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- Tasks: Ensure quality compliance and manage audits in a dynamic pharmaceutical environment.
- Company: Join Britannia Pharmaceuticals, a leader in innovative neurology treatments.
- Benefits: Competitive salary, annual bonus, pension scheme, and generous leave.
- Why this job: Make a real impact on health by ensuring high-quality pharmaceuticals reach those in need.
- Qualifications: Degree in chemistry or life sciences with significant QA experience.
- Other info: Collaborative culture focused on professional development and improving lives.
The predicted salary is between 36000 - 60000 £ per year.
At STADA we pursue our purpose “Caring for people‘s health as a trusted partner” worldwide. Originally founded by pharmacists, we are a leading manufacturer of high-quality pharmaceuticals. More than 12,300 employees around the globe live our values Integrity, Entrepreneurship, Agility and One STADA to achieve ambitious goals and shape the successful future of STADA.
Britannia Pharmaceuticals, part of the STADA Arzneimittel AG group of companies, is a UK based pharmaceutical company specialising in the neurology market. Britannia focuses on innovative products for chronic and serious medical conditions, and in particular, the treatment of Parkinson’s disease. We are highly committed to improving the quality of life for people with Parkinson's disease.
We are looking for a Senior Quality Assurance Officer!
How You Will Make An Impact:
- Support the GxP Quality Management System by conducting audits, managing deviations, and ensuring compliance with EU GMP and GDP standards.
- Manage supplier assurance processes, including external audits, technical agreements, and quality improvement plans.
- Oversee product release to the market, ensuring regulatory compliance and reviewing batch release documentation.
- Act as a Responsible Person (RP) and Responsible Person for Import (RPi), ensuring GDP compliance and addressing non-conformities.
- Conduct risk assessments, implement corrective and preventive actions (CAPA), and deliver training on GDP and regulatory compliance.
- Collaborate with supply chain, logistics, and warehousing teams to ensure efficiency and compliance without compromising product quality.
- Maintain accurate records, respond to regulatory inspections, and ensure continuous professional development (CPD).
What We Are Looking For:
- A degree in chemistry or a related life sciences field, with membership in a professional body (e.g., Royal Society of Chemistry/Biology/Pharmacy).
- Significant QA experience in an EU GMP and GDP-regulated environment, with knowledge of quality management systems and sterile product manufacturing.
- Proven experience as a Responsible Person (RP) or RPi on a named license, with expertise in GDP and GMP auditing.
- Strong decision-making, problem-solving, and risk management skills to address significant non-compliances.
- High attention to detail, excellent communication skills, and the ability to work effectively in a fast-paced regulatory environment.
- Solid understanding of EU regulations and guidance related to GMP and GDP, with experience advising on CAPA, deviations, and change controls.
How We Care For You:
At Britannia, our purpose “Caring for people’s health as a trusted partner” motivates us every day. And what would be a better place than starting with our own colleagues. Which is why we give so much in return:
- Competitive salary and annual bonus scheme.
- Salary Sacrifice Pension Scheme.
- 25 days of annual leave plus.
Senior QA Officer in Reading employer: STADA Arzneimittel AG
Contact Detail:
STADA Arzneimittel AG Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QA Officer in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work at STADA or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU GMP and GDP standards. We want to see you shine, so practice answering questions related to quality assurance and compliance to show you're the perfect fit for the Senior QA Officer role.
✨Tip Number 3
Don’t forget to showcase your problem-solving skills! Think of examples from your past experience where you tackled significant non-compliances or implemented CAPA. This will help us see how you can make an impact at STADA.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re genuinely interested in joining our team and contributing to our mission of caring for people’s health.
We think you need these skills to ace Senior QA Officer in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior QA Officer role. Highlight your relevant experience in QA, especially in EU GMP and GDP environments. We want to see how your skills align with our mission at STADA!
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 you can contribute to our purpose of caring for people's health. Keep it concise but impactful!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've improved processes or ensured compliance in previous roles. We love seeing results that speak for themselves.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at STADA Arzneimittel AG
✨Know Your Stuff
Make sure you brush up on your knowledge of EU GMP and GDP regulations. Familiarise yourself with the latest updates in quality management systems and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Experience
Prepare specific examples from your past work that highlight your experience as a Responsible Person (RP) or RPi. Be ready to explain how you managed audits, handled deviations, and ensured compliance in a fast-paced environment.
✨Demonstrate Problem-Solving Skills
Think of scenarios where you faced significant non-compliances and how you addressed them. Discuss your approach to risk assessments and CAPA implementation, showcasing your decision-making process.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's quality assurance processes and how they align with their mission of caring for people's health. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
