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- Tasks: Join us as a QC Analyst to test and analyze pharmaceutical products.
- Company: Be part of a leading global healthcare company innovating medicines and vaccines.
- Benefits: Earn £15.64 per hour with opportunities for growth in a dynamic environment.
- Why this job: Make an impact in healthcare while working with cutting-edge analytical techniques.
- Qualifications: Bachelor's degree or equivalent experience in Quality Control preferred.
- Other info: This is a contract role based in Worthing, UK, 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 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 121 588 in all correspondence.
Please note:
This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check. #J-18808-Ljbffr
QC Analyst employer: Royal Society of Chemistry
Contact Detail:
Royal Society of Chemistry 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 an interview will demonstrate your suitability for the QC Analyst 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
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 may even lead to referrals.
✨Tip Number 4
Prepare for potential questions about OOS investigations and how you would handle them. Understanding the process and being able to articulate your approach will show that you're ready to take on the responsibilities of the role.
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. Highlight key responsibilities such as testing production samples and maintaining analytical equipment, and think about how your experience aligns with these tasks.
Tailor Your CV: Customize your CV to emphasize relevant experience in Quality Control, particularly in the pharmaceutical industry. Include specific examples of your work with analytical techniques like HPLC or Karl Fischer, and any GMP/GLP experience you have.
Craft a Strong Cover Letter: Write a cover letter that showcases your passion for quality control and your understanding of the pharmaceutical industry. Mention your educational background and any previous roles that have prepared you for this position, and express your enthusiasm for contributing to the company's goals.
Follow Application Instructions: When applying, ensure you quote the job reference 121 588 in all correspondence. Double-check that you meet the eligibility requirements to work in the UK and that all your documents are complete before submission.
How to prepare for a job interview at Royal Society of Chemistry
✨Know Your Analytical Techniques
Make sure you are familiar 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, brush up on these standards. Be ready to explain how you have implemented these practices in your past work and why they are crucial in a QC environment.
✨Prepare for OOS Investigations
Think about any Out of Specification (OOS) investigations you've been involved in. Be prepared to discuss specific examples, including how you approached the investigation and what the outcomes were.
✨Emphasize Team Collaboration
This role involves daily communication with other analysts and team leaders. Highlight your teamwork skills and provide examples of how you've successfully collaborated with others to achieve testing goals.
