€1,186 - 3,777 monthly
Number of Applicants
:000+
Will be hired by client
Pharma/medical devices
Belgium
Min. 1 year of experience in QA
open
MindCapture offers a dynamic and rewarding work environment. We have a strong focus on candidates and believe in long-term relationships that thrive on quality contacts and insights into career opportunities. Not only for our candidates, but also for our consultants, recruiters and support staff.
We offer strong compensation packages that reward your abilities, hard work and ingenuity in achieving success. We reward you with competitive wages and offer a strong package with additional legal benefits such as meal vouchers, eco vouchers, high health insurance (DKV) and group insurance. Depending on your seniority, a car may be provided.
We provide personalised training to let you grow in the area of
What you like to do
What you are good at
Where and how you want to have an impact
MindCapture is a talent and consultancy company, providing advanced consultancy solutions to the biotech, pharma, medical devices, IVD, lab, healthcare and the chemical industry.
At MindCapture we are always looking to expand our team with QA experts.
Haven’t found your dream QA job yet? Apply for an open application and we will get in touch with you.
Responsibilities:
You are responsible for quality by monitoring and ensuring that processes and actions are carried out according to the applied quality standards.
You follow written documents such as procedures, protocols and reports concerning the quality systems.
You provide QA support and supervision for risk assessments, deviations, change control, CAPA and validation activities.
You support audits and handle complaint management.
You manage and coordinate the continuous improvement of deviations and CAPAs and ensure the optimisation of all processes in terms of compliance and efficiency.
You participate in the analysis of quality trends.
You ensure that all major issues impacting the quality system are taken into account, managed and addressed in the action plans.
Master’s degree in life sciences.
You have at least 1 year of relevant QA experience.
The pharmaceutical or medical devices QA standards (ISO13485 or GMP) have no secrets for you.
You speak fluently Dutch and English.
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