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- Tasks: Promote technical skills and quality standards while sampling and analyzing API and drug products.
- Company: Join a dynamic team focused on quality control in the pharmaceutical industry.
- Benefits: Enjoy a competitive rate, training opportunities, and various employee benefits.
- Why this job: Take ownership of your projects and make a real impact in quality assurance.
- Qualifications: Must have a scientific degree and experience with HPLC, GC, UV, FTIR.
- Other info: This is a 23-month contract with a 36-hour work week.
This is a great opportunity for an experienced QC Analyst to join this world-leading company providing health solutions!
In this role, you will have the opportunity to promote and improve technical skills and quality standards with the QC team. You will also be responsible for sampling, analyzing, and the release of API, drug products, and materials. Additionally, you will hold ownership over your own analytical projects within the team, driving the completion of validation and analytical transfer activities.
This is a 23-month contract, with a 36-hour working week, and a rate of £23 per hour. The company can also provide various benefits and training.
If you have experience in the following, we would love to hear from you:
- Scientific Degree in a relevant subject
- Proven industry experience handling HPLC, GC, UV, FTIR
- Strong GMP Knowledge
- Experience with analytical method validation & principles
Sounds good, how do I apply?
- Option 1: Click the apply button; don’t worry if you don’t have an up-to-date CV, we can discuss whatever you have to hand.
- Option 2: Find Morgan Veness on LinkedIn and drop me a message or connection request.
- Option 3: Drop The One Group Cambridge Office a call and ask for Morgan .
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Senior QC Analyst employer: The One Group
Contact Detail:
The One Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Analyst
✨Tip Number 1
Make sure to highlight your hands-on experience with HPLC, GC, UV, and FTIR during any discussions or interviews. Be prepared to discuss specific projects where you utilized these techniques and the outcomes of those projects.
✨Tip Number 2
Demonstrate your understanding of GMP regulations by preparing examples of how you've implemented these standards in your previous roles. This will show that you not only know the theory but also how to apply it practically.
✨Tip Number 3
Be ready to discuss your experience with analytical method validation. Prepare to explain the steps you took in past projects and any challenges you faced, along with how you overcame them.
✨Tip Number 4
Show your enthusiasm for ownership of projects by sharing examples of when you took the lead on an analytical project. Highlight your ability to drive completion and collaborate with team members to achieve goals.
We think you need these skills to ace Senior QC Analyst
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your experience with HPLC, GC, UV, and FTIR in your CV and cover letter. Provide specific examples of how you've used these techniques in previous roles.
Showcase Your Scientific Degree: Clearly state your scientific degree in your application. If you have any additional certifications or training related to quality control or analytical methods, include those as well.
Demonstrate GMP Knowledge: In your application, illustrate your understanding of Good Manufacturing Practices (GMP). Mention any relevant experiences where you ensured compliance with these standards.
Tailor Your Cover Letter: Craft a personalized cover letter that addresses the specific requirements of the Senior QC Analyst position. Discuss your passion for quality control and how you can contribute to the team's success.
How to prepare for a job interview at The One Group
✨Showcase Your Technical Skills
Be prepared to discuss your experience with HPLC, GC, UV, and FTIR in detail. Highlight specific projects where you utilized these techniques and the outcomes of your analyses.
✨Demonstrate GMP Knowledge
Since strong GMP knowledge is crucial for this role, be ready to explain how you've applied GMP principles in your previous work. Use examples to illustrate your understanding of quality standards.
✨Discuss Analytical Method Validation
Prepare to talk about your experience with analytical method validation. Discuss the principles behind it and any challenges you faced during validation processes, along with how you overcame them.
✨Express Ownership and Initiative
This role involves ownership of analytical projects, so convey your ability to take initiative. Share examples of past projects where you led efforts, drove completion, and ensured quality outcomes.
