At a Glance
- Tasks: Ensure our products meet top quality standards and support continuous improvement.
- Company: Join Corin, a leader in medical technology and innovation.
- Benefits: Competitive salary, bonus, excellent pension, and private medical insurance.
- Other info: Dynamic team with opportunities for career growth and development.
- Why this job: Make a real impact in a highly regulated environment while enhancing your skills.
- Qualifications: Experience in quality assurance and knowledge of GMP regulations required.
The predicted salary is between 40000 - 50000 £ per year.
We’re looking for a proactive QA Quality Engineer to support our Quality Assurance function and ensure our products and processes meet the highest regulatory and quality standards.
What you’ll do:
- Evaluate Manufacturing and Quality processes for compliance with ISO 13485, GMP, and FDA 21 CFR 820.
- Support Quality, Manufacturing and cross‑functional teams with investigations, documentation, and continuous improvement.
- Support continuous improvement to manufacturing process through NCRs, root cause analysis and risk management activities.
- Support internal audits.
- Review/approve SOPs and product/equipment specifications.
- Adhere to Quality Management System (QMS) requirements in line with Corin’s Good Manufacturing Practice (GMP) as per ISO13485 & FDA21 CFR Part 820.
- Work with multiple stakeholders internally; R&D, Operations and Validation plus many others.
- Analyse quality data, support product complaint investigations, and maintain Quality Dashboards/KPIs.
What You’ll Bring:
- Experience in a highly regulated environment e.g. medical devices, pharma, aerospace, automotive.
- Knowledge of upholding core Quality requirements within GMP environment.
- Background in quality, engineering or with manufacturing experience. Degree or HNC/HND in Engineering beneficial (ideally mechanical or biomedical).
- Hands‑on experience in a similar role with quality requirements.
- Knowledge /understanding of core quality concepts such as CAPA, NCRs, revision control, and root cause analysis.
- Strong organisation, analytical thinking, and decision‑making skills.
- Influencing: Develop a network of internal resources to facilitate completion of tasks, ability to challenge and promote high quality output is key.
- Planning and organising: Complete daily work to meet established schedule, re‑prioritise activities to support business needs.
- Driving decision making and making an impact: Exercise authority within pre ‐ established limits and approval.
What's in it for you:
- A competitive salary and a discretionary annual bonus.
- Excellent pension – starts at 6%, going up to 9.7% after 18 months.
- Life assurance – Six times your basic salary.
- Private medical insurance with BUPA for you and your family.
- Free annual eye tests and flu vaccinations.
- Employee referral program where you can earn up to £1,000 for each successful hire you recommend.
Why Corin?
Join a company where technology and innovation improve lives every day. Apply now to be part of our journey.
Corin provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
QA Quality Engineer in Cirencester employer: Corin Group
Corin is an exceptional employer that prioritises innovation and quality in the medical device sector, offering a collaborative work culture where employees are encouraged to contribute to meaningful projects that enhance lives. With competitive salaries, comprehensive benefits including private medical insurance and a robust pension scheme, as well as ample opportunities for professional growth and development, Corin stands out as a rewarding place to build your career in quality assurance.
StudySmarter Expert Advice🤫
We think this is how you could land QA Quality Engineer in Cirencester
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at Corin or similar companies. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of ISO 13485 and GMP standards. We want to see that you’re not just familiar with these concepts but can also discuss how they apply to real-world scenarios.
✨Tip Number 3
Showcase your problem-solving skills! Be ready to share examples of how you've tackled quality issues in the past. We love hearing about your hands-on experience and how you’ve contributed to continuous improvement.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Corin.
We think you need these skills to ace QA Quality Engineer in Cirencester
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the QA Quality Engineer role. Highlight your experience in regulated environments and any relevant qualifications. We want to see how your background aligns with our needs!
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 you can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Skills:Don’t forget to showcase your analytical thinking and decision-making skills in your application. Mention specific examples of how you've influenced quality outcomes in previous roles. We’re all about continuous improvement!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be one step closer to joining our innovative team at Corin!
How to prepare for a job interview at Corin Group
✨Know Your Standards
Familiarise yourself with ISO 13485, GMP, and FDA 21 CFR 820. Being able to discuss these standards confidently will show that you understand the regulatory environment and can contribute to maintaining compliance.
✨Showcase Your Analytical Skills
Prepare examples of how you've used root cause analysis and risk management in past roles. Be ready to explain your thought process and how your actions led to improvements in quality or processes.
✨Engage with Stakeholders
Think about how you’ve collaborated with cross-functional teams in the past. Be prepared to share specific instances where you influenced outcomes or facilitated communication between departments.
✨Demonstrate Continuous Improvement Mindset
Come equipped with ideas on how to support continuous improvement initiatives. Discuss any experiences you have with NCRs or CAPA processes, and how you’ve contributed to enhancing quality in previous roles.
