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- Tasks: As a QC Analyst, you'll test production samples and maintain analytical equipment.
- Company: Join a leading global healthcare company dedicated to innovative medicines and vaccines.
- Benefits: Earn £15.64 per hour with potential for contract extension and valuable industry experience.
- Why this job: Be part of a mission-driven team ensuring safety and quality in healthcare products.
- Qualifications: A bachelor's degree or relevant experience in Quality Control is required.
- Other info: This role is based in Worthing and may require a DBS check.
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 until the end of the year.
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).
- Carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required.
- 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 (Apply online only) in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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QC Analyst employer: CK Group- Science, Clinical and Technical
Contact Detail:
CK Group- Science, Clinical and Technical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst
✨Tip Number 1
Familiarize 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 the interview will demonstrate your suitability for the role.
✨Tip Number 2
Highlight any previous experience you have in a Quality Control role within the pharmaceutical industry. Be prepared to share specific examples of how you've contributed to maintaining GMP and GLP standards in your past positions.
✨Tip Number 3
Show your understanding of the importance of safety and compliance in a QC environment. You might want to prepare to discuss how you ensure adherence to safety protocols and how you keep training records up to date.
✨Tip Number 4
Network with professionals in the pharmaceutical industry, especially those who work in quality control. Engaging with them can provide insights into the company culture and expectations, which can be beneficial during your interview.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the QC Analyst position. Understand the key responsibilities, such as testing production samples and maintaining analytical equipment, to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize any previous experience in Quality Control within the pharmaceutical industry. Mention specific techniques you are familiar with, like HPLC or Karl Fischer, to demonstrate your qualifications.
Showcase Your Education: Clearly state your educational background, especially if you have a bachelor's degree in a relevant field. If you have equivalent work experience, make sure to detail that as well to meet the job requirements.
Follow Application Instructions: When applying, ensure you quote the job reference provided in the listing. Double-check that you have included all necessary documents and that they are formatted correctly before submitting your application through our website.
How to prepare for a job interview at CK Group- Science, Clinical and Technical
✨Know Your Analytical Techniques
Familiarize 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 GMP and GLP Standards
Since the role requires adherence to GMP and GLP, make sure you can articulate your understanding of these standards. Share examples of how you've implemented or followed these practices in your past work.
✨Prepare for OOS Investigations
Be ready to discuss how you would handle Out of Specification (OOS) results. Think of specific instances where you conducted investigations and how you communicated findings with team leaders or QA managers.
✨Emphasize Team Collaboration
Highlight your ability to work collaboratively with other analysts and departments. Prepare examples that showcase your communication skills and how you’ve contributed to a team environment in a QC setting.
