At a Glance
- Tasks: Ensure compliance with GMP standards and manage quality control processes in a dynamic environment.
- Company: Leading provider in the innovative nuclear medicine sector.
- Benefits: Competitive salary, bonus potential, and career development opportunities.
- Other info: Join a globally recognised organisation committed to excellence and continuous improvement.
- Why this job: Make a real difference in healthcare while working with cutting-edge radiopharmaceutical processes.
- Qualifications: Degree in a related science field and 2-3 years of relevant experience.
The predicted salary is between 35000 - 45000 £ per year.
We are currently looking for a QA/QC Officer to join a leading provider in the nuclear medicine sector based in our client’s state‑of‑the‑art facility. This exciting opportunity is ideal for professionals with a background in radiopharmacy or laboratory quality control, eager to contribute to innovative healthcare solutions that make a real difference worldwide. As QA/QC Officer, you will be instrumental in ensuring site compliance with GMP standards, international pharmaceutical legislation, and company requirements. This is a key role supporting the quality assurance and quality control functions within a dynamic, fast‑paced environment, with a focus on maintaining high standards of safety, accuracy, and regulatory adherence.
KEY DUTIES AND RESPONSIBILITIES
- Ensure site compliance with GMP, Specials guidelines, and relevant pharmaceutical legislation through review and oversight of production and analytical methods.
- Manage documentation processes including reviewing, updating SOPs, and writing new procedures to uphold quality standards.
- Support investigation activities related to deviations, OOS results, CAPA, change controls, and release of incoming materials.
- Review QC tests and microbiological results, managing out‑of‑specification outcomes, and ensuring timely record updates.
- Perform analytical method validation, execute validation protocols, and support equipment calibration and requalification activities.
ROLE REQUIREMENTS
- A Degree or higher level in a related science field (e.g., Pharmaceutical Chemistry, Quality Assurance, Quality Management).
- Proven 2‑3 years of radiopharmacy or laboratory experience, with knowledge of GMP compliance and QC processes.
- Familiarity with equipment qualification, process validation, and working within a quality department is highly desirable.
WHAT’S IN IT FOR YOU?
Joining our client offers an excellent platform to develop your career within the innovative field of nuclear medicine. You will be part of a globally recognized organization committed to excellence and continuous improvement. The role provides exposure to cutting‑edge radiopharmaceutical processes, working with a dedicated team in a collaborative environment, alongside competitive salary and bonus potential.
QA/QC Officer in London employer: Hyper Recruitment Solutions LTD
As a leading provider in the nuclear medicine sector, our client offers an exceptional work environment that prioritises innovation and excellence. Employees benefit from a collaborative culture, competitive salaries, and opportunities for professional growth within a globally recognised organisation dedicated to advancing healthcare solutions. Joining this dynamic team means contributing to meaningful projects while ensuring compliance with the highest quality standards in a state-of-the-art facility.
Contact Details:
Hyper Recruitment Solutions LTD Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land QA/QC Officer in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the nuclear medicine sector on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that QA/QC Officer role.
✨Tip Number 2
Prepare for interviews by brushing up on GMP standards and quality control processes. We recommend practising common interview questions related to your experience in radiopharmacy and QC. Show them you know your stuff!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your expertise in QA/QC and radiopharmacy.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in their minds.
We think you need these skills to ace QA/QC Officer in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the QA/QC Officer role. Highlight your experience in radiopharmacy or laboratory quality control, and don’t forget to mention any GMP compliance knowledge you have. 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 the nuclear medicine sector and how your skills can contribute to our innovative healthcare solutions. Keep it engaging and relevant to the role.
Showcase Relevant Experience:When detailing your work experience, focus on specific examples that demonstrate your familiarity with QC processes, documentation management, and compliance with pharmaceutical legislation. We love seeing concrete achievements that reflect your capabilities!
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 details you need about the role and our company culture there!
How to prepare for a job interview at Hyper Recruitment Solutions LTD
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) standards before the interview. Be ready to discuss how you've applied these principles in your previous roles, especially in radiopharmacy or laboratory settings.
✨Showcase Your Documentation Skills
Since managing documentation is a key part of the role, prepare examples of how you've reviewed or updated SOPs in the past. Highlight any experience you have with writing new procedures to maintain quality standards.
✨Be Ready for Technical Questions
Expect questions about analytical method validation and equipment calibration. Familiarise yourself with common QC tests and microbiological results, and be prepared to discuss how you've handled out-of-specification outcomes.
✨Demonstrate Your Problem-Solving Skills
Prepare to talk about your experience with investigations related to deviations, OOS results, and CAPA. Think of specific examples where you identified root causes and implemented effective solutions to improve processes.
