At a Glance
- Tasks: Manage quality assurance activities and ensure compliance with standards.
- Company: Join a leading UK manufacturer of innovative medical devices with over 30 years of experience.
- Benefits: Enjoy a competitive salary, flexible working hours, and a range of employee perks.
- Why this job: Be part of a collaborative culture that values growth and innovation in healthcare.
- Qualifications: 3+ years in Quality Assurance with knowledge of international medical device regulations.
- Other info: Opportunity to work on impactful projects and develop your skills in a dynamic environment.
The predicted salary is between 19800 - 46200 £ per year.
About us Check you match the skill requirements for this role, as well as associated experience, then apply with your CV below. For over 30 years, Surgical Innovations have proudly designed, developed and manufactured high quality, precision engineered instruments for minimally invasive surgery and are a leading UK manufacturer of medical devices in its respective field. Our success is our people and we currently employ over 100 staff from our head office in Leeds. We place great value on our mutually respective relationships, a workplace which is collaborative and dynamic, and a culture which is inclusive and purposeful. The result; a platform for individual development, growth, and prosperity. As we seek to identify, nurture, and retain talent, we offer competitive benefits packages, continuous training and development opportunities to ensure those joining us on our journey, grow too! Do you want to be part of an organisation that is leading the evolution in delivering sustainable and innovate solutions which advance healthcare? If so, we want to hear from committed and talented people like you, who share our vision and values, to come and join our team. About the Position As Quality Assurance Specialist you will be responsible for the day-to-day quality assurance activities of the business, including document and change controls, CAPA/NCR’s, concessions and customer complaints. You will prioritise your time to effectively contribute to departmental activities to meet planned demands. This role will work collaboratively with the Manufacturing, Quality Control and Purchasing teams within the business to ensure product is released on time and to the correct standards. Responsibilities On a day to day basis your new role will involve: Day-to-day management of QMS (document control, change control, CAPA/NCR, concessions, supplier control, customer complaints) Completion of all environmental, microbiology and routine product sterilisation / validation activities to agreed schedule. Prioritise workloads and throughput to meet business demands Facilitate and uphold the correct application and completion of all quality documentation generated through the business. Completion of final batch release process to meet sales demands Troubleshoot and resolve quality related internal enquires, and issues within the business Participate in external third-party audits acting as QMS SME. Complete trend analysis, reporting and presenting of Quality data at all levels and specifically for management review. Assists in the routine generation of trend analysis and quality data reports and metrics. Support the maintenance and development of the QMS to reach compliance with current standards and regulations. Carry out internal audits to meet the agreed schedule. Develop, improve, and write new processes and SOPs as required Lead on assigned projects to improve quality/regulatory compliance. Assist with regulatory activities where required. Provide QMS related training to support and improve compliance to current standards and regulations. Requirements To be successful in this role you will need to be able to demonstrate the qualifications, experience and skills for the role: Minimum 3 years’ experience in Quality Assurance, working to the requirements for international quality systems for a medical device company, including ISO 13485. Working Knowledge of EU Medical Device Regulation, MDSAP country specific regulations including, FDA regulations (21 CFR 820), Canadian Medical Device Regulations and other international regulations – desirable. Effective communicator with good interpersonal skills and the ability to work in a cross functional team. Strong organisational skills with a keen eye for detail and ability to manage documentation. Good problem-solving ability and commercial awareness Customer oriented/focused and able to develop and maintain good customer relationships What we offer This position offers a competitive salary of up to £33,000, accompanied by a range of benefits including 9 day working fortnight, flexi time, pension, life assurance, income protection, health cash plan, and high street discount scheme. If this sounds interesting and the right challenge for you, we look forward to receiving your application!
Surgical Innovations Ltd | Quality Assurance Specialist employer: Surgical Innovations Ltd
Contact Detail:
Surgical Innovations Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Surgical Innovations Ltd | Quality Assurance Specialist
✨Tip Number 1
Familiarize yourself with ISO 13485 and the EU Medical Device Regulation. Understanding these standards will not only help you in the interview but also show that you're serious about quality assurance in the medical device industry.
✨Tip Number 2
Highlight your experience with CAPA/NCR processes and document control during your conversations. Being able to discuss specific examples of how you've managed these processes can set you apart from other candidates.
✨Tip Number 3
Demonstrate your problem-solving skills by preparing examples of challenges you've faced in previous roles and how you resolved them. This will showcase your ability to troubleshoot quality-related issues effectively.
✨Tip Number 4
Emphasize your teamwork and communication skills. Since this role involves collaboration with various departments, showing that you can work well in a cross-functional team will be crucial.
We think you need these skills to ace Surgical Innovations Ltd | Quality Assurance Specialist
Some tips for your application 🫡
Understand the Company: Take some time to research Surgical Innovations Ltd. Familiarize yourself with their products, values, and company culture. This will help you tailor your application to align with their mission.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in Quality Assurance, particularly in the medical device industry. Mention specific projects or responsibilities that relate to ISO 13485 and EU Medical Device Regulations.
Showcase Your Skills: Clearly outline your skills that are relevant to the role, such as problem-solving abilities, attention to detail, and effective communication. Use examples to demonstrate how you've successfully applied these skills in previous roles.
Tailor Your Application: Customize your cover letter to reflect your understanding of the position and how your background makes you a great fit. Address the specific responsibilities mentioned in the job description and explain how you can contribute to the team.
How to prepare for a job interview at Surgical Innovations Ltd
✨Understand the Quality Management System (QMS)
Make sure you have a solid understanding of QMS principles, especially document control and CAPA/NCR processes. Be prepared to discuss your experience with ISO 13485 and how you've applied these standards in previous roles.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've effectively resolved quality-related issues in the past. Highlight your analytical skills and ability to troubleshoot problems, as this is crucial for the role.
✨Demonstrate Effective Communication
Since the role involves collaboration with various teams, be ready to discuss how you've successfully communicated and worked with cross-functional teams. Share specific instances where your interpersonal skills made a difference.
✨Highlight Your Customer Focus
Emphasize your customer-oriented approach and how you've maintained good relationships with clients. Prepare to discuss any experiences where you addressed customer complaints or feedback effectively.