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:
* 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 #J-18808-Ljbffr

📌 Quality Control Scientist (Cataluña)
🏢 Kymos Group
📍 Cataluña