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- Tasks: Ensure quality compliance and manage audits in a dynamic pharmaceutical environment.
- Company: Join Britannia Pharmaceuticals, part of the global STADA family, dedicated to improving health.
- Benefits: Enjoy competitive salary, annual bonuses, health benefits, and generous leave options.
- Why this job: Make a real impact on patients' lives while advancing your career in quality assurance.
- Qualifications: Degree in chemistry or life sciences with significant QA experience in regulated environments.
- Other info: Be part of a supportive team that values integrity, agility, and professional growth.
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.
Brittania 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).
- 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.
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 bank holidays with the potential to buy up to 5 additional days.
- Health benefits provided through BUPA Private Medical Insurance.
- Free winter flu jab.
- Wellbeing support through our Employee Assistance Programme and KYAN Wellbeing – offering free coaching and counselling services for you and your family.
- Electric Car Scheme through Octopus Energy.
- Cycle to Work Scheme.
- Enhanced Family Leave.
- Plus, many more colleague benefits & celebration events.
Are you looking for new challenges where you can make a difference for people’s health? We are looking for candidates with positive attitude, expert knowledge and an entrepreneurial spirit that enjoy friendly working environment in a global team. We would be pleased to get to know you.
Please use our online job portal to submit your application: https://jobs.stada.com
Senior QA Officer in Reading employer: STADA Group
Contact Detail:
STADA Group 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 current or former employees at STADA on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of EU GMP and GDP standards. We want to see that you’re not just familiar with the terms but can also discuss how they apply in real-world scenarios.
✨Tip Number 3
Show off your problem-solving skills! Think of examples from your past experience where you tackled significant non-compliances or implemented CAPA. We love candidates who can think on their feet.
✨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 STADA.
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 engaging and personal!
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Whether it’s successful audits or implementing CAPA, we love to see how you’ve made an impact in your previous roles.
Apply Through Our Website: We encourage you to apply through our online job portal. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at STADA Group
✨Know Your Stuff
Make sure you brush up on your knowledge of EU GMP and GDP regulations. Familiarise yourself with the specific quality management systems and sterile product manufacturing processes that are relevant to the role. This will not only help you answer questions confidently but also show your genuine interest in the position.
✨Showcase Your Experience
Prepare to discuss your previous QA experience, especially any roles where you acted as a Responsible Person (RP) or RPi. Be ready to share specific examples of how you've managed deviations, conducted audits, or implemented CAPA. This will demonstrate your hands-on expertise and problem-solving skills.
✨Ask Insightful Questions
Interviews are a two-way street! Prepare thoughtful questions about the company's approach to quality assurance, their current challenges, or how they support continuous professional development. This shows that you're not just interested in the job, but also in how you can contribute to their mission.
✨Emphasise Team Collaboration
Since the role involves working closely with supply chain, logistics, and warehousing teams, be prepared to discuss your experience in collaborative environments. Highlight instances where you’ve successfully worked with cross-functional teams to ensure compliance without compromising product quality.
