Kymos Group

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés- Barcelona), Italy (Monsano-Ancona), Germany (Frankfurt), Denmark (Copenhagen) and a Liaison office in South Korea (Seoul), offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA.

KYMOS GROUP is devoted in providing high quality and added value services to its partners and it is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies.

KYMOS GROUP has a young and dynamic staff of more than 330 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

Descripción de la oferta

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 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:

- 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

To move forward together, you will need:

- 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.

- 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.

https://www.youtube.com/watch?v=DdhXQimMS20

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