Organization description

You will join a community of more than 80 experts in your field; Depending on your level of experience, you will collaborate or lead the management of projects or operational services related to the quality assurance system of various customers (pharma, biotech, medtech), such as:

• Deviations, CAPA, Change Control, OOS management ;
• Supplier management;
• PQR writing/revision;
• Audit management;
• Batch release;
• Training ;
• Data management;
• You propose a continuous improvement plan to create value or be proactive in your mission;
• You take part in tailor-made training courses to develop your general and specific skills;
• You participate in or organize workshops/events to share your knowledge with your peers;
• You monitor your projects and personal development with your Talent Manager and Business Manager.

Our offer

• Degree in a life science related field (preferably);
• First experience in Quality Assurance;
• Experience in the life sciences industry;
• Knowledge of GMP’s;
• Team Player;
• Excellent communication skills (speaking and writing);
• Fluency in English and French or Dutch.

We ask

• Attractive salary in line with the market and your experience;
• Salary package with very competitive extra-legal benefits;
• Optimum work-life balance thanks to 12 ADV days, sliding hours and homeworking possibilities;
• Join a community of over 80 consultants in quality and regulatory affairs, with many social events organized throughout the year;
• Training and workshops to develop/share your skills