At a Glance
- Tasks: Lead QC systems and equipment validation in a dynamic GMP lab environment.
- Company: Join a long-standing pharmaceutical partner with a commitment to excellence.
- Benefits: Competitive salary, hands-on role, and opportunities for career advancement.
- Other info: Perfect for those who thrive in leadership roles and enjoy technical challenges.
- Why this job: Make a real impact on compliance and quality in the pharmaceutical industry.
- Qualifications: Degree in Chemistry or related field, with strong HPLC experience.
The predicted salary is between 42000 - 48000 € per year.
If you would like to know a bit more about this opportunity, or are considering applying, then please read the following job information.
Are you an experienced QC professional with a passion for equipment validation, data integrity and keeping GMP labs inspection‑ready? One of our long‑standing pharmaceutical partners is expanding and now seeking a QC Validation & Systems Lead to take ownership of QC systems, equipment lifecycles and computerised platforms across a busy GMP environment. This is a hands‑on, senior role with real influence — perfect for someone who thrives on improving systems, leading validation strategy, and ensuring compliance excellence.
What You’ll Be Doing
- Leading the full lifecycle of QC laboratory equipment, especially HPLC systems — from procurement and qualification through to maintenance, change control and retirement.
- Managing and executing validation activities (IQ/OQ/PQ) and overseeing site calibration programmes, including external service providers.
- Acting as system owner for key QC platforms (e.g., Empower, LabX), driving CSV, data integrity and regulatory compliance.
- Maintaining QC equipment and validation status within electronic systems such as LIMS, ensuring audit readiness at all times.
- Authoring and approving validation documentation, leading deviation investigations, impact assessments and CAPAs.
- Providing technical leadership and line management to a small QC systems team, and representing QC during internal and external audits.
The ideal candidate will have:
- Degree (BSc or equivalent) in Chemistry or a related scientific discipline.
- Strong experience using HPLC, including troubleshooting and maintenance, in a GMP‑regulated QC laboratory.
- Team Leadership or supervisory experience.
- Proven background in equipment qualification, validation, calibration and troubleshooting.
- Hands‑on experience with QC computerized systems (Empower, LabX or CDS systems) and solid understanding of CSV and Data Integrity principles.
- Confident communicator with experience supporting audits; previous supervisory experience is beneficial.
Please note: Sponsorship is not available for this role.
QC Validation & Systems Lead in Chester employer: Nexus Life Sciences
Join a leading pharmaceutical partner in the North West, where your expertise as a QC Validation & Systems Lead will be valued and impactful. With a strong focus on employee development, a collaborative work culture, and a commitment to maintaining GMP excellence, this role offers you the chance to thrive in a dynamic environment while ensuring compliance and driving innovation. Enjoy competitive remuneration and the opportunity to lead a dedicated team in a state-of-the-art laboratory setting, making a real difference in the industry.
StudySmarter Expert Advice🤫
We think this is how you could land QC Validation & Systems Lead in Chester
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QC or GMP labs. A friendly chat can lead to insider info about job openings that might not even be advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Make sure you can confidently discuss HPLC systems and validation processes. We want you to shine when they ask about your hands-on experience!
✨Tip Number 3
Showcase your leadership skills! If you've led teams or projects, be ready to share specific examples. Employers love to see candidates who can take charge and drive compliance excellence in a busy 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’re always looking for passionate individuals who are ready to make an impact in the QC field.
We think you need these skills to ace QC Validation & Systems Lead in Chester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience with QC systems and equipment validation. We want to see how your background aligns with the role, so don’t be shy about showcasing your HPLC expertise and any leadership roles you've had.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about QC in a GMP environment and how you can contribute to our team. We love seeing genuine enthusiasm and a clear understanding of the role.
Showcase Your Technical Skills:When filling out your application, make sure to mention your hands-on experience with computerized systems like Empower or LabX. We’re looking for someone who knows their stuff when it comes to data integrity and compliance, so let us know what you’ve done!
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’re considered for the role. Plus, it’s super easy and straightforward!
How to prepare for a job interview at Nexus Life Sciences
✨Know Your Stuff
Make sure you brush up on your knowledge of HPLC systems and GMP regulations. Be ready to discuss your hands-on experience with equipment validation and troubleshooting, as this will show that you’re not just familiar with the theory but can apply it in practice.
✨Showcase Your Leadership Skills
Since this role involves leading a small QC systems team, be prepared to share examples of your previous leadership experiences. Talk about how you've managed teams, resolved conflicts, or improved processes, as this will demonstrate your capability to take charge.
✨Prepare for Technical Questions
Expect questions around validation activities like IQ/OQ/PQ and data integrity principles. Brush up on your understanding of CSV and be ready to explain how you’ve ensured compliance in past roles. This will help you stand out as a knowledgeable candidate.
✨Be Audit-Ready
Since maintaining audit readiness is crucial, think of specific instances where you’ve prepared for audits or handled deviations. Sharing these experiences will highlight your attention to detail and commitment to compliance, which are key for this position.
