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), and Germany (Frankfurt) and a Liasson 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.
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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 250 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.
We are seeking a highly motivated Scientist to join our Biopharmaceutical Analysis team. This role, reporting to the Department Manager, focuses on the transfer studies of Biological products and validation of Small Molecules products in a GMP-regulated environment.
Key responsibilities:
- Design, supervision and execution of the transfer and validations studies of Biological and Small Molecules Products.
- Hands-on experience with techniques such as chromatography and HPLC.
- Lead and manage assigned projects keeping the deadlines and establishing a direct communication with the client.
- Draft, review, and manage technical documentation associated with the studies (protocols, reports, standard procedures, certificates of analysis,



etc.).
- Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.
Requirements
- Bachelor's or higher degree in Chemistry, Biochemistry, Biotechnology, Pharmacy, or a related life science field.
- Solid hands‑on experience in HPLC methods; Quality Control of Proteins will be a plus.
- In‑depth understanding of GMP requirements.
- Experience with electrophoretic techniques, Western‑Blot and ELISAs will be considered a strong asset.
- Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
- English level equivalent to Cambridge First Certificate (B2) or higher.
- Availability to work in afternoon shifts (1:30 PM- 9:30 PM).
If you join us, you will enjoy:
- Working in a dynamic company with a highly qualified growing team.
- Professional development and collaborative environment and a culture of empowerment.
- Adaptable Working Hours and intensive schedule on Friday.
- Hybrid work, but mainly in the office.
- Access to the employee benefits flexibility platform.
- 23 vacation days per year plus 24th and 31th of December.
- Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
- Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.
Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. xqbhyrx For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.
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📌 Biopharmaceutical Scientist (afternoon shift) (Bellprat)
🏢 Kymos Group
📍 Bellprat