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 professional growth.
- Other info: 100% site-based role with a focus on audit readiness and team collaboration.
- Why this job: Make a real impact on compliance and system improvements in a vital industry.
- Qualifications: Degree in Chemistry or related field, with strong HPLC and leadership experience.
The predicted salary is between 42000 - 48000 € per year.
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: LinkedIn
Join a leading pharmaceutical company in the North West, where your expertise as a QC Validation & Systems Lead will be valued and impactful. With a strong commitment to employee development, a collaborative work culture, and a focus on compliance excellence, this role offers you the chance to lead a dedicated team while ensuring the highest standards in a GMP environment. Enjoy competitive remuneration and the opportunity to influence key QC systems in a dynamic and supportive setting.
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 and real-life examples of your experience with HPLC systems and validation processes. We want you to showcase your expertise and how you can improve their QC systems!
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in their minds and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their team.
✨Tip Number 4
Check out our website for the latest job openings and apply directly through us. We’re here to help you land that dream job in QC validation and systems, so don’t miss out on the opportunities we have!
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 reflects the specific skills and experiences mentioned in the job description. Highlight your experience with HPLC systems, validation activities, and any leadership roles you've had. We want to see how you fit into our QC Validation & Systems Lead role!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about QC and how your background aligns with our needs. Don’t forget to mention your hands-on experience and your approach to ensuring compliance excellence in a GMP environment.
Showcase Your Technical Skills:Be sure to detail your technical expertise, especially with QC computerized systems like Empower and LabX. We’re looking for someone who can drive CSV and data integrity, so make those skills pop in your application!
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 platform!
How to prepare for a job interview at LinkedIn
✨Know Your Equipment Inside Out
Make sure you brush up on your knowledge of HPLC systems and other QC equipment. Be ready to discuss your hands-on experience with troubleshooting and maintenance, as well as how you've managed the lifecycle of such equipment in a GMP environment.
✨Showcase Your Leadership Skills
Since this role involves providing technical leadership and managing a small team, be prepared to share examples of your previous supervisory experiences. Highlight how you've motivated your team and improved processes in past roles.
✨Be Audit-Ready
Familiarise yourself with the audit process and be ready to discuss how you've ensured compliance and maintained audit readiness in your previous positions. Mention specific instances where you’ve led or supported audits successfully.
✨Master the Validation Process
Understand the full validation lifecycle (IQ/OQ/PQ) and be ready to explain your approach to managing validation activities. Discuss any challenges you've faced and how you overcame them, especially in relation to documentation and deviation investigations.
