Quality, Regulatory and Vigilance

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Come frame our expertise

We are responsible for ensuring the safety of our patients throughout the entire life cycle of our products. We register, monitor and assess quality and regulatory compliance to ensure the marketability of our products. We maintain our quality management system through document management, audits, training and inspections.


Looking for a strategic environment? 
Do you enjoy managing, adapting and advising? Coordinate decision-making in support of a varied product range. With a presence in all 4 corners of the world, you'll be able to challenge yourself in the face of different international regulations and respond to local specificities.


You have a scientific background with a specialization in regulatory affairs or quality, or a background in pharma, bio or chemistry:

• Take charge of regulatory files and the choice of service providers for the management of our product portfolio.
• Be our reference expert for launching and maintaining our product ranges on the market.
• Ensure the quality of products brought to market.
• Maintain a regulatory and scientific watch on our products.

Join us!
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Career opportunities

• Implement quality processes and regulatory obligations at head office and in all our subsidiaries, in liaison with the various departments and suppliers. If you are a product/system/complaints quality manager or supplier auditor, join us.
 

• Guarantee the regulatory compliance and quality of pharmaceutical products, ensuring their safety and efficacy for the well-being of patients. Acting as an intermediary between the scientific teams and regulatory affairs, ensure that products comply with all legal and regulatory requirements, If you are a Regulatory Affairs Manager, join us.
 

• Lead a regulatory strategy around our products in compliance with the rules defined by the regulatory authorities. If you're a regulatory compliance officer or a regulatory affairs manager, discover a market where the rules are changing for both product classes and international standards.
 

• Come face to face with reality in the field, collecting and analyzing feedback from practitioners and patients on the use of our products. If you are in charge of vigilance and medical information, define and monitor the risk management plan, join us.

Join us!
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Discover other Théa professions

The Quality, Regulatory and Vigilance professions would not be possible without close collaboration with the R&D and Medical Affairs teams. These teams work upstream to develop innovative medical solutions, while you ensure that each product meets the most stringent regulatory requirements and safety standards.
 

As a member of the R&D and Medical Affairs teams, you will participate in the search for new therapeutic approaches, and work with experts from a wide range of backgrounds to turn these ideas into concrete solutions. Together, we cover the entire innovation cycle, from research to market launch.
 

Discover the R&D and Medical Affairs professions