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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 in the pharmaceutical industry.
- Qualifications: BSc in Chemistry or related field; 1-3 years in a GMP lab; HPLC proficiency required.
- Other info: Ideal for those passionate about quality control and analytical techniques.
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, 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
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 potentially lead to referrals.
✨Tip Number 4
Prepare to discuss your problem-solving skills, particularly in relation to Out of Specification (OOS) results. Be ready to share examples of how you've handled similar situations in past roles to showcase your analytical thinking.
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 conducting analytical testing and adhering 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 previous roles. This is crucial for a QC Analyst position, so make it stand out.
How to prepare for a job interview at Kenton Black
✨Showcase Your Technical Skills
Be prepared to discuss your experience with analytical techniques like HPLC, GC, and wet chemistry. Highlight specific projects or tasks where you successfully used these skills, as this will demonstrate your hands-on expertise.
✨Understand GMP Regulations
Familiarise yourself with Good Manufacturing Practices (GMP) and relevant regulatory guidelines such as MHRA and FDA. Being able to articulate how you have adhered to these standards in previous roles will impress the interviewers.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities, especially regarding Out of Specification (OOS) results. Think of examples from your past experience where you successfully navigated similar challenges.
✨Demonstrate Attention to Detail
Quality Control requires a keen eye for detail. During the interview, provide examples of how your attention to detail has positively impacted your work, whether in data analysis or documentation accuracy.
