At a Glance
- 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.
- Other info: Experience with HPLC and regulatory guidelines is a plus.
- 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 preferred.
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 in Liverpool employer: Kenton Black
Join a leading pharmaceutical manufacturer in Liverpool, where your expertise as a Quality Control Analyst will be valued in a dynamic and supportive work environment. With a strong commitment to employee growth, ongoing training, and career progression, this GMP-accredited company offers a unique opportunity to contribute to the safety and efficacy of pharmaceutical products while working with advanced analytical techniques. Experience a culture that prioritises quality, compliance, and teamwork, making it an excellent place for professionals seeking meaningful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Control Analyst in Liverpool
✨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 may even lead to referrals.
✨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 practical knowledge will highlight your problem-solving skills and attention to detail.
We think you need these skills to ace Quality Control Analyst in Liverpool
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 your familiarity with regulatory guidelines and how your skills align with the responsibilities of the QC Analyst role.
Highlight Relevant Experience:In your application, detail your experience in conducting routine and non-routine testing, as well as your ability to operate and maintain analytical instruments. Use specific examples to demonstrate 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.
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 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 and be ready to explain how you've adhered to them 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 implemented new methods.
✨Showcase Your Attention to Detail
As a QC Analyst, attention to detail is key. Prepare to provide examples that highlight your meticulous nature, whether it’s through accurate documentation or thorough testing procedures. This will show your potential employer that you take quality seriously.
