At a Glance
- Tasks: Oversee supplier quality across EMEA, ensuring compliance and product quality.
- Company: Join a leading pharmaceutical company committed to innovation and quality.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on continuous improvement and career development.
- Why this job: Make a real impact on product quality and patient safety in a dynamic environment.
- Qualifications: Bachelor's degree and 3 years' experience in a GxP-regulated setting required.
The predicted salary is between 45000 - 60000 £ per year.
Reporting to the Manager, Supplier Quality Management (EMEA), this role is responsible for the quality oversight of suppliers across the EMEA region.
The successful candidate will manage supplier quality activities throughout the supplier lifecycle, including qualification, quality risk management, change control, and issue resolution.
Using a risk-based approach, the role supports compliance with Gx P requirements, company standards, and regulatory expectations while working collaboratively with suppliers and cross-functional stakeholders to ensure product quality, regulatory compliance, and continuity of supply.
Key Responsibilities
- Manage supplier qualification, onboarding, periodic review, and ongoing oversight activities in accordance with Gx P requirements and company standards.
- Review and assess supplier quality documentation, including change notifications, deviations, investigations, CAPAs, regulatory inspection outcomes, and quality metrics.
- Evaluate supplier changes, quality events, and compliance issues using a risk-based approach to determine potential impact on product quality, patient safety, regulatory compliance, and continuity of supply.
- Partner with suppliers and internal stakeholders to investigate and resolve supplier quality issues in a timely manner.
- Establish, review, and maintain Supplier Quality Agreements with suppliers and service providers.
- Collaborate with Quality, Manufacturing, Technical Services, Regulatory Affairs, Procurement, Supply Chain, and other business functions to support supplier-related activities.
- Apply quality risk management principles and sound scientific judgement to support quality decisions and supplier oversight activities.
- Contribute to continuous improvement initiatives within the Supplier Quality Management program.
Qualifications
- Bachelor's degree in Science, Engineering, Quality, or a related discipline.
- Minimum 3 years' experience in a Gx P-regulated environment.
- Experience within the pharmaceutical, biotechnology, vaccine, medical device, or related industries.
- Knowledge of supplier quality management, quality systems, change control, deviations, investigations, CAPA, and quality risk management.
- Understanding of applicable global regulations and Gx P requirements.
- Experience reviewing supplier quality documentation and assessing quality and compliance risks.
- Strong analytical, communication, stakeholder management, and problem-solving skills.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.
Benefits
- For more information on CSL benefits visit
- Equal Opportunity Employer
CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit
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Sr. Specialist, Supplier Quality Management (EMEA) in Liverpool employer: CSL
As an Associate Director in Procurement Enablement at CSL, you will be part of a forward-thinking organisation that prioritises sustainability and governance while fostering a culture of continuous improvement and talent development. With a commitment to employee growth through the Global Procurement Academy and a collaborative work environment, CSL offers a unique opportunity to influence procurement practices on a global scale, making it an excellent employer for those seeking meaningful and impactful careers.
StudySmarter Expert Advice🤫
We think this is how you could land Sr. Specialist, Supplier Quality Management (EMEA) in Liverpool
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like CSL. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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✨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 CSL is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Sr. Specialist, Supplier Quality Management (EMEA) in Liverpool
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 CSL!
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 CSL 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 CSL!
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 CSL, 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 CSL
✨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 CSL 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 CSL’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.
