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- Tasks: Lead sterility assurance projects and ensure compliance with industry standards.
- Company: Join a global leader in pharmaceuticals with a focus on innovation.
- Benefits: Competitive salary, professional development opportunities, and relocation package available.
- Why this job: Make a real impact in drug development and contamination control.
- Qualifications: Degree in Science or Engineering and strong project management skills.
- Other info: Champion a culture of continuous improvement in a dynamic work environment.
The predicted salary is between 72000 - 84000 £ per year.
This is an excellent opportunity to join a global pharmaceuticals organisation in a new Quality Assurance Expert lead appointment. You will be responsible for Sterility Assurance across the GMP site, projects, new drug development areas and have overall sterile responsibility, ensuring compliance with regulatory requirements and global industry standards.
Key Experience- Annex 1 GMP - manufacturing of sterile medicinal products
- Lead sterility quality assurance expert
- GMP Pharmaceuticals
- Drive contamination control strategies
- Provide strategic oversight
- Process improvements / quality / risk management
- Pharmaceuticals / life sciences Quality Assurance
- Lead sterility assurance projects to ensure contamination control strategies are effectively implemented and aligned with site objectives and regulatory requirements.
- Provide overall oversight of facility operations, ensuring compliance with sterility assurance standards and contamination control measures.
- Drive the implementation of sterility assurance programmes across facilities, collaborating with cross-functional teams site and above site teams to ensure consistency and effectiveness.
- Collaborate with operations and quality teams to ensure contamination control measures are integrated effectively into manufacturing processes.
- Monitor performance metrics related to facility operations and contamination control, identifying areas for improvement and implementing corrective actions as needed.
- Sharing knowledge and best practices globally.
- Develop and deliver training programs, ensuring staff understand and consistently apply sterility assurance and contamination control measures.
- Support the strategic planning and execution of facility upgrades or projects to optimise contamination control systems and ensure regulatory compliance.
- Sponsorship of Investigations and Root Cause Analysis: Sponsor investigations and root cause analysis for deviations, providing strategic leadership and overseeing corrective and preventive actions.
- Culture Leadership: Champion a culture of continuous improvement, innovation, and excellence, promoting a positive and inclusive work environment.
- Degree in Science, Engineering or related field.
- Bachelor's degree in Chemistry, Biochemistry, Microbiology, or a related field.
- Advanced certifications.
- Proficiency in sustainability software and data analysis tools.
- Strong communication, project management, and client engagement skills.
- Leading salary and benefits package.
- Opportunities for professional development and extra certifications.
Quality Assurance Manager - Pharmaceuticals / Life Sciences employer: Found Consultancy
Contact Detail:
Found Consultancy Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Manager - Pharmaceuticals / Life Sciences
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceuticals and life sciences sectors on LinkedIn. Join relevant groups, attend webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by researching the company inside out. Understand their products, values, and recent news. We want you to walk in with confidence, ready to discuss how your experience aligns with their goals, especially around sterility assurance and contamination control.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors. Focus on articulating your experience in GMP and quality assurance clearly. We’re here to help you shine, so don’t hesitate to ask for feedback on your responses.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive opportunities listed there. So, keep an eye out and make sure you’re one of the first to apply!
We think you need these skills to ace Quality Assurance Manager - Pharmaceuticals / Life Sciences
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Manager role. Highlight your experience with GMP, sterile medicinal products, and any relevant projects you've led. We want to see how your background aligns with our needs!
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 pharmaceuticals and how you can contribute to our team. Keep it engaging and relevant to the job description.
Showcase Your Achievements: Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've driven contamination control strategies or improved processes in previous roles. We love seeing results!
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 Found Consultancy
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and how they apply to sterile medicinal products. Be ready to discuss specific examples from your past experience where you've successfully implemented these practices.
✨Showcase Your Leadership Skills
As a Quality Assurance Manager, you'll need to lead sterility assurance projects. Prepare to share instances where you've led teams or initiatives, focusing on how you drove contamination control strategies and improved processes.
✨Be Ready for Technical Questions
Expect questions about contamination control measures and sterility assurance programmes. Brush up on the latest industry standards and be prepared to discuss how you've integrated these into manufacturing processes in your previous roles.
✨Demonstrate Your Continuous Improvement Mindset
This role requires a champion for continuous improvement. Think of examples where you've identified areas for improvement and implemented corrective actions. Highlight your ability to foster a culture of innovation and excellence within your team.