Quality Assurance Specialist
Quality Assurance Specialist

Quality Assurance Specialist

Bingham Full-Time 36000 - 60000 £ / year (est.) No home office possible
M

At a Glance

  • Tasks: Support quality assurance activities and ensure compliance with industry standards.
  • Company: Join Medichecks, the UK's first direct-to-consumer blood testing company, revolutionising healthcare.
  • Benefits: Enjoy hybrid working, flexible hours, 25 days holiday, and free health tests for you and your family.
  • Why this job: Be part of a passionate team dedicated to improving lives through innovative healthcare solutions.
  • Qualifications: 2 years in Medical Device & IVD industry; knowledge of ISO standards required.
  • Other info: Opportunity for career growth in a top-rated SME employer.

The predicted salary is between 36000 - 60000 £ per year.

The Role

The Role: Quality Assurance Specialist (Med Devices and IVDs)

Hours: Full Time, Permanent

Salary: £30k – £35k (depending on experience)

Location: Hybrid* (Head office Nottingham)

Must have experience working in Medical Device & IVD industry

Medichecks Group launched the UKs first direct-to-consumer blood testing company in the UK and created a market where there was none. As well as the continued growth of our B2C business we now see considerable opportunity to grow in the B2B and B2B2C space through our technology platform, Plasma.

Our vision is to be part of everyone’s journey to better health. At Medichecks Group we’re building a healthcare platform for the future. We’re a team of medics, designers, engineers and communicators who are intent on bringing our vision to life. We’d like to hear from people who want to use their skills and knowledge to improve peoples’ lives and help us create real change in the way that blood testing and insights can be delivered.

We are proud to be an employer of choice: listed by Best Company in the top 100 SME companies to work for in the UK, top 50 in the East Midlands and top 10 Health and Social Care.

Purpose of this role

This is a new position within a growing team contributing to the quality culture of Medichecks Group. This role will offer development opportunities as you grow into the role and would be perfect for a candidate who already has quality experience and wants to develop their career within the industry even further.

The primary function of this role is to support the Quality and Regulatory team on a day-to-day basis to ensure coordination and compliance of quality activities across all areas of the business, ensuring policies and procedures are fully documented to support compliance and regulatory requirements.

A key element of this role will be focused on the co-ordination of Quality Assurance activities across all areas of the business whilst supporting the management of Medichecks Quality Management System. You will champion continuous improvement of Medichecks processes and contribute to the management and implementation of quality initiatives.

Role and responsibilities

  • Support the maintenance, continual improvement, and audit readiness of the ISO 13485 accredited Quality Management System (QMS).
  • Ensure compliance with national and international standards and legislation, including ISO 13485 and ISO 27001.
  • Manage Corrective and Preventive Actions (CAPA) and non-conformances from logging through to resolution, including root cause analysis and effectiveness checks.
  • Prepare and present monthly trend reports on CAPAs and non-conformances to senior stakeholders.
  • Actively monitor and remain up to date with changes to industry standards, regulations, and guidance.
  • Review, update, and maintain Standard Operating Procedures (SOPs) to ensure QA processes are current, accurate, and clearly communicated to relevant teams.
  • Act as a Subject Matter Expert (SME) for non-conformance and CAPA processes, providing best-practice guidance and refresher training as needed.
  • Administer and manage change controls within the Q&R team from initiation to sign-off.
  • Support the preparation and execution of internal and external audits, contributing as an SME where required.
  • Review and maintain supplier documentation within the QMS, ensuring compliance and currency.
  • Maintain back-ups of QMS and supplier documentation in SharePoint in alignment with Medichecks QMS (MasterControl).
  • Carry out administrative activities within the eQMS to support audit preparation, reporting, and close-out of findings.
  • Develop and maintain Quality & Regulatory (QARA) department FAQs, ensuring they remain accurate and accessible.
  • Communicate with key stakeholders to ensure departmental adherence to relevant SOPs.
  • Identify opportunities to improve or streamline QMS processes and escalate proposals to the Senior Quality & Regulatory Manager.

Skills and Experience

Essential

  • 2 years of experience within the Medical Device & IVD industry.
  • Good working knowledge of industry standards and regulations ISO 13485, IVDR, UK MDR.
  • Experience working to an established QMS.
  • Direct experience of CAPA and non-conformance logging and trending.
  • Prioritisation of workload and well organised with task management.
  • Good communication skills interacting with stakeholders at all levels.
  • Confident presentation skills to present to stakeholders when required.
  • Confidently use Excel/reporting tools available to you to create summary reports of key KPI’s and quality objectives within the business
  • A supportive team player who’s happy to step in, try new things, and ask for help when needed.

