At a Glance
- Tasks: Ensure quality and compliance in global medicine operations while driving improvements.
- Company: Join a leading global medicines organisation with a focus on quality.
- Benefits: Competitive salary, career growth, and opportunities for professional development.
- Other info: Dynamic role with opportunities to work globally and improve quality systems.
- Why this job: Be a key player in maintaining high-quality standards across diverse markets.
- Qualifications: Degree in Life Sciences and experience in quality or regulatory environments.
The predicted salary is between 45000 - 60000 £ per year.
We are seeking a talented Quality professional to join a global medicines organisation supporting affiliate-level quality operations across regions. This is an exciting opportunity to work at the intersection of quality, compliance, and business operations, ensuring global standards are effectively implemented at the local level.
You will act as a trusted quality partner, embedding quality systems into business processes, driving compliance, and supporting inspection readiness across diverse markets.
This role is available at Associate, Senior Associate, or Principal level, depending on experience.
What You'll Be Doing- Quality Systems & Compliance
- Support the development and implementation of local and regional quality systems aligned with global standards
- Manage key quality processes including deviations, CAPA, change control, and quality documentation
- Interpret and apply regulatory requirements (GxP) across business activities
- Quality Oversight & Risk Management
- Monitor compliance and proactively identify risks, gaps, and improvement opportunities
- Perform trend analysis and recommend corrective and preventative actions
- Contribute to risk assessments, quality plans, and continuous improvement initiatives
- Audit & Inspection Readiness
- Support and coordinate internal and external audits and inspections
- Ensure teams are inspection-ready with appropriate documentation and processes
- Manage audit responses and ensure timely closure of CAPAs
- Business Partnering
- Act as a quality advisor to cross-functional teams
- Support teams in interpreting regulatory and quality requirements
- Build strong relationships across affiliate and global teams
- Continuous Improvement
- Drive process improvements and simplification initiatives
- Identify opportunities to enhance quality systems and workflows
- Share best practices across regions and global teams
- Essential
- Degree in a Life Sciences or Healthcare-related field (e.g. Pharmacy, Nursing, Biomedicine)
- Experience in quality, clinical development, pharmacovigilance, or regulatory environments
- Strong knowledge of GxP frameworks (GMP, GCP, and/or GVP)
- Experience with: CAPA, deviations, and change control
- Quality systems and compliance processes
- Strong analytical, problem-solving, and communication skills
- Ability to manage multiple priorities in a dynamic, global environment
- Nice to Have
- Experience in affiliate or regional quality roles
- Exposure to audit/inspection management
- Familiarity with risk-based decision-making approaches
- Experience working in global or matrix organisations
If this is something you're interested in, apply or get in touch - jamie.keith@cpl.com
Senior Quality Assurance Specialist in Bracknell employer: Cpl Life Sciences
Join a leading global medicines organisation that prioritises quality and compliance while fostering a collaborative work culture. As a Senior Quality Assurance Specialist, you will benefit from extensive employee growth opportunities, including professional development in a dynamic environment, and the chance to make a meaningful impact on healthcare standards across diverse markets. With a commitment to continuous improvement and strong support for work-life balance, this role offers a unique opportunity to thrive in a purpose-driven organisation.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Quality Assurance Specialist in Bracknell
✨Tip Number 1
Network like a pro! Reach out to professionals in the quality assurance field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on GxP frameworks and quality systems. We recommend practising common interview questions related to compliance and risk management, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just wait for job openings to pop up! Be proactive and reach out to companies you admire, even if they’re not advertising roles. We love seeing candidates take the initiative – it shows passion and commitment.
✨Tip Number 4
Finally, apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always on the lookout for talented individuals who can help us drive quality and compliance forward.
We think you need these skills to ace Senior Quality Assurance Specialist in Bracknell
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that align with the Senior Quality Assurance Specialist role. Highlight your knowledge of GxP frameworks and any relevant quality systems you've worked with, as this will show us you're a great fit for the position.
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 your background in life sciences or healthcare makes you the ideal candidate. Don’t forget to mention specific experiences that demonstrate your problem-solving skills and ability to drive compliance.
Showcase Your Analytical Skills:Since this role involves monitoring compliance and identifying risks, make sure to include examples of how you've used your analytical skills in past roles. We want to see how you’ve contributed to quality improvements and managed multiple priorities in a dynamic environment.
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to submit all your documents in one go. Plus, it shows us you’re serious about joining our team!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Quality Systems
Make sure you brush up on your knowledge of GxP frameworks and quality systems. Be ready to discuss how you've implemented or improved these in past roles. This shows you're not just familiar with the theory but can apply it practically.
✨Prepare for Scenario Questions
Expect questions that ask you to describe how you've handled deviations, CAPAs, or change control in previous positions. Use the STAR method (Situation, Task, Action, Result) to structure your answers clearly and effectively.
✨Show Your Analytical Skills
Be prepared to demonstrate your analytical and problem-solving skills. You might be asked to analyse a hypothetical compliance issue or suggest improvements to a quality process. Think through your approach and be ready to explain your reasoning.
✨Build Relationships
Since this role involves acting as a quality advisor, highlight your experience in building strong relationships across teams. Share examples of how you've collaborated with cross-functional teams to drive compliance and quality improvements.
