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- Tasks: Conduct routine and non-routine analysis of materials using advanced techniques.
- Company: Join a leading CRO/CDMO in Durham, making an impact in pharmaceuticals and biotech.
- Benefits: Gain hands-on experience with cutting-edge technology and contribute to innovative projects.
- Why this job: Be part of a dynamic team focused on quality and compliance in a fast-paced environment.
- Qualifications: Degree in Chemistry or equivalent experience; prior analytical/GMP testing experience required.
- Other info: Contact Graham at CY Partners for more details about this exciting opportunity.
The predicted salary is between 36000 - 60000 £ per year.
CY Partners are excited to be supporting a leading CRO/CDMO in Durham who are looking for a Quality Control Analyst to join their QC team. This is a fantastic opportunity to work across pharmaceuticals, biotech and fine chemicals, contributing to GMP manufacture of novel APIs and other specialist materials. The Role Routine and non-routine analysis of raw materials, intermediates & finished products Use of HPLC, GC, UV-Vis, FTIR, NMR & wet chemistry techniques Method development, validation & stability studies Supporting equipment qualification and GMP compliance Clear communication of results to colleagues & management About You Degree in Chemistry (or equivalent experience) Prior experience in an analytical/GMP testing environment Strong knowledge of analytical techniques & method validation Excellent attention to detail, communication, and IT/data integrity skills If you’d like further information, please contact Graham at CY Partners
QC Analyst employer: CY Partners
Contact Detail:
CY Partners 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 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 recent projects or developments in pharmaceuticals and biotech. This knowledge will not only help you understand their work better but also allow you to ask insightful questions during your interview.
✨Tip Number 3
Prepare to discuss your experience with GMP compliance and how you've contributed to maintaining quality standards in previous roles. Highlighting specific examples will show that you are a strong candidate for the QC Analyst position.
✨Tip Number 4
Network with professionals in the industry, especially those who work in quality control or related fields. Engaging with them can provide valuable insights and potentially lead to referrals for the position at StudySmarter.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your degree in Chemistry and any relevant experience in an analytical or GMP testing environment. Emphasise your knowledge of analytical techniques and method validation, as these are crucial for the QC Analyst role.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the position and the company. Mention specific experiences that demonstrate your attention to detail and communication skills, as well as your familiarity with HPLC, GC, UV-Vis, FTIR, NMR, and wet chemistry techniques.
Showcase Relevant Experience: When detailing your previous roles, focus on your routine and non-routine analysis of raw materials and finished products. Highlight any method development, validation, and stability studies you have conducted, as these will be key to the role.
Proofread Your Application: Before submitting your application, carefully proofread all documents to ensure there are no errors. Clear communication is essential, so make sure your writing is concise and professional, reflecting your strong IT and data integrity skills.
How to prepare for a job interview at CY Partners
✨Know Your Analytical Techniques
Make sure you brush up on your knowledge of HPLC, GC, UV-Vis, FTIR, NMR, and wet chemistry techniques. Be prepared to discuss how you've used these methods in previous roles and any specific challenges you faced.
✨Demonstrate Your Attention to Detail
Quality Control Analysts need to have a keen eye for detail. During the interview, provide examples of how your attention to detail has positively impacted your work, especially in a GMP environment.
✨Communicate Clearly
Since clear communication of results is crucial, practice explaining complex analytical results in simple terms. This will show that you can effectively communicate with both technical and non-technical colleagues.
✨Prepare for Method Development Questions
Expect questions about method development, validation, and stability studies. Be ready to discuss any relevant experiences and how you approached these tasks in your previous roles.
