QA Analyst
Aussicht: 135
Update Tag: 16-11-2025
Ort: Brussels Brussels Capital
Kategorie: IT - Software IT - Hardware / Netzwerk Informationstechnologie Geschäftsführung Produktion / Betrieb
Industrie:
Jobinhalt
QA Analyst Leading Medical Device CompanyMy client is an exciting company that has build a strong international name in their industry.
Work with an energetic manager that runs the team with flexibility and enjoy the company’s autonomous culture. You won’t be dealing with micromanagement, which gives you the opportunity to have more ownership over your work.
The position offers 50% working remotely. Meaning you will save cost and time normally spent on commuting. This will also improve your work/life balance. Giving you more moments to spend with family, friends and hobbies.
Benefits :
2 QA people in the team
Learn from your colleagues
Share your opinions
Receive training onsite
You will do future internal audits
This will mean great career progression
Responsibilities :
You will be working collaboratively with a range of key stakeholders, both within the local team of departments, production and quality at the manufacturing site, distributors, the end users and global and project teams.
You are responsible for the effectiveness and continual improvement of the QMS
You will be working with the registration, administrative functions and analysis of any trends associated with the customer feedback management system for product complaints for the UK/EMEA regions, with back up for the APAC region;
You will also be conducting tasks in accordance with the applicable international standard and internal processes, the Quality Assurance Analyst provides operational support, and input and output information to the Senior Manager QA EMEA-APAC
Requierements :
You have a suitable educational level to undertake quality and customer focused activities.
You know how to work a high level in written and F2F tasks, with report writing abilities to degree level
You have a combination of relevant degree or diploma, with >3-years of Quality/QSHE experience.
You need to have a minimum two years of experience in an ISO/FDA regulated environment (PPE or pharmaceutical).
You have a minimum two years of experience working with a Management System.
You have extensive Internal Auditing experience.
You can demonstrate how to conduct external Auditing experience (ISO, FDA or Customer for example) desirable.
You have advanced knowledge and skills in using Adobe Acrobat, Microsoft applications, including SharePoint, Word, Excel, PowerPoint, CRM, ERPs.
Your knowledge of Quality Assurance theory and practice is great
You have excellent communication and interpersonal skills;
Highly detail-oriented and organized with the ability to multitask in a fast-paced environment.
You have strong analytical skills
You have the ability to critically analyze and make independent decisions and recommendations.
You have strong customer focus orientation both internally and external stakeholders
You need to be fluent in English both written and verbal, and a second language (great if you know French or German) both written and verbal.
If this job appeals to you please apply here or on the NonStop Consulting website or send it to me, Gilson Heitinga, on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.
NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.
Frist: 31-12-2025
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