At a Glance
- Tasks: Ensure product quality and compliance while driving continuous improvement in manufacturing processes.
- Company: Join Elanco, a leader in animal health with a commitment to quality.
- Benefits: Competitive salary, inclusive workplace, and opportunities for professional growth.
- Other info: Dynamic role with a focus on teamwork and innovation.
- Why this job: Make a real impact on animal health by ensuring the highest quality standards.
- Qualifications: Degree and 5+ years in quality assurance within a pharmaceutical setting.
The predicted salary is between 45000 - 55000 £ per year.
As a Quality Assurance Representative, you will serve as a primary guardian of product quality and regulatory compliance at the Speke site. This role is responsible for the final disposition of materials and products, ensuring every batch meets the required cGMP standards.
As a key member of the cross‑functional Process Team you will provide advice and support on all manufacturing issues, including deviations and change control. You will drive continuous improvement through regular on‑plant Gemba walks and by monitoring trends in quality data. This position ensures the integrity of manufacturing processes and the safety of Elanco’s animal health products.
Your Responsibilities
- Review and release raw materials, intermediates, and finished products.
- Assess batch records, deviations, and ensure compliance with cGMP standards.
- Provide quality guidance on manufacturing issues, change control, and deviations.
- Support operations through on‑plant presence and regular Gemba walks.
- Lead investigations, support audits, and drive effective CAPAs.
- Monitor quality trends and contribute to continuous improvement initiatives.
- Maintain and approve key quality documentation (e.g., SOPs, protocols, agreements).
What You Need to Succeed (minimum qualifications)
- Degree level (or equivalent) with relevant experience (5 years+) working in a pharmaceutical company in a quality‑related function.
What will give you a competitive edge (preferred qualifications)
- Experience in Pharmaceutical or other regulated industry (i.e., food, healthcare).
- Able to demonstrate strong written and oral communication skills.
- Able to demonstrate strong root cause analysis skills.
- Experience in using Electronic Quality Management System software and SAP.
Senior Associate - Quality Assurance in Liverpool employer: Dormont Manufacturing Co
Elanco is an exceptional employer that prioritises the well-being and professional growth of its employees at the Speke site. With a strong commitment to quality assurance in animal health, the company fosters a collaborative work culture where continuous improvement is encouraged through regular Gemba walks and cross-functional teamwork. Employees benefit from comprehensive training opportunities, a supportive environment, and the chance to make a meaningful impact on product safety and compliance.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Associate - Quality Assurance in Liverpool
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We think you need these skills to ace Senior Associate - Quality Assurance 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.
