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 200 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.
We are hiring for a Scientist to incorporate to our Elemental Analysis department.
The person Will be assigned the following responsibilities:
Management and execution of ICP-MS and AAS studies that are carried out for Quality Control and Stability Studies of pharmaceutical, veterinary, health and cosmetic products.Management, execution and review of tests by ICP-MS and AAS for development studies, validation and / or method transfers and routine sample analysis.Design, supervision, review and execution of method validation by ICP-MS and AAS.Drafting and review of related documentation (SOP, protocols, guides, reports, etc.
).Direct involvement in all technical aspects related to analytical methods, problem solving, transfer of analytical methods, etc.Management and writing of Incidents, deviations, OOS and CAPAs.Management and organization of the qualification of the teams assigned to the department.Management of studies and results through LIMS system.Contact with the Quality Control and Stability departments of the companyWork under GMP and GLP compliance.We are looking for a candidate with:
University degree: Chemistry or Pharmacy Bachelor's.Some experience in a Quality Control department in the Pharmaceutical industry or Third-Party Analysis Company (CRO).Experience in management, design and performance of physicochemical tests of active ingredients, drugs, cosmetics, ...Experience in working with computerized systems.Experience in working under GMP and GLP standards.Knowledge of pharmacopoeias, guidelines, regulations that apply in the field of GMPs.Advanced English level is a must.Knowledge of the ICH Q3D guideline will be valued.
#J-18808-Ljbffr