Working in a CRO means that every project brings new products, challenges, and opportunities to expand your expertise.
Es esencial asegurarse de que cumple con los requisitos como solicitante para este puesto; por favor, lea atentamente la información a continuación.

At Kymos Group , we are looking for a Scientist 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:

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- 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.

Requisitos:

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- A university degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.

- Minimum of 2 years' experience of hands-on laboratory experience, preferably within pharmaceutical, biopharmaceutical, CRO, or CDMO environments.

- Strong experience with HPLC/UHPLC, GC, and core analytical techniques such as dissolution testing, potentiometry, Karl Fischer titration, and UV-Visible spectrophotometry.

- Experience in the development, transfer, qualification, or execution of analytical methods and/or quality control testing.

- Knowledge of GMP requirements and experience working in regulated environments.

- Upper-intermediate (B2) level of English or higher, both written and spoken.

- Ability to interpret analytical results, troubleshoot technical issues, and prepare scientific and technical documentation. xkdbapo

- Availability to work the afternoon shift, from 1:30 PM - 2:00 PM to 9:30 PM - 10:00 PM

Get to Know Kymos

Discover who we are, what we do, and the science that drives our projects.

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