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- Tasks: Conduct testing and ensure compliance of pharmaceutical products in a GMP environment.
- Company: Join a leading pharmaceutical manufacturer based in Liverpool, exporting to over 20 countries.
- Benefits: Enjoy professional development, ongoing training, and career progression opportunities.
- Why this job: Be part of a supportive team making a real impact on global health through quality assurance.
- 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 and compliance.
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.
Quality Control Analyst employer: Kenton Black
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, especially HPLC. If you can demonstrate your hands-on experience or knowledge of these methods during an interview, it will show that you're well-prepared and serious about the role.
✨Tip Number 2
Research the company’s products and their compliance with GMP regulations. Being able to discuss their product range and how they maintain quality standards will impress the interviewers and show your genuine interest in their operations.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, particularly those who work in quality control. Engaging with them on platforms like LinkedIn can provide insights into the role and may even lead to referrals, which can significantly boost your chances of landing the job.
✨Tip Number 4
Prepare to discuss your experience with regulatory guidelines such as MHRA, FDA, and ICH. Highlighting your familiarity with these standards during the interview will demonstrate your readiness to comply with industry regulations and contribute to the company's success.
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 pharmaceutical environments. Emphasise your proficiency with analytical techniques like HPLC and any 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 skills in analytical testing and adherence to regulatory guidelines.
Highlight Relevant Skills: In your application, clearly outline your technical skills, such as operating analytical instruments and performing equipment calibration. This will show the employer that you have the hands-on experience they are looking for.
Showcase Continuous Learning: Mention any ongoing training or professional development you've undertaken related to quality control or pharmaceutical sciences. This demonstrates your commitment to staying updated in the field.
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 problem-solving scenarios. Think of examples from your experience where you successfully handled Out of Specification (OOS) results or contributed to method validation.
✨Showcase Your Attention to Detail
As a QC Analyst, attention to detail is paramount. Prepare to provide examples that highlight your meticulous nature, whether it’s through accurate documentation or ensuring compliance with internal quality standards.
