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- Tasks: Ensure pharmaceutical products meet safety and compliance through rigorous testing and analysis.
- 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 technical expertise and readiness for the role.
✨Tip Number 2
Research the company’s products and their compliance with regulatory guidelines like MHRA and FDA. Showing that you understand their market and the importance of quality control in their operations can set you apart from other candidates.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, especially those who work in quality control. Engaging with them on platforms like LinkedIn can provide insights into the company culture and may even lead to a referral.
✨Tip Number 4
Prepare to discuss specific examples of how you've handled Out of Specification (OOS) results or contributed to method validation in previous roles. This will showcase your problem-solving skills and your ability to maintain compliance in a GMP 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 GMP-regulated environments. Emphasise your proficiency with analytical techniques like HPLC and any specific achievements in previous roles.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceutical quality and compliance. Mention specific experiences that demonstrate your skills in analytical testing and adherence to regulatory guidelines.
Highlight Relevant Qualifications: Clearly state your educational background, particularly your BSc in Chemistry or Pharmaceutical Sciences. Include any additional certifications or training related to quality control and GMP practices.
Showcase Attention to Detail: In your application, provide examples of how you have demonstrated strong attention to detail in your work. This could include instances where you successfully identified OOS results or contributed to method validation.
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 methods mentioned in the job description. Be prepared to discuss your experience with these techniques and how you've applied them in previous roles.
✨Understand GMP Regulations
Familiarise yourself with Good Manufacturing Practices (GMP) and relevant regulatory guidelines like MHRA and FDA. Showing that you understand these regulations will demonstrate your commitment to quality and compliance.
✨Prepare for Technical Questions
Expect technical questions related to quality control processes and analytical testing. Think about specific challenges you've faced in the lab and how you resolved them, as this will showcase your problem-solving skills.
✨Highlight Attention to Detail
As a QC Analyst, attention to detail is crucial. Prepare examples from your past work where your meticulous nature helped prevent errors or improved outcomes. This will help convey your suitability for the role.
