Stability Scientist
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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.
Job description
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 Stability Scientist to join our Stability 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:
- Coordinate and supervise ICH, ongoing, in-use, and photostability studies.
- Manage assigned projects, ensuring timelines, quality standards, and client expectations are met.
- Act as the main scientific contact for clients, maintaining effective communication throughout the project lifecycle.
- Prepare and review study documentation, including protocols, reports, standard operating procedures, and certificates of analysis.
- Supervise and support laboratory staff during the execution of experimental activities.
Requirements
To move forward together, you will need:
- A university degree in Chemistry, Biochemistry, Biotechnology, Pharmacy, or a related scientific discipline.
- Between 3 and 6 years of hands-on laboratory experience, preferably within pharmaceutical, biopharmaceutical, CRO, or CDMO environments.
- Practical experience with HPLC/UHPLC, GC, and core analytical techniques such as dissolution testing, potentiometry, Karl Fischer titration, and UV-Visible spectrophotometry.
- Knowledge of GMP requirements and experience working in regulated environments.
- B2 English and high level of Spanish.
- Strong teamwork and problem-solving skills.
- Ability to organize and manage multiple projects simultaneously.
- Availability to work the afternoon shift, from 1:30 PM – 2:00 PM to 9:30 PM – 10:00 PM.
We will particularly value:
- Experience in the analysis and quality control of proteins, monoclonal antibodies, biosimilars, or other biological products.
- Hands-on experience with techniques such as Capillary Electrophoresis, SDS-PAGE, Western Blot, and ELISA.
What will you find at Kymos?
- Permanent contract.
- Annual training plan and growth opportunities within an expanding company.
- Flexibility in start and finish times, as well as in planning your vacations.
- Flexible compensation plan: private health insurance, transportation, or meal benefits.
- Additional compensation for the afternoon shift.
- Fruit and nuts available to enjoy two days per week.
- Our headquarters are located in Cerdanyola del Vallès, in a green setting at the foothills of Collserola, featuring a rooftop terrace and convenient parking facilities.
Apply now and help advance your potential with Kymos
At Kymos, we consider diversity and inclusion key priorities for our development. One of our main objectives is to promote a culture that values differences and recognizes the unique talent of every individual. Therefore, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion, or any other personal characteristic.
Get to Know Kymos
Discover who we are, what we do, and the science that drives our projects.
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