Ubicación: Barcelona (España)
Tipo de Contrato: Indefinido
Jornada laboral: Jornada completa
Sector: Farmacéutico y biotecnología 
Vacantes: 1
Disciplina: Calidad
Modalidad de trabajo: PresencialKYMOS 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.
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.
Kymos is hiring a Scientist in our Bioanalysis department:
Position Description:
We offer a position in the Bioanalysis Department as a Scientist responsible for the analysis of active ingredients and pharmaceutical specialties.
The Job main missions will be:
The work is conducted in compliance with GLP and GMP regulations.
Education:
Bachelor's degree in Chemical Sciences (Analytical Orientation) with specialization in HPLC-UV.
A Ph.D. is highly valued.
Skills and experience:
Service oriented mindset to deliver on time and with the appropriate level of quality, to research projects expectations/needs.
High experience in HPLC-UV techniques and basic knowledge of LC-MS/MS methods.
Anticipate issues and proactively identify workaround options, showing strong “results” orientation.
Work closely and interact constantly with technicians and clients.
Fluent in speaking, reading and writing professional English.
3/4 years’ experience as Senior Scientist in a pharmaceutical environment and under GLP/GMP regulations.
If you join us, you will become part of an agile and growing company with a strong scientific culture.
Here's what you can expect:
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. 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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