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- Tasks: Design and validate analytical methods while ensuring product quality through inspections and analysis.
- Company: Join a dynamic team in Cardiff, dedicated to excellence in quality control within the pharmaceutical industry.
- Benefits: Competitive salary, potential for career growth, and a collaborative work environment.
- Why this job: Be part of a skilled team making a real impact on product safety and quality.
- Qualifications: A relevant science degree and experience in analytical validation are essential.
- Other info: Limited supervisory opportunities available for those looking to advance their career.
The predicted salary is between 30000 - 40000 £ per year.
This is an exciting opportunity for a Quality Control Analyst to join an experienced team on the South Coast of Wales.
As an Analyst you will:
- Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verification
- Support the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.
The successful QC Analyst will have:
- A relevant science degree or equivalent qualification
- Understanding of current GMP, Health and Safety and COSHH regulations
- Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision
- The ability to take on a limited supervisory role would be an advantage
- Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation
Senior QC Analyst employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior QC Analyst
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who work in quality control. Attend relevant conferences or seminars in Cardiff to meet potential colleagues and learn more about the latest trends in QC.
✨Tip Number 2
Familiarise yourself with the specific analytical methods mentioned in the job description, such as HPLC and UPLC. Consider taking short courses or online tutorials to enhance your skills and demonstrate your commitment to continuous learning.
✨Tip Number 3
Prepare for potential interviews by reviewing common questions related to quality control and analytical validation. Practise articulating your experience with GMP, Health and Safety regulations, and how you've successfully implemented validation protocols in previous roles.
✨Tip Number 4
Showcase your ability to work independently and take on supervisory roles by highlighting relevant experiences in your discussions. Be ready to provide examples of how you've led projects or mentored junior staff in a laboratory setting.
We think you need these skills to ace Senior QC Analyst
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control and analytical methods. Emphasise your understanding of GMP, Health and Safety, and COSHH regulations, as these are crucial for the role.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the requirements listed in the job description. Mention your experience with HPLC/UPLC/UV/GC analytical method validation and how it aligns with the company's needs.
Showcase Your Skills: In your application, clearly outline your skills in designing validation protocols and writing validation reports. Provide examples of your previous work to demonstrate your capabilities.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is essential for a QC Analyst.
How to prepare for a job interview at Smart4Sciences
✨Showcase Your Technical Skills
Be prepared to discuss your experience with HPLC, UPLC, UV, and GC analytical methods. Highlight specific projects where you designed validation protocols or conducted method validations, as this will demonstrate your hands-on expertise.
✨Understand Regulatory Standards
Familiarise yourself with GMP, Health and Safety, and COSHH regulations. Be ready to explain how you've applied these standards in your previous roles, as this knowledge is crucial for a Senior QC Analyst position.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world situations. Think of examples where you had to troubleshoot issues during validation studies or ensure compliance with quality standards.
✨Demonstrate Leadership Potential
Since the role may involve a limited supervisory capacity, be prepared to discuss any leadership experiences you have. Share examples of how you've guided team members or contributed to a collaborative work environment.
