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- Tasks: Join us as a QC Analyst to test and analyse pharmaceutical products.
- Company: Be part of a leading global healthcare company innovating medicines and vaccines.
- Benefits: Enjoy a competitive salary of £15.64 per hour and gain valuable industry experience.
- Why this job: Contribute to impactful healthcare solutions while working in a dynamic team environment.
- Qualifications: A relevant degree or equivalent experience in Quality Control is required.
- Other info: This is a 6-month contract role based in Worthing with potential for extension.
CK Group are recruiting for a QC Analyst, to join a company in the pharmaceutical industry, at their site based in Worthing, on a contract basis, initially for 6 months until October 2025. Salary: £15.64 per hour PAYE.
QC Analyst Role:
- To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets.
- Calibrate and maintain analytical equipment.
- Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc).
- To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
- To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date.
- Daily liaison with both other analysts and team leader regarding testing and test results.
- May be required to communicate with the relevant Value Stream to progress OOS investigations.
Your Background:
- A bachelor's degree in a relevant field or equivalent work experience.
- Previous experience working in a Quality Control role in the pharmaceutical industry would be preferable.
- GMP and/or GLP experience.
Company: Our client is one of the largest global healthcare companies researching, developing and supplying innovative medicines, vaccines and healthcare products with their global headquarters in the UK. They invest around £1bn in research and development in the UK annually.
Location: This role is based at our client's site in Worthing.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 129 405 in all correspondence. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
QC Analyst employer: CK Group
Contact Detail:
CK Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC and Karl Fischer. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
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 expectations, which you can leverage in your discussions.
✨Tip Number 3
Prepare to discuss your understanding of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP). Highlighting your knowledge in these areas will show that you are committed to maintaining high safety and quality standards.
✨Tip Number 4
Be ready to talk about your experience with Out of Specification (OOS) investigations. Sharing specific examples of how you've handled such situations in the past will illustrate your problem-solving skills and ability to work collaboratively with team leaders and other departments.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and requirements of the QC Analyst position. Highlight key skills such as experience with HPLC and GMP/GLP knowledge that are essential for the role.
Tailor Your CV: Customise your CV to reflect your relevant experience in Quality Control, particularly in the pharmaceutical industry. Emphasise any specific analytical techniques you have used and your familiarity with safety and GLP standards.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the job requirements. Mention your degree, relevant work experience, and how you can contribute to maintaining high safety and quality standards.
Follow Application Instructions: Ensure you include the job reference number (129 405) in your application. Double-check that all required documents are attached and that your application is submitted through our website for consideration.
How to prepare for a job interview at CK Group
✨Know Your Analytical Techniques
Familiarise yourself with the analytical techniques mentioned in the job description, such as HPLC and Karl Fischer. Be prepared to discuss your experience with these methods and how you've applied them in previous roles.
✨Understand Quality Control Standards
Brush up on Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Demonstrating your knowledge of these standards will show that you are serious about maintaining quality and safety in your work.
✨Prepare for OOS Investigations
Think about any Out of Specification (OOS) investigations you've been involved in. Be ready to explain the process you followed, the challenges you faced, and how you communicated findings with your team or management.
✨Showcase Team Collaboration Skills
Since the role involves daily liaison with other analysts and team leaders, be prepared to discuss examples of how you've successfully worked in a team environment. Highlight your communication skills and ability to collaborate effectively.
