Kymos Group
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 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.
Descripción de la oferta
Per il nostro dipartimento di Impurities Identification & Testing siamo alla ricerca di un/una Scientist per garantire il corretto sviluppo dei progetti analitici assegnati, con particolare focus sulle tecniche di spettrometria di massa.
Le responsabilità della posizione includono:
* Progettare, supervisionare ed eseguire il controllo qualità delle materie prime e dei prodotti finiti
* Gestire i progetti assegnati, rispettando le scadenze e stabilendo una comunicazione diretta con i clienti
* Redigere documenti tecnici associati agli studi (protocolli, rapporti, procedure standard, certificati di analisi)
* Dirigere e supervisionare il lavoro sperimentale del personale tecnico
* Eseguire il lavoro in conformità con le Norme di Buona Fabbricazione (GMP)
For our Impurities Identification & Testing department, we are looking for a motivated Scientist to ensure the correct development of assigned analytical projects, with a focus on mass spectrometry techniques.
The responsibilities of the position include:
* Design, supervise, and execute quality control testing of raw materials and finished products
* Manage assigned projects, keeping deadlines and establishing direct communication with clients
* Write technical documents associated with studies (protocols, reports, standard procedures, certificates of analysis)
* Direct and supervise the experimental work of technical staff
* Perform the work in compliance with Good Manufacturing Practices (GMP)
Requisitos
Il/La candidato/a ideale è in possesso dei seguenti requisiti:
* Laurea in Scienze Chimiche o Biochimiche
* 2-3 anni di esperienza in un ruolo simile
* Conoscenza delle tecniche HPLC e GC, con comprensione dei dipartimenti di sviluppo analitico
* Buona conoscenza dello sviluppo di metodi con tecniche di cromatografia liquida accoppiata alla spettrometria di massa
* Esperienza nella gestione dei documenti tecnici associati agli studi (procedure standard, certificati di analisi, deviazioni, OOS, CAPA, ecc.)
* Esperienza di lavoro in ambienti GMP è richiesta
* Esperienza in ruoli simili nell'industria farmaceutica
* Capacità di lavorare in squadra
* Orientamento ai dettagli e capacità di raggiungere obiettivi
The ideal candidate should meet the following requirements:
* Bachelor's degree in chemical or Biochemical Sciences
* 2-3 years of experience in a similar role
* Knowledge of HPLC and GC techniques, with an understanding of analytical development departments
* Good knowledge of method development with liquid chromatography coupled to mass spectrometry techniques
* Experience in managing technical documents associated with studies (standard procedures, certificates of analysis, deviations, OOSs, CAPAs, etc.)
* Experience working in GMP environments is required
* Experience in similar roles in the pharmaceutical industry
* Teamwork skills.
* Detail-oriented and able to achieve objectives