Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Analyse pharmaceutical samples and conduct validation studies using advanced analytical techniques.
- Company: Join a leading Pharmaceutical CRO in Oxfordshire, known for its innovative research and development.
- Benefits: Enjoy competitive salary, career progression, and the chance to work in a dynamic environment.
- Why this job: Be part of impactful projects that ensure the highest quality standards in pharmaceuticals.
- Qualifications: Degree in Analytical Chemistry or related field; experience in QC roles and analytical techniques required.
- Other info: Applicants must be eligible to work in the UK; no visa sponsorship available.
The predicted salary is between 36000 - 60000 £ per year.
Pharmaceutical Quality Control Analyst – Validation Location: Oxfordshire Sector: Pharmaceutical Our client is a leading Pharmaceutical CRO based in Oxfordshire and due to continued expansion, they now have an exciting opportunity for an experienced QC Analyst to join the company and support in Validation studies within the analytical team. The role: As a QC Analyst you will be responsible for analysing pharmaceutical samples using a range of analytical techniques and for a variety of projects. This role will focus on: * Validation and verification of analytical methods for HPLC, GC, NMR, KF etc. * Degradation and stability studies for a variety of conditions * LCMS analysis for impurity identification * Running and reporting on multiple projects simultaneously * All work must be carried to the highest quality standards and in compliance with industry guidelines. * You will also be expected to interpret and report on the laboratory work completed. Experience expectations: Suitable applicants; * Previous Pharmaceutical industry experience working in an analytical or QC role is essential * Experienced in the use of analytical techniques such as HPLC, GC, NMR, UV-Vis, FT-IR * Knowledge of Quantitative and Qualitative analysis * Good knowledge of GMP, FDA and MHRA guidelines * Experience with Method Validation and Stability studies * Educated to degree level (or equivalent experience) in Analytical Chemistry, Pharmaceutical Science or Chemistry discipline * Organised and methodical approach to work * Good communication skills The Package: Our client offers an opportunity to work for a leading Pharmaceutical company on a permanent basis with a competitive annual salary, benefits and career progression opportunities. Applicants must be fully eligible to work in the UK. Visa Sponsorship is not available with this position and therefore applicants must not require immediate sponsorship or have Visa sponsorship requirements in the future
Pharmaceutical Quality Control Analyst - Validation employer: Taylorollinson
Contact Detail:
Taylorollinson Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Pharmaceutical Quality Control Analyst - Validation
✨Tip Number 1
Familiarise yourself with the specific analytical techniques mentioned in the job description, such as HPLC, GC, and NMR. Being able to discuss your hands-on experience with these methods during an interview will demonstrate your suitability for the role.
✨Tip Number 2
Stay updated on the latest GMP, FDA, and MHRA guidelines. Showing that you are knowledgeable about current regulations can set you apart from other candidates and highlight your commitment to quality standards.
✨Tip Number 3
Prepare to discuss your previous experience with method validation and stability studies. Be ready to provide examples of how you've successfully managed multiple projects simultaneously, as this is a key aspect of the role.
✨Tip Number 4
Network with professionals in the pharmaceutical industry, especially those working in quality control or analytical roles. Engaging with others in the field can provide valuable insights and potentially lead to referrals for the position.
We think you need these skills to ace Pharmaceutical Quality Control Analyst - Validation
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in the pharmaceutical industry, particularly in analytical or QC roles. Emphasise your familiarity with techniques like HPLC, GC, and NMR, as well as your understanding of GMP, FDA, and MHRA guidelines.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific projects or experiences that demonstrate your skills in method validation and stability studies, and how they align with the job requirements.
Showcase Analytical Skills: When detailing your experience, focus on your analytical skills and any specific projects where you successfully ran and reported on multiple analyses. Use quantifiable achievements to illustrate your impact in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail, which is crucial in this field.
How to prepare for a job interview at Taylorollinson
✨Showcase Your Analytical Skills
Be prepared to discuss your experience with analytical techniques like HPLC, GC, and NMR. Highlight specific projects where you successfully applied these methods, as this will demonstrate your hands-on expertise.
✨Understand Industry Guidelines
Familiarise yourself with GMP, FDA, and MHRA guidelines. During the interview, mention how you have adhered to these standards in your previous roles, showcasing your commitment to quality and compliance.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world scenarios. Think of examples from your past work where you had to troubleshoot issues during validation studies or method development.
✨Communicate Clearly and Effectively
Good communication skills are essential for this role. Practice explaining complex concepts in a straightforward manner, as you may need to report findings to both technical and non-technical stakeholders.
