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For Companies At a Glance
- Tasks: Lead validation activities and ensure compliance in pharmaceutical manufacturing.
- Company: Leading pharmaceutical manufacturer in Merseyside with a strong quality focus.
- Benefits: Competitive salary, career growth, and a chance to make a real impact.
- Why this job: Join a dynamic team and drive modern validation practices in a vital industry.
- Qualifications: 3+ years in validation, degree in Life Sciences or Engineering preferred.
- Other info: Opportunity to mentor a team and contribute to continuous improvement initiatives.
The predicted salary is between 43000 - 62000 £ per year.
A leading pharmaceutical manufacturer in the Merseyside / North Liverpool area is seeking an experienced Validation Manager to join their Quality function. This is a key role within a well‑established site, supporting a broad range of validation activities and driving a modern, compliant validation approach across the facility.
The Opportunity
Reporting into the QA & Compliance Manager, you will take ownership of the site’s validation programme, ensuring all activities align with the Validation Master Plan and current industry standards. You will work closely with cross‑functional teams, support new product introductions, and play a vital role in inspection readiness and continuous improvement.
Key Responsibilities of the Validation Manager
- Lead the planning, execution, and documentation of site validation activities in line with the Validation Master Plan, covering cleaning, process, mixing, filling, and re‑validation.
- Oversee ICH Q3D Elemental Impurities and PDE/HBEL assessments, ensuring compliance with current regulatory expectations.
- Conduct risk assessments, deviation reviews, and CAPA evaluations from a validation perspective, ensuring robust GMP compliance.
- Provide validation expertise to support NPD/NPI projects, regulatory submissions, and cross‑functional change controls.
- Contribute to inspection readiness, continuous improvement initiatives, and the development of a modern validation culture, while leading and mentoring a small team.
The ideal candidate will have:
- Strong background in pharmaceutical manufacturing validation.
- Degree in a Life Sciences or Engineering discipline (advantageous).
- Minimum of 3 years’ hands‑on validation experience.
- Proven expertise in ICH Q3D Elemental Impurities and PDE assessments.
- Solid understanding of GMP and modern validation principles.
- Experience supporting change controls, deviations, and continuous improvement.
- Confident communicator able to influence across departments and manage competing priorities.
Validation Manager in Knowsley employer: Nexus Life Sciences
Contact Detail:
Nexus Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Manager in Knowsley
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in validation or quality roles. A friendly chat can lead to insider info about job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH Q3D and GMP principles. We recommend creating a cheat sheet with key points and examples from your experience to showcase your expertise during the interview.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or call can show your enthusiasm and keep you on the radar of hiring managers.
✨Tip Number 4
Showcase your leadership skills! If you've mentored others or led projects, be sure to highlight these experiences. Employers love candidates who can drive teams towards continuous improvement and compliance.
We think you need these skills to ace Validation Manager in Knowsley
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Validation Manager role. Highlight your experience in pharmaceutical manufacturing and any specific validation projects you've led. We want to see how your background aligns with our needs!
Showcase Your Skills: In your cover letter, don’t just list your qualifications; showcase your skills! Talk about your hands-on validation experience and how you’ve contributed to compliance and continuous improvement in previous roles. This is your chance to shine!
Be Clear and Concise: When writing your application, keep it clear and concise. Use bullet points where possible to make it easy for us to read through your achievements and experiences. We appreciate a straightforward approach!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to submit all the necessary documents in one go. Let’s get your application in!
How to prepare for a job interview at Nexus Life Sciences
✨Know Your Validation Stuff
Make sure you brush up on your knowledge of validation processes, especially in pharmaceutical manufacturing. Be ready to discuss ICH Q3D Elemental Impurities and how they relate to compliance. This shows you’re not just familiar with the theory but can apply it practically.
✨Showcase Your Leadership Skills
As a Validation Manager, you'll be leading a small team. Prepare examples of how you've successfully led projects or mentored others in the past. Highlight your ability to influence across departments and manage competing priorities – this will demonstrate your readiness for the role.
✨Prepare for Scenario Questions
Expect questions that put you in hypothetical situations related to risk assessments or CAPA evaluations. Think through your approach to these scenarios beforehand, so you can articulate your thought process clearly during the interview.
✨Emphasise Continuous Improvement
The job description mentions continuous improvement initiatives. Be prepared to discuss specific examples where you've contributed to such efforts in previous roles. This will show that you’re proactive and aligned with the company’s goals for modern validation practices.
