Qa Scientist For Batch Release

The QA Scientist will be assigned the following responsibilities: - Be involved in the revision of manufacturing batch records and packaging batch records and other batch review documents of pharmaceutical products to be released. - Participate in the certification process of batches susceptible to be released to the market or for clinical trials. - Review...

.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...

.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...

.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...

.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...

.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...

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...

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...

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...

NJ Pharma consultng s.r.o. is looking QA person responsible for Batch Release in Barcelona, around 85 hours per month (3 days a week). The person will be responsible for trainings and activities related to batch release. The project would be on freelance basis with independent agreement.

NJ Pharma Consulting s.r.o. is a leading pharmaceutical consulting company seeking an experienced QA professional to lead batch release activities in our Barcelona-based project.This is a freelance opportunity with flexible working hours, ideal for those looking for a part-time commitment. The selected candidate will be responsible for training and related...

.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...

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...

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany, as well as a Liaison 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,...

We are hiring a Quality Assurance Scientist for our GMP area of the Quality Assurance Department. The QA Scientist will be assigned the following responsibilities:Review and approve the documentation involved in the analytical activity of the company: CoA, protocols, reports, SOPs, product specifications.Audit the analytical documentation issued by the...

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany, as well as a Liaison 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,...

Kymos Group, a dynamic and fast-growing Contract Research Organization (CRO), is seeking a highly skilled Senior Pharmaceutical Quality Assurance Specialist to join our team in Spain. As a trusted partner to the life sciences industry, we offer comprehensive bioanalytical and CMC analytical services with GMP and GLP certified laboratories and GCP...

At Kymos Group, we are a medium-sized and rapidly growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Italy and Germany. Our team is dedicated to providing high-quality bioanalytical and CMC analytical services to the life sciences industry. Our laboratories are GMP certified, GLP compliant, and have been successfully...

Responsible for ensuring the GMP- and regulatory conform production of medicinal drugs acc. to guidelines e.g. EU-GMP-Guideline - Review the technical content of SOPs for manufacturing and Quality Control. - Supports the GMP conform process optimization in manufacturing and Quality Control. - Quality review of batch documentation for release purposes -...

**QA Release & Compliance Officer**:Dentro del área de QA Inyectables y Orales, reportando directamente al Responsable de Release & Compliance, el QA Release&Compliance officer I&O será responsable de realizar las siguientes tareas.**Tareas y responsabilidades**:- Recopilar, organizar y completar la documentación establecida para cada lote fabricado en...