Bioanalysis Scientist

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany, and a Liasson office in South Korea, 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 to providing high quality and added value services to its partners and is highly oriented to innovation, offering services in 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 200 employees and is committed to promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

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

The main responsibilities 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-UV.
• Ensure coordination and good performance of laboratory technicians.
• Manage projects directly with our clients.

Requirements

Education:

• Degree in analytical chemistry with specialization in Mass Spectrometry.
• Skills in compound quantification by LC-MS/MS.

Skills and experience:

• Knowledge in analysis of samples by HPLC-UV.
• Knowledge in development and analytical validations by HPLC-UV.
• Knowledge of sample analysis by LC-MS/MS will be valued.
• Knowledge in development and analytical validations by LC-MS/MS will be valued.
• Knowledge of in vitro percutaneous absorption tests 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 project expectations/needs.
• Anticipate issues and proactively identify workaround options, showing strong results orientation.
• Work closely and interact constantly with technicians and clients.
• Fluency in speaking, reading, and writing professional English.
• 1 year of experience as a Scientist in a pharmaceutical environment and under GLP regulations.
• Knowledge of in vitro percutaneous absorption tests will be a plus.