At a Glance
- Tasks: Ensure compliance and quality in veterinary product distribution with 3rd party manufacturers.
- Company: Join Elanco, a leader in veterinary medicine with a commitment to quality.
- Benefits: Competitive salary, inclusive culture, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on continuous improvement and collaboration.
- Why this job: Make a real impact on animal health by ensuring product quality and compliance.
- Qualifications: Degree in Science or 10 years experience in GMP roles; strong QA background required.
The predicted salary is between 60000 - 75000 £ per year.
To ensure that 3rd Party Manufacturers and Logistics Service Providers (LSPs) are effective and compliant with the relevant regulatory and internal requirements, thereby ensuring that the veterinary medicinal and biocidal products released onto the market are fit for their intended purpose. To drive and maintain improvements in the quality systems and processes, related to 3rd party manufactures, Suppliers and Logistic Service Providers. To provide advice on all quality and compliance matters to ensure retention of the Product and Distribution Licenses.
Your responsibilities:
- Support the qualification and onboarding of Third Parties and Logistics Service Providers in line with GMP/GDP and global quality standards
- Provide Quality input for product launches, qualification, and validation activities
- Manage and support change controls with external partners and internal stakeholders
- Support regulatory submissions and GDP inspections
- Maintain and implement Quality Agreements with suppliers and logistics partners
- Monitor supplier and LSP performance metrics to proactively identify compliance risks
- Support investigations, CAPAs, and quality issue resolution with Third Parties
- Coordinate audits and follow‑up actions with suppliers and logistics providers
- Review Product Quality Reviews (PQRs/APRs) and monitor quality trends
- Drive continuous improvement initiatives across quality systems and supplier oversight activities
What You Need to Succeed (minimum qualifications):
- Degree in Science (Diploma, Master’s degree or equivalent) or minimum 10 years equivalent experience in GMP role
- Minimum 5 years’ experience in Quality Assurance within Distribution GDP regulated environments
- Strong knowledge of GMP, GDP, and regulatory requirements for medicinal products
- Experience working with external manufacturers, suppliers, or distribution partners
- Experience within a global organisation and cross‑functional environment
- Excellent communication skills and strong command of English
What will give you a competitive edge (preferred qualifications):
- Additional language skills
- Knowledge of Quality Control processes
Senior Quality Associate Elanco External Manufacturing (EEM) EMEA (Distribution) in Liverpool employer: Dormont Manufacturing Co
Elanco is an exceptional employer that prioritises employee growth and development within a collaborative and inclusive work culture. Located in the EMEA region, we offer our Senior Quality Associates the opportunity to engage with cutting-edge quality systems while ensuring compliance in the veterinary medicinal sector. Our commitment to continuous improvement and support for professional advancement makes Elanco a rewarding place to build a meaningful career.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Quality Associate Elanco External Manufacturing (EEM) EMEA (Distribution) in Liverpool
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Dormont Manufacturing Co. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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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 Dormont Manufacturing Co.
✨Leverage Internships for Full-time Roles
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✨Tailor Your Approach
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We think you need these skills to ace Senior Quality Associate Elanco External Manufacturing (EEM) EMEA (Distribution) 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 Dormont Manufacturing Co!
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 Dormont Manufacturing Co 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 Dormont Manufacturing Co!
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 Dormont Manufacturing Co, 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 Dormont Manufacturing Co
✨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 Dormont Manufacturing Co 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 Dormont Manufacturing Co’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.
