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- Tasks: Manage product complaints, conduct internal audits, and oversee document control.
- Company: Join a fast-paced medical device company in Bradford with a strong reputation.
- Benefits: Potential for permanent position, gain valuable experience in a regulated industry.
- Why this job: Perfect for detail-oriented individuals looking to make an impact in quality control.
- Qualifications: Experience in ISO 13485 or similar industries like cosmetics or pharmaceuticals preferred.
- Other info: Initial temporary role of 6 weeks with potential for extension.
The predicted salary is between 30000 - 42000 £ per year.
We have an immediate temporary opportunity for a Quality Associate based in Bradford, working with a well-established and fast-paced medical device company. This role is for an initial minimum period of 6 weeks, with the potential to extend or go permanent for the right candidate. We are looking for someone with ideally ISO 13485. If you do not have experience specifically linked to medical devices then experience of a similar nature in the cosmetic or pharmaceutical industry would be considered.
This is a fantastic opportunity for someone with strong product quality control experience ideally within the medical device industry, who is confident working independently and can hit the ground running. The successful candidate will take ownership of key quality processes including complaints handling, internal audits, and document control.
You need to have a strong eye for detail, confidence managing regulated quality systems, and the ability to problem-solve under pressure. You'll need to work well both independently and as part of a team, with a proactive approach and good communication across departments.
Responsibilities:- Managing product complaints: investigation, documentation, follow-up and risk management
- Carrying out internal audits to ensure compliance with ISO 13485 and company procedures
- Overseeing document control processes
Contact Detail:
Click To Hired Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Associate
✨Tip Number 1
Familiarise yourself with ISO 13485 standards if you haven't already. Understanding these regulations will not only boost your confidence but also demonstrate your commitment to quality management in the medical device industry.
✨Tip Number 2
Network with professionals in the medical device field. Attend industry events or join relevant online forums to connect with others who can provide insights and potentially refer you to opportunities at companies like us.
✨Tip Number 3
Prepare to discuss specific examples of how you've handled product complaints or conducted audits in previous roles. Being able to articulate your problem-solving skills under pressure will set you apart from other candidates.
✨Tip Number 4
Showcase your ability to work independently and as part of a team during interviews. Highlight experiences where you've successfully collaborated with different departments to improve quality processes, as this aligns with our expectations for the role.
We think you need these skills to ace Quality Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality control, particularly within the medical device, cosmetic, or pharmaceutical industries. Emphasise any familiarity with ISO 13485 and specific achievements that demonstrate your attention to detail.
Craft a Compelling Cover Letter: Write a cover letter that showcases your understanding of the role and the company. Mention your problem-solving skills and ability to manage regulated quality systems, as well as your proactive approach to work.
Highlight Relevant Skills: In your application, clearly outline your skills related to complaints handling, internal audits, and document control. Use specific examples to illustrate how you've successfully managed these processes in previous roles.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Quality Associate role.
How to prepare for a job interview at Click To Hired
✨Showcase Your Attention to Detail
As a Quality Associate, having a strong eye for detail is crucial. Be prepared to discuss specific examples from your past experiences where your attention to detail made a significant impact on quality control or compliance.
✨Demonstrate Your Knowledge of ISO 13485
Since the role requires familiarity with ISO 13485, make sure you brush up on its key principles. Be ready to explain how you've applied these standards in previous roles, even if they were in the cosmetic or pharmaceutical industries.
✨Prepare for Problem-Solving Scenarios
The ability to problem-solve under pressure is essential. Think of situations where you faced challenges in quality management and how you resolved them. Practising these scenarios can help you articulate your thought process during the interview.
✨Emphasise Your Communication Skills
Good communication across departments is vital in this role. Prepare to discuss how you've effectively communicated with different teams in the past, especially when handling complaints or conducting audits.
