacy, Chemistry, Pharmaceutical Chemistry, Biology, or related field.
- Minimum 2 years’ experience working within Quality Systems in a GMP-regulated environment.
- Strong, current knowledge of EU GMP requirements.
- Excellent technical, analytical, and problem-solving skills.
- Strong communication and stakeholder collaboration ability.
- Ability to perform under pressure in a fast-paced manufacturing environment.
- Strategic mindset with focus on continuous improvement.
- Radiation knowledge (desirable, not essential).
Curium is an equal-opportunity employer and believes everyone deserves respect, dignity, and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Senior Quality Assurance Officer in Oxford employer: Curium Pharma
Contact Detail:
Curium Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Assurance Officer in Oxford
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, especially those at Curium. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for the interview by brushing up on your GMP knowledge and quality systems. We want to see how you can apply your skills in real-world scenarios, so think of examples from your past experience that showcase your problem-solving abilities.
✨Tip Number 3
Show your passion for quality assurance! During interviews, let us know why you care about maintaining high standards and how you’ve contributed to quality improvements in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team at Curium.
We think you need these skills to ace Senior Quality Assurance Officer in Oxford
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience that match the Senior QA Officer role. Highlight your knowledge of GMP and any relevant quality systems you've worked with. We want to see how you can contribute to our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how your background aligns with our mission at Curium. Let us know what excites you about this role!
Showcase Your Problem-Solving Skills: In your application, give examples of how you've tackled challenges in a GMP-regulated environment. We love seeing candidates who can think on their feet and drive continuous improvement—so don’t hold back!
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be one step closer to joining our amazing team at Curium!
How to prepare for a job interview at Curium Pharma
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and how they apply to the role. Curium is looking for someone who can demonstrate a strong understanding of EU GMP requirements, so be ready to discuss specific examples from your past experience.
✨Showcase Your Problem-Solving Skills
Prepare to share instances where you've tackled quality issues or improved processes in a regulated environment. Highlight your analytical skills and how you've used them to drive continuous improvement in Quality Systems.
✨Communicate Effectively
Since this role involves collaboration with various stakeholders, practice articulating your thoughts clearly. Be prepared to discuss how you've successfully communicated complex quality concepts to non-technical team members in the past.
✨Be Ready for Technical Questions
Expect some technical questions related to quality assurance and validation processes. Brush up on your knowledge of deviation management, CAPA, and risk assessments, as these are key elements of the role that you’ll need to be familiar with.