Desirable

  • Experience working with an eQMS system. (e.g. Mastercontrol, Q-Pulse)
  • Internal Auditor experience and/or qualification.
  • Experience in maintaining and collating critical supplier documentation.

Medichecks people, perks and culture

We have adopted a flexible hybrid approach to working in both the office and at home, having seen the benefits of both for everyone during the last year. You will predominantly work from home, but sometimes we will get together to collaborate, or for 121s.

We offer flexible working around our core business hours and trust you to work enough hours to do your job well, at times that suit you and your team.

We are committed to making Medichecks a great place to work and have shaped our people strategy around our colleagues’ feedback and we are continuously reviewing this. As well as a competitive salary and the chance to make a real impact in an organisation, here\\\’s a taste of some of the things we offer.

  • 25 days of glorious holidays, plus all of the bank holidays
  • The option to buy and sell holiday
  • Hybrid working- working anywhere from the UK
  • Flexi lunch breaks – grab lunch with a friend or hit the gym
  • Enhanced maternity and paternity leave, as part of our family friendly policies
  • Enhanced paid sickness leave
  • Free and discounted Medichecks blood tests for you and your family and friends
  • Free access to an online GP service
  • Free eye tests and flu jabs
  • Access to discounts and freebies through our reward platform
  • 2 days of paid leave to give some of your time to a charity or community of your choice

#J-18808-Ljbffr

Quality Assurance Specialist employer: Medichecks

Medichecks Group is an exceptional employer, recognised as one of the top 100 SME companies to work for in the UK, offering a vibrant work culture that prioritises employee well-being and development. With a hybrid working model based in Nottingham, employees enjoy flexible hours, competitive salaries, and numerous benefits including enhanced leave options and free health services, all while contributing to meaningful advancements in healthcare technology.
M

Contact Detail:

Medichecks Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Assurance Specialist

✨Tip Number 1

Familiarise yourself with ISO 13485 and other relevant regulations. Understanding these standards will not only help you in the interview but also demonstrate your commitment to quality assurance in the medical device industry.

✨Tip Number 2

Network with professionals in the medical device and IVD sectors. Attend industry events or join online forums to connect with others who can provide insights or even refer you to opportunities at Medichecks.

✨Tip Number 3

Prepare to discuss your experience with CAPA and non-conformance processes. Be ready to share specific examples of how you've managed these in previous roles, as this will be crucial for the Quality Assurance Specialist position.

✨Tip Number 4

Showcase your collaborative skills during the interview. Medichecks values teamwork, so be prepared to discuss how you've successfully worked with cross-functional teams to improve quality processes in the past.

We think you need these skills to ace Quality Assurance Specialist

ISO 13485
IVDR
UK MDR
Quality Management System (QMS)
Corrective and Preventive Actions (CAPA)
Non-conformance logging and trending
Root Cause Analysis
Audit preparation and execution
Stakeholder communication
Presentation skills
Excel and reporting tools proficiency
eQMS system experience (e.g. MasterControl, Q-Pulse)
Internal Auditor experience or qualification
Supplier documentation management
Organisational skills
Collaboration and teamwork

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in the Medical Device and IVD industry. Focus on relevant roles, responsibilities, and achievements that align with the Quality Assurance Specialist position.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of ISO 13485 and other relevant standards. Mention specific examples of how you've contributed to quality management systems in previous roles.

Highlight Relevant Skills: Emphasise your skills in CAPA processes, non-conformance management, and your ability to communicate effectively with stakeholders. Use concrete examples to demonstrate your capabilities.

Show Enthusiasm for Continuous Improvement: Express your commitment to continuous improvement in your application. Discuss any initiatives you've led or participated in that improved quality processes or compliance in your previous positions.

How to prepare for a job interview at Medichecks

✨Know Your Standards

Familiarise yourself with ISO 13485 and other relevant regulations before the interview. Being able to discuss these standards confidently will show your understanding of the industry and your commitment to quality assurance.

✨Showcase Your Experience

Prepare specific examples from your past roles that demonstrate your experience with CAPA processes and non-conformance management. Highlight how you contributed to improvements in quality management systems.

✨Be Ready for Scenario Questions

Expect scenario-based questions where you may need to explain how you would handle certain quality assurance challenges. Practising these scenarios can help you articulate your thought process clearly.

✨Engage with the Team Culture

Medichecks values collaboration and continuous improvement. Be prepared to discuss how you work within a team and your approach to fostering a positive quality culture. Show enthusiasm for contributing to their vision of better health.

Quality Assurance Specialist
Medichecks

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

M
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>