Working in a CRO means that every project brings new products, challenges, and opportunities to expand your expertise.

At Kymos Group , we are looking for aScientist to join our Quality Control Studies team . In this role, you will coordinate stability studies for a wide range of pharmaceutical products, manage projects independently, and work closely with international clients while continuing to develop your scientific and technical expertise.

You will become part of a CRO specialized in analytical services for the pharmaceutical industry, where the variety of products, projects, and regulatory requirements will allow you to broaden your experience, develop a deeper understanding of product lifecycle management, and gain exposure to different companies across the sector,



all within a GMP environment.

The challenges you will take on:

- Design, supervise, and execute analytical transfer and validation studies.

- Manage and coordinate projects, ensuring compliance with timelines and quality standards.

- Technically represent projects to clients and maintain smooth communication throughout their development.
- Draft and review GMP documentation, including protocols, reports, standard operating procedures, and certificates of analysis.
- Supervise and support technical staff and analysts during experimental execution.

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📌 Quality Control Scientist (Afternoon Shift) (Bellprat)
🏢 Kymos Group
📍 Bellprat