At a Glance
- Tasks: Lead and manage Quality Control activities in a dynamic pharmaceutical environment.
- Company: Join an international advanced pharmaceutical company expanding across the UK.
- Benefits: Competitive salary, career development, and the chance to shape a growing team.
- Other info: Opportunity to build team culture and establish best practices.
- Why this job: Make a real impact by developing a high-performing QC department.
- Qualifications: 3+ years of management experience in a GMP-regulated lab setting.
The predicted salary is between 36087 - 44107 £ 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 solid understanding of the full validation lifecycle is essential, alongside strong regulatory knowledge and an analytical chemistry background. Whilst this will not be a hands-on role day to day, given the size of the unit, you will need to be comfortable spending time in the laboratory and supporting the team, particularly with out-of-specification investigations, method development, and validation activities.
A strong laboratory background is essential, with experience in equipment maintenance, troubleshooting, and validation highly desirable. This is an excellent opportunity for an experienced people leader to help shape and develop a growing QC function. With approximately 75% of the team being newly recruited, you will have a unique opportunity to build team culture, establish best practices, and develop a high-performing department alongside site leadership.
We are ideally looking for someone with around three years' management experience who can bring proven leadership skills and confidently manage the operational and people aspects of the role from day one.
Key Experience
- Experienced QC Manager, Laboratory Manager, QC Supervisor or Senior QC/Analytical Chem professional within a GMP-regulated pharmaceutical environment
- Strong laboratory experience, including equipment maintenance, troubleshooting, and analytical testing oversight
- Experience managing validation activities and supporting method validation programmes
- Technical experience with analytical techniques such as HPLC and/or GC
- Previous people management experience, ideally 3+ years
- Proven ability to lead, develop, and mentor teams
- Strong organisational, planning, and resource scheduling skills
- Excellent understanding of GMP requirements and pharmacopoeial standards
QC Manager employer: RBW Consulting LLP
Join a supportive and growing GMP healthcare manufacturing facility in Trefriw, North Wales, where you will play a pivotal role in overseeing quality assurance and control activities. With a strong emphasis on career development, competitive salary, and a commitment to fostering a robust quality culture, this company offers an excellent environment for experienced professionals looking to make a meaningful impact in their field.
StudySmarter Expert Advice🤫
We think this is how you could land QC Manager
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like RBW Consulting LLP. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like RBW Consulting LLP.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like RBW Consulting LLP. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what RBW Consulting LLP is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QC Manager
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at RBW Consulting LLP!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show RBW Consulting LLP that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at RBW Consulting LLP!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At RBW Consulting LLP, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at RBW Consulting LLP
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at RBW Consulting LLP that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with RBW Consulting LLP’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
