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For Companies At a Glance
- Tasks: Conduct routine and non-routine analysis using advanced techniques like HPLC and GC.
- Company: Join a leading CRO/CDMO in Durham, making waves in pharmaceuticals and biotech.
- Benefits: Gain hands-on experience in a dynamic environment with potential for growth.
- Why this job: Be part of a team contributing to innovative drug development and quality assurance.
- Qualifications: Degree in Chemistry or equivalent experience; prior analytical testing experience required.
- Other info: Exciting opportunity for those passionate about science and quality control.
The predicted salary is between 30000 - 42000 £ per year.
Job Description
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.
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The Role
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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
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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
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If you’d like further information, please contact Graham at CY Partners.
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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 the pharmaceutical and biotech sectors. This knowledge can help you tailor your responses in interviews and show your genuine interest in their work.
✨Tip Number 3
Prepare to discuss your experience with GMP compliance and method validation. Be ready to provide examples of how you've ensured quality and accuracy in your previous roles, as this is crucial for a QC Analyst position.
✨Tip Number 4
Network with professionals in the industry, especially those who work in QC roles. Engaging with them on platforms like LinkedIn can provide insights into the company culture and potentially lead to referrals.
We think you need these skills to ace QC Analyst
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and requirements of the QC Analyst position. Highlight key skills such as experience with analytical techniques and GMP compliance in your application.
Tailor Your CV: Customise your CV to reflect your relevant experience in analytical testing environments. Emphasise your degree in Chemistry and any specific techniques you have used, such as HPLC or GC.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality control and your attention to detail. Mention how your background aligns with the company's focus on pharmaceuticals and biotech.
Proofread Your Application: Before submitting, carefully proofread your application materials for any errors. Ensure that your communication is clear and professional, as this reflects your attention to detail.
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
As a QC Analyst, attention to detail is crucial. Prepare examples from your past work where your meticulous nature helped prevent errors or improved results. This will show your potential employer that you take quality seriously.
✨Communicate Clearly
Effective communication is key in this role. Practice explaining complex analytical results in simple terms, as you may need to present findings to colleagues or management who may not have a technical background.
✨Understand GMP Compliance
Familiarise yourself with Good Manufacturing Practices (GMP) and be ready to discuss how you've ensured compliance in your previous roles. Highlight any experience you have with equipment qualification and method validation.
