PKYMOS 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. /ppKYMOS 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. /ppKYMOS 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. /ppFor ourstrongImpurities Identification Testing department /strong, we are looking for a motivatedstrongScientist /strongtoensure the correct development of assigned analytical projects, with a focus on strongmass spectrometry /strong strongtechniques. /strong /ppstrongThe responsibilities of the position include: /strong /pulliDesign, supervise, and execute quality control testing of raw materials and finished products /liliManage assigned projects, keeping deadlines and establishing direct communication with clients /liliWrite technical documents associated with studies (protocols, reports, standard procedures, certificates of analysis) /liliDirect and supervise the experimental work of technical staff /liliPerform the work in compliance with Good Manufacturing Practices (GMP) /li /ulpstrongThe ideal candidate should meet the following requirements: /strong /pulliBachelor’s degree in chemical or Biochemical Sciences /lili2-3 years of experience in a similar role /liliKnowledge of HPLC and GC techniques, with an understanding of analytical development departments /liliGood knowledge of method development with liquid chromatography coupled to mass spectrometry techniques /liliExperience in managing technical documents associated with studies (standard procedures, certificates of analysis, deviations, OOSs, CAPAs, etc.) /liliExperience working in GMP environments is required /liliExperience in similar roles in the pharmaceutical industry /liliDetail-oriented and able to achieve objectives /li /ul #J-18808-Ljbffr