Technicien Buffer FormulationNous sommes à la recherche d'un Technician Buffer Formulation (m/f/d) pour une durée de 12 mois. Au sein du département Biotech (Global Health care Organization), intégrez avec votre savoir-faire l'équipe du Buffer Formulation DSP à la production BP, une équipe performante de techniciens, spécialisés dans la préparation de tampons pour la production de protéines recombinantes produites à partir de cellules animales. En tant qu
Technicien Buffer FormulationNous sommes à la recherche d'un Technician Buffer Formulation (m/f/d) pour une durée de 12 mois. Au sein du département Biotech (Global Health care Organization), intégrez avec votre savoir-faire l'équipe du Buffer Formulation DSP à la production BP, une équipe performante de techniciens, spécialisés dans la préparation de tampons pour la production de protéines recombinantes produites à partir de cellules animales. En tant qu
We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
As part of the Global Drug Substance Development department, you will join a team of motivated scientists dedicated to develop and optimize process for production of new biological therapeutics.As a member of the Downstream Purification team, you will participate to the establishment of a new purification process for a Biologic entity by ensuring the robustness and efficiency of this process. You will be responsible for the technical operation on robotized
As part of the Global Drug Substance Development department, you will join a team of motivated scientists dedicated to develop and optimize process for production of new biological therapeutics.As a member of the Downstream Purification team, you will participate to the establishment of a new purification process for a Biologic entity by ensuring the robustness and efficiency of this process. You will be responsible for the technical operation on robotized
Nous sommes à la recherche d'un USP/DSP Compliance (m/f/d) pour une durée de 12 mois.Rejoignez notre équipe dynamique au sein d'un environnement de production stimulant, où vous jouerez un rôle clé dans le suivi des activités de compliance pour les processus Upstream (USP) et Downstream (DSP). En étroite collaboration avec les différentes équipes du site, vous serez responsable de la gestion de la documentation, de la signalisation et du traitement des ano
Nous sommes à la recherche d'un USP/DSP Compliance (m/f/d) pour une durée de 12 mois.Rejoignez notre équipe dynamique au sein d'un environnement de production stimulant, où vous jouerez un rôle clé dans le suivi des activités de compliance pour les processus Upstream (USP) et Downstream (DSP). En étroite collaboration avec les différentes équipes du site, vous serez responsable de la gestion de la documentation, de la signalisation et du traitement des ano
Reportingto the 'Analytical Development& Innovation Lab Manager'in the Global Analytical Development organization, this role represents anopportunity to significantly contribute to the high-tech analyticallaboratories in the BDC, by conducting analytical testing, data evaluation and reporting, toensure the delivery of our specialty innovator Biotech pipeline to patients. Your Role:Conduct routine analytical testing in at least one of the following area
Reportingto the 'Analytical Development& Innovation Lab Manager'in the Global Analytical Development organization, this role represents anopportunity to significantly contribute to the high-tech analyticallaboratories in the BDC, by conducting analytical testing, data evaluation and reporting, toensure the delivery of our specialty innovator Biotech pipeline to patients. Your Role:Conduct routine analytical testing in at least one of the following area
We are seeking a highly organized and detail-oriented Packaging Artwork Coordinator and Reviewer to join our team. This role is pivotal in ensuring the smooth development and review of packaging artwork for our biopharma and Medical Device products. The successful candidate will coordinate artwork modifications, ensuring compliance with regulatory standards while maintaining high-quality output. Key Accountabilities:Support and coordinate all packaging dev
We are seeking a highly organized and detail-oriented Packaging Artwork Coordinator and Reviewer to join our team. This role is pivotal in ensuring the smooth development and review of packaging artwork for our biopharma and Medical Device products. The successful candidate will coordinate artwork modifications, ensuring compliance with regulatory standards while maintaining high-quality output. Key Accountabilities:Support and coordinate all packaging dev
Your role : Reporting to the 'Analytical Operations & Quality Control Microbiology Lab Manager' in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to the startup of high-tech GMP analytical laboratories, by actively participating to QC microbiological processes set up, and be responsible to: Perform Bacterial Endotoxin Testing (BET), Bioburden, and Low Bioburden testing on various samplesRevie
Your role : Reporting to the 'Analytical Operations & Quality Control Microbiology Lab Manager' in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to the startup of high-tech GMP analytical laboratories, by actively participating to QC microbiological processes set up, and be responsible to: Perform Bacterial Endotoxin Testing (BET), Bioburden, and Low Bioburden testing on various samplesRevie
Reporting to Analytical Development Lab Manager in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to the startup of high-tech analytical laboratories, by supporting the development and implementation of automated high throughout analytical assay to support therapeutics proteins process development.Your key responsibilities in this role are:Contribute to the development of new end to end robot
Reporting to Analytical Development Lab Manager in the Global Analytical Development organization, this role represents an opportunity to significantly contribute to the startup of high-tech analytical laboratories, by supporting the development and implementation of automated high throughout analytical assay to support therapeutics proteins process development.Your key responsibilities in this role are:Contribute to the development of new end to end robot
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