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) (Cataluña)
🏢 Kymos Group
📍 Cataluña