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- Tasks: Conduct quality control analysis of pharmaceutical products using advanced techniques.
- Company: Join a leading pharmaceutical team in South London with a focus on quality.
- Benefits: Competitive salary, benefits package, and career development opportunities.
- Why this job: Make a real impact in healthcare by ensuring product quality and safety.
- Qualifications: Experience in GMP-compliant labs and strong HPLC skills required.
- Other info: Dynamic team environment with opportunities for growth and training.
The predicted salary is between 36000 - 60000 £ per year.
Location: South London (Fully Site-Based)
Employment Type: Full-Time
About the Role: We are seeking a highly skilled and motivated Quality Control Analyst to join a pharmaceutical team in South London. This is a fully site-based role, ideal for someone with a strong background in analytical chemistry and a passion for maintaining high standards in a GMP-regulated environment.
Key Responsibilities:
- Perform routine and non-routine analysis of raw materials and finished pharmaceutical products using HPLC (essential), GC, UV, and FTIR techniques (preferred).
- Demonstrate advanced troubleshooting skills with HPLC systems and lead Out of Specification (OOS) investigations.
- Ensure all testing is conducted in compliance with GMP standards and internal SOPs.
- Accurately document results and maintain laboratory records in accordance with regulatory requirements.
- Support method development and validation activities as needed.
- Collaborate with cross-functional teams to resolve quality issues and improve laboratory practices.
Requirements:
- Proven experience in a GMP-compliant pharmaceutical QC laboratory.
- Strong proficiency in HPLC is essential, including troubleshooting and OOS investigations.
- Experience with GC, UV, and FTIR techniques is highly desirable.
- Excellent attention to detail and ability to work independently in a fast-paced environment.
- Strong communication and documentation skills.
What’s on Offer:
- Competitive salary and benefits package.
- Opportunity to work in a dynamic and supportive team.
- Career development and training opportunities.
QC Analyst – Pharmaceuticals in New Malden employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QC Analyst – Pharmaceuticals in New Malden
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that QC Analyst role.
✨Tip Number 2
Prepare for interviews by brushing up on your HPLC and GMP knowledge. We recommend practising common interview questions and even doing mock interviews with friends. Confidence is key!
✨Tip Number 3
Showcase your troubleshooting skills! Be ready to discuss specific examples of how you’ve tackled OOS investigations or improved lab practices. We want to see your problem-solving prowess in action.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace QC Analyst – Pharmaceuticals in New Malden
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in a GMP-compliant pharmaceutical QC lab. We want to see your skills in HPLC and any other relevant techniques like GC or FTIR. Customising your CV to match the job description will help us see why you're the perfect fit!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality control in pharmaceuticals and how your background aligns with our needs. We love seeing enthusiasm and a personal touch, so don’t hold back!
Showcase Your Attention to Detail: In a QC role, attention to detail is key. When writing your application, make sure to highlight specific examples of how you've maintained high standards in previous roles. We want to know how you ensure compliance with GMP standards and internal SOPs!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you get all the updates. Plus, it shows us you're keen on joining our team at StudySmarter!
How to prepare for a job interview at RBW Consulting
✨Know Your Techniques
Make sure you brush up on your knowledge of HPLC, GC, UV, and FTIR techniques. Be ready to discuss your hands-on experience with these methods, especially HPLC troubleshooting and OOS investigations, as they are crucial for the role.
✨Understand GMP Standards
Familiarise yourself with Good Manufacturing Practice (GMP) regulations and how they apply to quality control in pharmaceuticals. Be prepared to explain how you've ensured compliance in your previous roles and how you would maintain high standards in this position.
✨Showcase Your Attention to Detail
Quality control is all about precision. During the interview, provide examples of how your attention to detail has positively impacted your work. Discuss specific instances where your meticulousness helped avoid errors or improved laboratory practices.
✨Communicate Effectively
Strong communication skills are essential for collaborating with cross-functional teams. Practice articulating your thoughts clearly and concisely. Think of examples where you successfully resolved quality issues through effective teamwork and communication.