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- Tasks: Lead and manage Quality Control activities, focusing on method development and team oversight.
- Company: Join a growing international pharmaceutical company making waves in the UK market.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and impact.
- Why this job: Make a real difference in QC operations while developing your leadership skills in a supportive setting.
- Qualifications: Experience in QC/Analytical Chemistry management within a GMP environment is essential.
- Other info: This role offers a chance to influence future growth plans and tackle exciting challenges.
The predicted salary is between 36000 - 60000 £ per year.
I am partnered exclusively with an international advanced pharmaceutical company that is continuing to expand operations both in terms of product delivery and site presence across the UK. This specific hire will take management and scheduling responsibilities for all site Quality Control (QC) activities with a strong focus on method development oversight and team leadership. A strong focus on the full validation lifecycle from beginning to end is crucial in combination with solid regulatory understanding from an analytical chemistry perspective.
Whilst this will not be hands-on day to day, given the size of the unit, you will need to be comfortable being in the laboratory and supporting the team, especially with out of specification challenges and development and validation activities. If you are looking for a varied position that offers you a chance to make a real impact on your own site and play the key part in how the QC team delivers both now and for future growth plans, please apply below or contact Mark Bux-Ryan for further information.
Key experience:
- Experienced QC/Analytical Chemistry manager or supervisor within a pharmaceutical GMP environment
- Technical experience will include some of the following – HPLC, GC
- Previous people management experience is essential
- Excellent understanding of pharmacopoeia
- Knowledge and experience of method validation activities from beginning to end
Quality Control Laboratory Manager employer: RBW Consulting
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Laboratory Manager
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in the pharmaceutical industry, especially those related to quality control and analytical chemistry. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the pharmaceutical sector, particularly those who work in quality control or laboratory management. Attend industry conferences or join relevant online forums to connect with potential colleagues and learn about job openings before they are advertised.
✨Tip Number 3
Prepare to discuss specific examples of your leadership experience and how you've successfully managed QC teams in the past. Highlight any challenges you've faced and how you overcame them, as this will showcase your problem-solving skills and ability to lead effectively.
✨Tip Number 4
Be ready to demonstrate your technical expertise in methods like HPLC and GC during the interview process. Brush up on your knowledge of method validation and be prepared to discuss how you've applied these techniques in previous roles to ensure compliance and quality.
We think you need these skills to ace Quality Control Laboratory Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Quality Control and Analytical Chemistry, especially within a pharmaceutical GMP environment. Emphasise your management skills and any specific technical expertise, such as HPLC or GC.
Craft a Compelling Cover Letter: In your cover letter, express your passion for quality control and how your background aligns with the company's goals. Mention your understanding of the full validation lifecycle and your ability to lead a team effectively.
Highlight Relevant Experience: When detailing your work history, focus on your previous roles that involved method validation and people management. Use specific examples to demonstrate your achievements and how they relate to the responsibilities of the QC Laboratory Manager position.
Showcase Regulatory Knowledge: Since a solid regulatory understanding is crucial for this role, make sure to mention any relevant certifications or training you have in pharmacopoeia and regulatory compliance. This will show your preparedness for the challenges of the position.
How to prepare for a job interview at RBW Consulting
✨Showcase Your Technical Expertise
Make sure to highlight your experience with HPLC, GC, and other relevant analytical techniques during the interview. Be prepared to discuss specific projects where you successfully managed method validation activities from start to finish.
✨Demonstrate Leadership Skills
As a QC Laboratory Manager, you'll need to lead a team effectively. Share examples of how you've previously managed teams, resolved conflicts, and motivated staff to achieve their best performance.
✨Understand Regulatory Standards
Familiarise yourself with the latest pharmacopoeia and regulatory requirements in the pharmaceutical industry. Be ready to discuss how you ensure compliance within your team and the importance of these standards in quality control.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills, especially regarding out-of-specification challenges. Think of specific instances where you successfully navigated such issues and be ready to explain your thought process.
