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- Tasks: Support quality management and ensure compliance in a dynamic healthcare environment.
- Company: Leading firm in the Pharmacovigilance sector with a focus on patient safety.
- Benefits: Competitive salary, full training, and opportunities for professional growth.
- Why this job: Join a mission-driven team dedicated to maintaining high-quality standards in healthcare.
- Qualifications: 1-2 years in a quality-focused role, preferably in pharmaceuticals or healthcare.
- Other info: Collaborative work culture with a strong emphasis on compliance and patient safety.
The predicted salary is between 24000 - 30000 £ per year.
Our client is a market leader within the Pharmacovigilance sector. They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years’ experience in a quality-focused position, preferably within the pharmaceutical or healthcare industry.
The successful candidate will play a key role in maintaining our Quality Management System (QMS), supporting audits, document control, and ensuring compliance with ISO 9001, Good Pharmacovigilance Practice (GVP), and regulatory requirements. Full training will be provided to build and strengthen ISO 9001 knowledge where required.
Patient safety and compliance are at the very heart of everything our client does, and the Quality Associate will work collaboratively with internal teams, clients, and external stakeholders to ensure the highest quality standards are maintained.
Unfortunately they are unable to offer visa sponsorship.
Quality Associate in Milton Keynes employer: Aspire Personnel Ltd
Contact Detail:
Aspire Personnel Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Associate in Milton Keynes
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already working in quality roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO 9001 and Good Pharmacovigilance Practice. We want you to feel confident discussing how you can contribute to maintaining high-quality standards.
✨Tip Number 3
Showcase your attention to detail! During interviews, share examples of how you've maintained quality in previous roles. This will demonstrate that you’re the right fit for a quality-focused position.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Quality Associate in Milton Keynes
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Associate role. Highlight any relevant experience in quality management or compliance, especially if you've worked in the pharmaceutical or healthcare sectors. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance and how your background makes you a great fit for our team. Don’t forget to mention your attention to detail and organisational skills – they’re key for this role!
Showcase Your Knowledge: If you have any knowledge of ISO 9001 or Good Pharmacovigilance Practice, make sure to mention it! Even if you’re not an expert yet, showing that you’re eager to learn and grow in these areas will impress us. We love candidates who are proactive about their professional development.
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy and ensures your application goes directly to us. Plus, you’ll get to see more about our company culture and values while you’re at it!
How to prepare for a job interview at Aspire Personnel Ltd
✨Know Your Quality Standards
Familiarise yourself with ISO 9001 and Good Pharmacovigilance Practice (GVP) before the interview. Being able to discuss these standards confidently will show that you understand the importance of compliance in the role.
✨Showcase Your Organisational Skills
Prepare examples from your previous experience that highlight your organisational abilities. Discuss how you managed documents or supported audits, as this will demonstrate your attention to detail and ability to maintain a Quality Management System.
✨Emphasise Team Collaboration
Since the role involves working with various teams and stakeholders, be ready to share instances where you successfully collaborated with others. This will illustrate your teamwork skills and your commitment to maintaining high-quality standards.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to quality management and patient safety. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your values.
