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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 environment.
- 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: Opportunity to work with advanced analytical techniques and contribute to global health.
The predicted salary is between 28800 - 43200 £ 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: JR United Kingdom
Contact Detail:
JR United Kingdom 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 compliance with regulatory guidelines like MHRA and FDA. Showing that you understand their market and quality standards can set you apart from other candidates.
✨Tip Number 3
Prepare to discuss any previous experiences you have had with OOS and OOT results. Being able to articulate how you handled these situations will highlight your problem-solving skills and attention to detail.
✨Tip Number 4
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 role and may even lead to referrals.
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 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 Problem-Solving Skills: In your application, provide examples of how you've handled Out of Specification (OOS) results or contributed to method validation. This will demonstrate your ability to work effectively in a regulated environment.
How to prepare for a job interview at JR United Kingdom
✨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 experience with these methods and how you've applied them in previous roles.
✨Understand GMP Regulations
Familiarise yourself with Good Manufacturing Practice (GMP) regulations and how they apply to quality control in pharmaceuticals. Being able to demonstrate your understanding of compliance will show that you're a serious candidate for the role.
✨Prepare for Technical Questions
Expect technical questions related to quality control processes and problem-solving scenarios. Think of examples from your past experience where you successfully handled Out of Specification (OOS) results or implemented new methods.
✨Showcase Your Attention to Detail
Quality control requires a keen eye for detail. Be ready to provide examples of how your attention to detail has positively impacted your work, whether through accurate documentation or meticulous testing procedures.
