Bioanalysis Scientist

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: R&D
Work modality: On site

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), 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.

Job description

We are hiring a Scientist specialized in HPLC-MS/MS bioanalytical methods to set-up and compound quantification in biological matrices.

The Job main missions will be:

Design, develop and Supervise LC-MS/MS bioanalytical methods for compound determination in biological matrices (sample preparation, method set-up).
Develop and validate new analytical methods with HPLC-MS/MS
Ensure coordination and good performance of laboratory technicians.
Manage the projects directly with our clients.

Requirements

Education:

Degree in analytical chemistry with specialization in Mass Spectrometry

Skills and experience:

Knowledge in analysis of samples, development and analytical validations by HPLC-MS/MS
Knowledge in sample analysis, development and analytical validations by LC-MS / MS will be valued.
Knowledge of GLP regulations will be valued.
Service oriented mindset to deliver, on time and with the appropriate level of quality, to research projects expectations/needs.
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.
1 year experience as Scientist in a pharmaceutical environment.

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: R&D
Work modality: On site

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