Microbiology Scientist

Kymos-Group; Bellprat; Vor Ort; EUR 35.000 - 52.000; Vollzeit

Zusammenfassung

Kymos Group is seeking a Scientist to join our Microbiology team. You will lead diverse projects for international clients in a GMP environment, promoting autonomy, continuous learning, and internal growth.

The role emphasizes scientific development and collaboration across disciplines. You will design transfer and validation studies, coordinate timelines, and draft GMP documentation while supervising technical staff and analysts.

Qualifikationen

• Experience designing, supervising, and executing analytical transfer and validation studies.
• Ability to coordinate projects and ensure timelines and quality standards.

Aufgaben

• Design, supervise, and execute analytical transfer and validation studies.
• Manage and coordinate projects, ensuring timelines and quality standards.
• Represent projects to clients and maintain clear communication throughout development.
• Draft and review GMP documentation, including protocols, reports, SOPs, and COAs.
• Supervise and support technical staff and analysts during experiments.

Kenntnisse

Analytical skills

Project management

Jobbeschreibung

Working in a CRO means that science does not stop at a single product or a single analytical need.

At Kymos Group, we are looking for a Scientist to join our Microbiology team. As a Scientist, you will have the opportunity to lead projects, work directly with international clients, and continue building your scientific career in an environment that promotes autonomy, continuous learning, and internal growth.

You will become part of a CRO specialized in analytical services for the pharmaceutical and biotechnology industries, where the variety of projects, products, and analytical techniques will allow you to broaden your experience, develop a more comprehensive scientific perspective, and gain visibility with 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.