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- Tasks: Ensure pharmaceutical products meet safety and compliance through rigorous analytical testing.
- Company: Join a leading GMP-accredited pharmaceutical manufacturer based in Liverpool, exporting globally.
- Benefits: Enjoy professional development, ongoing training, and career progression in a supportive team.
- Why this job: Be part of a mission-driven company that values quality and compliance in healthcare.
- Qualifications: BSc in Chemistry or related field; 1-3 years in a GMP lab; HPLC proficiency required.
- Other info: Ideal for detail-oriented individuals passionate about pharmaceutical quality.
The predicted salary is between 30000 - 42000 £ per year.
Our client is a well-established, sterile GMP-accredited pharmaceutical manufacturer based in Liverpool, known for producing high-quality pharmaceutical products for both UK and international markets, exporting products to over 20 countries worldwide. Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with advanced analytical techniques? If so, we want to hear from you!
As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.
The responsibilities of the QC Analyst include:
- Conduct routine and non-routine testing of raw materials and finished pharmaceutical products.
- Operate and maintain analytical instruments including HPLC, GC, ICP, wet chemistry and titrations.
- Assist in the introduction and validation of new methods and equipment.
- Assist laboratory manager and technical managers in the capacity as a technical specialist providing advice and technical detail for routine analysis.
- Perform equipment calibration and ensure accurate documentation.
- Assist in the investigation and documentation of Out of Specification (OOS) and Out of Trend (OOT) results.
- Ensure strict adherence to cGMP and internal quality standards.
- Compile, interpret, and report analytical data for R&D and regulatory purposes.
The ideal candidate for the QC Analyst post will have:
- BSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
- 1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
- Proficient in HPLC; experience with other analytical chemistry techniques is advantageous.
- Strong attention to detail and ability to work independently.
- Familiarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.
In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business.
Contact Detail:
Kenton Black Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Analyst
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and GC. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Research the company’s products and their markets. Understanding what they produce and where they export can help you tailor your conversation and show genuine interest in their operations during the interview.
✨Tip Number 3
Brush up on your knowledge of cGMP regulations and relevant guidelines like MHRA and FDA. Being well-versed in these standards will not only boost your confidence but also impress the interviewers with your commitment to quality compliance.
✨Tip Number 4
Prepare examples from your previous experience that highlight your attention to detail and problem-solving skills, especially in relation to OOS and OOT results. This will help you illustrate your capability to handle challenges in a QC environment.
We think you need these skills to ace Quality Control Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control and analytical techniques. Emphasise your proficiency with HPLC and any other analytical methods you've used, as well as your familiarity with GMP regulations.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceutical quality and compliance. Mention specific experiences that demonstrate your ability to thrive in a GMP-regulated environment and your attention to detail.
Highlight Relevant Skills: In your application, clearly outline your skills related to the job description, such as conducting routine testing, operating analytical instruments, and understanding regulatory guidelines. Use examples to illustrate your expertise.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a QC Analyst role.
How to prepare for a job interview at Kenton Black
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of HPLC, GC, and other analytical techniques mentioned in the job description. Be prepared to discuss your hands-on experience with these methods and how you've applied them in previous roles.
✨Understand GMP Regulations
Since this role is in a GMP-regulated environment, it's crucial to demonstrate your understanding of Good Manufacturing Practices. Familiarise yourself with relevant guidelines from MHRA, FDA, and ICH, and be ready to explain how you've adhered to these standards in your past work.
✨Prepare for Technical Questions
Expect technical questions related to quality control processes and troubleshooting OOS/OOT results. Think of specific examples from your experience where you successfully resolved issues or improved processes, as this will showcase your problem-solving skills.
✨Showcase Your Attention to Detail
As a QC Analyst, attention to detail is paramount. During the interview, provide examples that highlight your meticulous nature, such as how you ensure accurate documentation or how you approach equipment calibration and maintenance.
