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- Tasks: Ensure high-quality medicines meet strict standards in a fast-paced environment.
- Company: Curium, the world's largest nuclear medicine company with over a century of experience.
- Benefits: Competitive salary, supportive team culture, and opportunities for professional growth.
- Why this job: Make a real difference in patient care while working with cutting-edge radiopharmaceuticals.
- Qualifications: Science degree and 2-3 years in QA/QC or GMP pharmaceutical settings.
- Other info: Join a diverse team committed to innovation and excellence in healthcare.
The predicted salary is between 36000 - 60000 £ 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 Radiopharmacy team at UCLH and support the delivery of high-quality medicines in a highly regulated hospital environment. This is a hands‑on role ideal for quality professionals who thrive in fast‑paced, precision‑driven settings.
What You’ll Do:- You will play a key role in maintaining GMP compliance across the Quality Management System and QC laboratory by:
- Ensuring production, analytical methods, and documentation comply with GMP, Specials guidance, and pharmacopeia standards (EP/BP/SmPC)
- Supporting core QMS processes including Deviations, OOS, CAPA, Change Control, Complaints, Recalls, and Risk Assessments
- Performing and reviewing QC and microbiology testing, including environmental monitoring and sterility data review
- Supporting batch release activities and acting as Releasing Officer under delegation
- Leading and supporting Root Cause Analysis and CAPA identification
- Maintaining inspection readiness and supporting regulatory and customer audits
- Managing validation activities, protocols, and ensuring the Validation Master Plan remains current
- Maintaining QC equipment calibration, maintenance schedules, and laboratory stock levels
- Driving data integrity, logbook management, and archiving of QC and batch documentation
- Supporting training compliance for personnel performing QC activities
- Coordinating and supporting internal self‑inspections
Qualifications:
- Science degree (Pharmacy, Chemistry, Biology, or related)
- 2–3 years’ experience in Radiopharmacy QA/QC or GMP pharmaceutical environment
- Strong working knowledge of GMP and pharmaceutical quality systems
- Excellent attention to detail and strong practical laboratory capability
- Strong teamwork, communication, and stakeholder collaboration skills
- Ability to work under pressure in a clinical manufacturing environment
- Strong organisation and time management skills
- Radiation knowledge (desirable)
- Willingness to work shifts
QA/QC Specialist employer: Curium Pharma
Contact Detail:
Curium Pharma Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA/QC Specialist
✨Tip Number 1
Network like a pro! Reach out to folks in the QA/QC field, especially those at Curium or similar companies. A friendly chat can open doors and give you insider info on what they’re really looking for.
✨Tip Number 2
Prepare for the interview by brushing up on GMP compliance and quality systems. We want you to show off your knowledge and experience, so think of examples from your past roles that highlight your skills in a fast-paced environment.
✨Tip Number 3
Don’t forget to showcase your teamwork skills! Curium values collaboration, so be ready to discuss how you’ve worked with others to solve problems or improve processes in your previous jobs.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our team at Curium. Let’s get you started on this exciting journey!
We think you need these skills to ace QA/QC Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA/QC Specialist role. Highlight your experience in GMP compliance and any relevant laboratory skills. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in radiopharmacy and how you can contribute to our team. Keep it concise but impactful!
Showcase Your Attention to Detail: In QA/QC, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their application is polished and professional.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the info you need about the role and our company!
How to prepare for a job interview at Curium Pharma
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) regulations before the interview. Curium is looking for someone who can ensure compliance, so being able to discuss specific GMP standards and how they apply to radiopharmacy will show that you're serious about the role.
✨Showcase Your Lab Skills
Since this role involves hands-on laboratory work, be prepared to talk about your practical experience in a lab setting. Highlight any specific QC or microbiology testing you've performed, and be ready to discuss how you maintain attention to detail in high-pressure situations.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills, especially around deviations, CAPA, and risk assessments. Think of examples from your past experience where you successfully identified and resolved issues, as this will demonstrate your ability to thrive in a fast-paced environment.
✨Emphasise Teamwork and Communication
Curium values strong collaboration, so be ready to share examples of how you've worked effectively within a team. Discuss how you communicate with stakeholders and support training compliance, as these skills are crucial for maintaining quality standards in a clinical setting.