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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 product delivery across the UK.
- 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: Be part of a team that values innovation and quality in pharmaceutical development.
The predicted salary is between 43200 - 72000 £ 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
Contact Detail:
RBW Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Control Laboratory Manager
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in quality control and analytical chemistry. Attend industry conferences or local meetups to connect with potential colleagues and learn about the latest trends and challenges in QC.
✨Tip Number 2
Familiarise yourself with the specific regulatory requirements and guidelines relevant to the pharmaceutical sector, such as GMP and pharmacopoeia standards. This knowledge will not only enhance your understanding but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your previous experiences in managing teams and overseeing method validation processes. Be ready to share specific examples of how you handled challenges in QC and how you contributed to successful outcomes in your past roles.
✨Tip Number 4
Stay updated on the latest advancements in analytical techniques like HPLC and GC. Being knowledgeable about new technologies and methodologies can set you apart from other candidates and show your enthusiasm for continuous learning in the field.
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 your understanding of the full validation lifecycle. Mention how your previous experiences align with the responsibilities of the role and how you can contribute to the company's growth.
Highlight Relevant Experience: When detailing your work history, focus on your previous roles in QC management or supervision. Include specific examples of method validation activities you've led and any challenges you've overcome in a laboratory setting.
Showcase Leadership Skills: Since this role requires team leadership, be sure to include examples of how you've successfully managed teams in the past. Discuss your approach to supporting team members, especially during out-of-specification challenges.
How to prepare for a job interview at RBW Consulting
✨Showcase Your Leadership Skills
As a Quality Control Laboratory Manager, you'll need to demonstrate your ability to lead and manage a team effectively. Prepare examples of how you've successfully led teams in the past, focusing on your approach to problem-solving and team motivation.
✨Understand Regulatory Standards
Familiarise yourself with the relevant regulatory standards and guidelines in the pharmaceutical industry. Be ready to discuss how you have ensured compliance in previous roles, particularly in relation to method validation and quality control processes.
✨Highlight Technical Expertise
Make sure to emphasise your technical experience with analytical techniques such as HPLC and GC. Be prepared to discuss specific projects where you applied these methods, including any challenges you faced and how you overcame them.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities, especially regarding out-of-specification challenges. Think through potential scenarios and how you would handle them, demonstrating your analytical thinking and decision-making skills.
