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ID SOLUTIONS ?
ID SOLUTIONS is an innovative French company in the fields of oncology and infectiology.
Here, you can find all the current jobs available at ID SOLUTIONS and discover why you should join us.
Founded in 2016, ID SOLUTIONS is located in Grabels, near Montpellier. Since the arrival of the health crisis, it has adapted its know-how to the problem of detecting COVID-19 and its variants. The company develops and produces a range of RT-PCR detection kits for SARS-CoV2 and all its mutants.
The company has also developed and diversified its product range in infectiology, offering detection solutions ranging from intestinal infections to monkeypox via its new iSolutions™ range. To meet the growing demand from laboratories and hospitals, the company’s workforce has tripled in just a few months.
With 70 employees working at our Montpellier and Marseille sites, we aim to be a company on a human scale, enabling everyone to express their full potential.
As we grow, we’re always on the lookout for ambitious, creative and enthusiastic people.
Joining ID SOLUTIONS means taking part in a shared challenge, where team solidarity is at the heart of our values.
WORK FOR ID SOLUTIONS, IT'S ...
Building a healthy corporate culture
Promoting team cohesion
Encouraging team support
Improving working methods
Recruitment process
Step 1 :
Pre-selection phone interview with our HR team
Step 2 :
Interview with the manager in person or by videoconference
Step 3 : Discuss HR issues with our team
Step 4 :
Integration with a dedicated course
Open positions
Quality Assurance Manager M/F
Montpellier
Degree level
Quality and Regulatory Affairs
As a Quality Assurance Officer (M/F), reporting to the Quality Assurance Manager, you will be responsible for implementing and managing the quality system in accordance with the ISO 13485 standard within the applicable regulatory context.
Senior Quality and Regulatory Affairs Manager (M/F)
Montpellier
Master degree level
Quality and Regulatory Affairs
As Senior Quality and Regulatory Affairs Manager (M/F), reporting to the Director of Regulatory, Clinical & Quality Affairs, you will be responsible for ensuring the compliance of processes and products at national and international level, as well as the operational implementation of the company’s regulatory and quality strategy.