At a Glance
- Tasks: Lead quality assurance activities and shape the quality culture in a fast-paced manufacturing environment.
- Company: Expanding pharmaceutical manufacturing business investing in its people and quality function.
- Benefits: Competitive salary, hands-on leadership role, and opportunities for professional growth.
- Other info: Site-based role with occasional travel for internal audits.
- Why this job: Make a real impact on quality performance and develop your leadership skills.
- Qualifications: Experience in Quality Assurance within GMP-regulated environments and strong leadership abilities.
The predicted salary is between 47250 - 57750 £ per year.
I am partnered with a specialist and expanding pharmaceutical manufacturing business that is continuing to invest in both its people and quality function across the UK. The business is now looking to appoint a QA Manager for one of its South East facilities in Surrey. This is a key position within a small, fast paced manufacturing facility and an excellent opportunity to take ownership of the site wide quality systems, while helping shape quality culture and operational standards moving forward.
Acting as the local quality lead, you will oversee all site quality activities, managing a small team whilst remaining hands-on across the full spectrum of quality assurance. The position will have direct responsibility for a small team and will need to have a hands on, coaching leadership style. This role is about far more than day-to-day operational QA. The successful individual will provide oversight of site-wide quality systems, manage priorities across multiple stakeholders, lead internal auditing activities and act as a key quality partner to both operational and leadership teams.
If you are looking for a position where you can genuinely influence quality performance across a manufacturing site, develop a team and become the recognised quality leader within the facility.
Key Experience:
- Strong experience within Quality Assurance in a GMP-regulated pharmaceutical environment
- Previous experience within aseptic or sterile manufacturing is required
- Leadership or management experience, either through direct line management or demonstrable team leadership responsibilities
- Strong working knowledge of quality systems and QMS oversight
- Experienced in conducting and managing internal audits
- Ability to engage effectively with a wide range of stakeholders across operations, quality and site leadership teams
- Proven ability to manage multiple priorities and deliver results in a fast-paced manufacturing environment
- Experience supporting continuous improvement and quality compliance initiatives
Additional Information:
- Site-based position
- Occasional travel to other UK sites for internal auditing activities
Quality Assurance Manager in England employer: RBW Consulting
Join a dynamic healthcare manufacturing site in Trefriw, North Wales, where you can make a significant impact as a Laboratory Supervisor. We offer a supportive and collaborative work culture that prioritises professional growth, with opportunities to lead a dedicated team and influence quality standards. Enjoy a competitive salary, career development prospects, and the chance to work in a beautiful location while contributing to meaningful advancements in laboratory science and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Manager in England
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like RBW Consulting. 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.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like RBW Consulting. 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 is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Quality Assurance Manager in England
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!
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 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!
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, 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
✨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 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’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.
