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- Tasks: Coordinate and maintain validation programmes across manufacturing and packaging operations.
- Company: Join a leading UK pharmaceutical manufacturer focused on quality and compliance.
- Benefits: Gain valuable experience in a regulated environment with career growth opportunities.
- Why this job: Make a real impact by ensuring product quality and compliance in a dynamic industry.
- Qualifications: Life science degree and experience in QA, QC, or Validation preferred.
- Other info: Work collaboratively with cross-functional teams in a supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
AssureBio is partnering with a UK-based pharmaceutical manufacturer to appoint a QA Validation Coordinator into a technically strong Quality & Regulatory function. This role is ideal for a detail-driven QA or Validation professional who enjoys working across manufacturing, QC, engineering, and regulatory teams, owning validation frameworks that underpin compliant, reliable product supply. If you like turning complex data into clear validation evidence, this is a role where your work directly supports QA and inspection readiness.
Responsibilities
- Support technical QA leadership by coordinating and maintaining site-wide validation, qualification, and calibration programmes across manufacturing and packaging operations.
- Be a central point of reference for validation status, historical data, and technical documentation, working closely with QA, QC, Engineering, and Operations.
- Ownership and maintenance of the Validation Master Plan (VMP) and key validation frameworks.
- Coordinating process, cleaning, analytical method, stability and hold-time validation activities.
- Supporting continuous process verification (CPV) and periodic re-validation reviews.
- Managing validation inputs into Annual Product Quality Reviews (APQRs).
- Ensuring validation work reflects routine manufacturing and packaging batches.
- Supporting new product introduction and technical change activities.
- Raising and supporting deviations linked to validation or GMP issues.
Technical Focus Areas
- Manufacturing & packaging process assessment (e.g. blending, granulation, compression, coating, packaging).
- Cleaning validation and contamination control strategies.
- Analytical method validation (non-pharmacopoeial where required).
- Stability study coordination, reporting and trending.
- Statistical analysis and data review (e.g. CpK, trending, datasets).
Key Experience
- Life science degree (or equivalent scientific background).
- Experience across QC, QA, Manufacturing or Validation in a regulated environment.
- Exposure to validation, stability, or technical QA activities.
- Strong data handling and report-writing capability.
- Comfortable coordinating cross-functional technical work.
- Methodical, organised and confident working with complex datasets.
- Experience with validation or statistical software is beneficial but not essential.
Validation Coordinator in London employer: AssureBio
Contact Detail:
AssureBio Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Coordinator in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in QA and Validation roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Be ready to discuss validation frameworks and your experience with data handling. We want you to shine when they ask about your past projects!
✨Tip Number 3
Showcase your problem-solving skills! During interviews, share examples of how you've tackled challenges in QA or Validation. This will demonstrate your ability to think critically and adapt in a regulated environment.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Validation Coordinator in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Validation Coordinator role. Highlight your experience in QA, validation, and any relevant technical skills that match the job description. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Data Skills: Since this role involves handling complex datasets, make sure to highlight your data analysis and report-writing capabilities. Share specific examples of how you've turned data into clear validation evidence in your previous roles.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at AssureBio
✨Know Your Validation Frameworks
Make sure you brush up on the key validation frameworks relevant to the role. Be prepared to discuss how you've previously owned or maintained a Validation Master Plan (VMP) and any specific methodologies you've used in your past roles.
✨Showcase Your Data Skills
Since this role involves turning complex data into clear validation evidence, come ready with examples of how you've handled statistical analysis or data review in previous positions. Highlight any experience with CpK trending or datasets to demonstrate your analytical prowess.
✨Understand Cross-Functional Collaboration
This position requires working closely with QA, QC, Engineering, and Operations teams. Think of instances where you've successfully coordinated cross-functional projects and be ready to share how you navigated challenges and ensured smooth communication.
✨Prepare for Technical Questions
Expect technical questions related to manufacturing and packaging processes, cleaning validation, and analytical method validation. Brush up on these topics and be ready to discuss your experience in a regulated environment, as well as any specific challenges you've faced and how you overcame them.
