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- Tasks: Review analytical data and support QC testing schedules in a dynamic lab environment.
- Company: Join a leading global energy job board with a focus on exciting career opportunities.
- Benefits: Enjoy competitive salary, generous leave, pension scheme, and free parking.
- Other info: Stable long-term career growth with a supportive quality team.
- Why this job: Make a real impact in pharmaceutical manufacturing while building your career.
- Qualifications: 5-8 years in Quality Control and strong attention to detail required.
The predicted salary is between 34000 - 36000 £ per year.
We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
£34,000 – £36,000 per annum (depending on experience)
Permanent | Full Time | Monday to Friday
Benefits:
- 21 days annual leave plus UK bank holidays, with additional annual leave based on length of service (up to 4 extra days).
- Statutory pension scheme, 7 days paid sick leave, Time Off in Lieu (TOIL) and free parking.
- Stable long-term career opportunities and development support.
Key Responsibilities:
- Review analytical data generated from QC testing activities.
- Support planning and coordination of QC testing schedules.
- Review data from HPLC, UV, FTIR and Karl Fischer analysis.
- Support compliance with ALCOA++ principles, data integrity and GMP requirements.
- Assist with laboratory investigations including OOS, OOT and deviations.
- Review documentation in line with quality and regulatory standards.
- Support method validation and adherence to ICH and 21 CFR requirements.
- Work collaboratively across QC and wider site functions.
What We’re Looking For:
- 5–8 years’ experience in Quality Control review or laboratory support.
- Experience reviewing analytical data in pharmaceutical or regulated laboratories.
- Familiarity with Chromeleon or similar laboratory software desirable.
- Understanding of data integrity, GMP and compliance requirements.
- Strong attention to detail and documentation skills.
- Ability to support planning and prioritisation of QC activities.
Desirable:
- Experience with OOS/OOT investigations.
- Exposure to method validation activities.
- Degree in Chemistry, Pharmacy or related scientific discipline.
Why Join Us?
- Competitive salary.
- Secure permanent employment.
- Supportive quality team.
- Opportunity to build your career in regulated pharmaceutical manufacturing.
Apply now to join our Quality team.
Senior QC Reviewer / Planner in NN7, Weedon Bec, West Northamptonshire employer: Energy Jobline CVL
Contact Detail:
Energy Jobline CVL Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Reviewer / Planner in NN7, Weedon Bec, West Northamptonshire
✨Tip Number 1
Network like a pro! Reach out to professionals in the energy sector, especially those working in QC roles. Use platforms like LinkedIn to connect and engage with them; you never know who might have the inside scoop on job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Make sure you can discuss your experience with HPLC, UV, and other analytical techniques confidently. We want you to shine when it comes to showcasing your skills!
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your career goals. Check out our website for tailored job listings in the energy sector. We’ve got some fantastic opportunities waiting for you!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Senior QC Reviewer / Planner in NN7, Weedon Bec, West Northamptonshire
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior QC Reviewer / Planner role. Highlight your relevant experience in Quality Control and any specific skills that match the job description, like familiarity with HPLC or GMP compliance.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for our team. Mention your passion for quality control and how your background aligns with our mission at StudySmarter.
Showcase Your Attention to Detail: Since this role requires strong documentation skills, make sure your application is free from typos and errors. A well-organised application reflects your attention to detail, which is crucial in QC 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’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Energy Jobline CVL
✨Know Your QC Basics
Make sure you brush up on your knowledge of Quality Control principles, especially ALCOA++ and GMP requirements. Being able to discuss these concepts confidently will show that you’re serious about the role and understand the industry's standards.
✨Familiarise Yourself with Analytical Techniques
Since the job involves reviewing data from HPLC, UV, FTIR, and Karl Fischer analysis, it’s crucial to have a solid understanding of these techniques. Prepare to discuss how you've used them in past roles or how you would approach them in this position.
✨Prepare for Scenario Questions
Expect questions about handling OOS/OOT investigations or method validation. Think of specific examples from your experience where you successfully navigated these challenges, as this will demonstrate your problem-solving skills and attention to detail.
✨Show Your Collaborative Spirit
This role requires working closely with various teams. Be ready to share examples of how you’ve collaborated effectively in the past. Highlighting your teamwork skills will help convey that you’re a good fit for their supportive quality team.