At a Glance
- Tasks: Lead the QC team to ensure top-notch quality control for medical products.
- Company: Join a globally-connected company making a difference in healthcare.
- Benefits: Enjoy a competitive compensation package and professional growth opportunities.
- Other info: Collaborative culture focused on continuous improvement and customer service.
- Why this job: Make an impact on medical propellants while working in a dynamic environment.
- Qualifications: Extensive QC lab experience and a background in Chemistry are essential.
The predicted salary is between 37800 - 46200 £ per year.
Lead the Medical Products QC Team to maintain a compliant analytical and quality control function supporting manufacturing and sale of Orbia F EM Medical Products. You will oversee analysts, schedules, and equipment to ensure timely analysis and release under cGMP. You will collaborate cross-functionally, host regulatory audits, and drive continuous improvement to strengthen product quality and customer service. This role offers a globally-connected, professional environment and a chance to impact medical propellants and related products.
Pay / Benefits
- Competitive compensation package
Responsibilities
- Manage shift analysts and laboratory staff to deliver timely analysis, reporting, and QA release of cGMP-regulated medical propellants
- Plan analytical schedules to meet production and sales needs; prioritise during peak demand
- Coordinate maintenance and calibration of lab equipment with Team Leaders to minimize production disruption
- Ensure external testing labs meet cGMP standards reflected in the Medical Products QC Team
- Assist in hosting cGMP and quality audits, lead lab tours and address non-conformances
- Oversee stability study activities within the laboratory
- Lead continuous improvement projects in the Medical Propellants Lab to benefit the Medical Business
- Engage with customers and suppliers for method transfer, analytical support, and troubleshooting
- Ensure SHE standards and housekeeping within the Medical QC area
- Support Site Quality Manager with budgeting and monitoring medical QC expenditure
Key requirements
- Extensive experience in a QC Laboratory operating to cGMP standards
- Understanding of QC in the pharmaceutical industry
- Experience managing a QC laboratory, preferably with cGMP
- Minimum: HNC/HND Chemistry; desirable: degree in Chemistry or related subject
- Ability to liaise with regulatory bodies and customers on quality matters
- Develop yourself
- Foster Collaboration Inclusion
- Drive Results
- QC Laboratory management
- cGMP standards
- Analytical method transfer
QC Team Leader employer: Orbia
Wavin, part of Orbia's Building & Infrastructure business, is an exceptional employer that prioritises innovation and employee development in a collaborative environment. Located in Doncaster, we offer a competitive compensation package and a strong commitment to safety and diversity, ensuring that every team member can thrive and contribute to meaningful projects that enhance global infrastructure. Join us to be part of a professional team dedicated to advancing life through sustainable solutions.
StudySmarter Expert Advice🤫
We think this is how you could land QC Team Leader
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Orbia. 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 Orbia.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Orbia. 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 Orbia is looking for. A tailored application can really make you stand out!
We think you need these skills to ace QC Team Leader
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 Orbia!
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 Orbia 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 Orbia!
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 Orbia, 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 Orbia
✨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 Orbia 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 Orbia’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.
