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For Companies At a Glance
- Tasks: Ensure GMP compliance and support the release of high-quality products in a dynamic environment.
- Company: Join a pioneering UK-based bioscience organisation driving innovation in pharmaceuticals.
- Benefits: Competitive salary, growth opportunities, and a collaborative team culture.
- Why this job: Be at the forefront of biotech innovation and make a real impact.
- Qualifications: Degree in Chemistry or related field with strong GMP experience.
- Other info: Exciting career development as the company invests in growth and technology.
The predicted salary is between 36000 - 60000 ÂŁ per year.
Are you a Quality professional with solid GMP experience looking to join an innovative and rapidly growing bioscience organisation? Smart4 Sciences are supporting a pioneering UK-based business who are using their state‑of‑the‑art facility to drive the next generation of products used across pharmaceutical, nutraceutical, and personal‑care markets - and they are now looking to strengthen their QA function with a proactive Senior Quality Assurance Specialist.
The Role
As a key member of the QA team, you'll play a vital role in ensuring site‑wide GMP compliance and supporting the release of high‑quality products. This is a varied and hands‑on role where you'll work closely with manufacturing, QC, and R&D teams in a fast‑paced, collaborative environment.
Key responsibilities include:
- Overseeing batch release and reviewing manufacturing and QC documentation
- Managing the self‑inspection programme and supporting internal/external audits
- Reviewing and approving SOPs, deviations, CAPAs, OOS, and change controls
- Supporting validation and data integrity activities
- Delivering GMP and QA process training across site
- Driving continuous improvement and supporting Quality Management Reviews
About You
You’ll bring:
- A degree in Chemistry or related scientific discipline
- Strong experience within a GMP‑regulated environment
- Excellent understanding of quality systems and risk management
- A practical, solutions‑focused approach to regulatory compliance
- Ideally, experience in manufacturing or QC operations
Why Join?
- Work at the cutting edge of biotech innovation
- Join a business investing over ÂŁ10 million into growth and technology
- Be part of a collaborative, forward‑thinking QA team
- Genuine scope for development as the company continues its expansion
If you're a Quality professional ready to make an impact in a unique and high‑growth bioscience environment, we'd love to hear from you. Apply now or contact Gareth Gooley @ Smart4 Sciences for a confidential discussion.
Senior Quality Assurance Specialist - Pharmaceuticals in Peterborough employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Quality Assurance Specialist - Pharmaceuticals in Peterborough
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical and bioscience sectors. Attend industry events or webinars to meet potential employers and get your name out there. Remember, it’s all about who you know!
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and quality systems. Be ready to discuss real-life scenarios where you've ensured compliance or improved processes. Show them you’re the solutions-focused professional they need!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and fit your expertise. Tailor your approach to each company to stand out!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Share any additional thoughts you have about the role or how you can contribute to their QA team.
We think you need these skills to ace Senior Quality Assurance Specialist - Pharmaceuticals in Peterborough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience mentioned in the job description. Highlight your GMP experience and any relevant quality assurance roles you've had. We want to see how you fit into our innovative team!
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 the bioscience sector. Share specific examples of how you've contributed to compliance and quality improvements in previous roles.
Showcase Your Team Spirit: Since this role involves collaboration with various teams, make sure to mention your teamwork skills. We love candidates who can work closely with manufacturing, QC, and R&D teams to drive quality initiatives forward.
Apply Through Our Website: We encourage you to apply directly 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 updates from us!
How to prepare for a job interview at Smart4Sciences
✨Know Your GMP Inside Out
Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss specific examples from your past experience where you've ensured compliance or improved quality systems. This will show that you’re not just familiar with the concepts but can apply them effectively.
✨Showcase Your Collaborative Spirit
Since this role involves working closely with manufacturing, QC, and R&D teams, be prepared to share examples of how you've successfully collaborated in previous roles. Highlight any cross-functional projects you've been part of and how you contributed to achieving common goals.
✨Prepare for Technical Questions
Expect some technical questions related to batch release processes, SOPs, and CAPAs. Review the key responsibilities listed in the job description and think about how your experience aligns with them. Being able to articulate your understanding of these processes will set you apart.
✨Demonstrate Continuous Improvement Mindset
The company values continuous improvement, so come prepared with examples of how you've driven improvements in quality assurance processes in the past. Discuss any initiatives you've led or been a part of that resulted in enhanced efficiency or compliance.
