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    14 Jobs für Compliance in Vaud gefunden

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      • Corsier-sur-vevey, Vaud
      • Temporär
      Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég
      Au sein du département Engineering & Maintenance, vous intégrerez l'équipe E&M Compliance & Qualification en tant que compliance. L'équipe, performante et dynamique, assure la compliance GMP au sein du département E&M.Vos Tâches :En tant que compliance, vous aurez principalement la charge de la gestion des déviations du départementVous avez la charge de la mise en place d'actions de corrections et de prévention efficacesVous serez point de contact privilég
      • Vevey, Vaud
      • Temporär
      Pour le département Data & Digital , nous recherchons un " Compliance Engineer " sur le site Merck à Corsier sur Vevey :Mission :Participation au suivi des items Qualité de l’équipe Data & Digital tel que la rédaction des investigations de déviations, des actions correctives et préventives (CAPA), ainsi que les actions de CCP liés aux systèmes automatisés/informatisésExécution et suivi des revues périodiques des systèmesVotre profil :Bachelor, Master, Ingé
      Pour le département Data & Digital , nous recherchons un " Compliance Engineer " sur le site Merck à Corsier sur Vevey :Mission :Participation au suivi des items Qualité de l’équipe Data & Digital tel que la rédaction des investigations de déviations, des actions correctives et préventives (CAPA), ainsi que les actions de CCP liés aux systèmes automatisés/informatisésExécution et suivi des revues périodiques des systèmesVotre profil :Bachelor, Master, Ingé
      • Corsier-sur-vevey, Vaud
      • Temporär
      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
      • Aubonne, Vaud
      • Temporär
      Nous recherchons pour notre client Merck un.e Compliance Production Specialist, pour une mission d'une durée de 12 mois. Vos Missions: Assurer la gestion des déviations, CAPA, Change Control liés à l'activité aseptique.Prend en charge la rédaction de l'ensemble de la documentation liée aux activités aseptiques.Prend en charge les observations en chambre liées au comportement aseptique des opérateurs de production.Support production de l'ensemble du départe
      Nous recherchons pour notre client Merck un.e Compliance Production Specialist, pour une mission d'une durée de 12 mois. Vos Missions: Assurer la gestion des déviations, CAPA, Change Control liés à l'activité aseptique.Prend en charge la rédaction de l'ensemble de la documentation liée aux activités aseptiques.Prend en charge les observations en chambre liées au comportement aseptique des opérateurs de production.Support production de l'ensemble du départe
      • Aubonne, Vaud
      • Temporär
      Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
      Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
      • Corsier-sur-vevey, Vaud
      • Temporär
      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
      • Corsier Sur Vevey, Vaud
      • Temporär
      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
      • Aubonne, Vaud
      • Temporär
      The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure the
      The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure the
      • Aubonne, Vaud
      • Temporär
      The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be r
      The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be r
      • Aubonne, Vaud
      • Temporär
      Ton rôleEn tant que Technicien QC Support, tu joueras un rôle clé dans le soutien des activités de contrôle qualité au sein de l'équipe. Tu seras amené à participer aux activités d'échantillonnage de matières et de produits, du maintien des zones de travail classées, et de la laverie centralisée du contrôle Qualité, tout en garantissant le respect des bonnes pratiques de fabrication (GMP) et des standards qualité de Merck.Réaliser l'échantillonnage des mat
      Ton rôleEn tant que Technicien QC Support, tu joueras un rôle clé dans le soutien des activités de contrôle qualité au sein de l'équipe. Tu seras amené à participer aux activités d'échantillonnage de matières et de produits, du maintien des zones de travail classées, et de la laverie centralisée du contrôle Qualité, tout en garantissant le respect des bonnes pratiques de fabrication (GMP) et des standards qualité de Merck.Réaliser l'échantillonnage des mat
      • Aubonne, Vaud
      • Temporär
      Take the opportunity to be a key protagonist in Quality Control (QC) for Biopharmaceuticals on a growing site in a mutating environment. By joining us you will be part of a site which delivers outstanding solutions to patients for more than 30 years. Contribute to this exciting and challenging journey within the QC Support and Technology team by supporting crucial activities related to the QC laboratory new equipment implementation.Your role : In link wit
      Take the opportunity to be a key protagonist in Quality Control (QC) for Biopharmaceuticals on a growing site in a mutating environment. By joining us you will be part of a site which delivers outstanding solutions to patients for more than 30 years. Contribute to this exciting and challenging journey within the QC Support and Technology team by supporting crucial activities related to the QC laboratory new equipment implementation.Your role : In link wit
      • Corsier-sur-vevey, Vaud
      • Temporär
      An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan
      An exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan
      • Montreux, Vaud
      • Festanstellung
      Job Title: PsychotherapistLocation: Montreux, SwitzerlandJob Type: Full-Time / Part-TimeSalary: Competitive, based on experience About the Role:We are seeking an experienced and dedicated Psychotherapist to join our clients team in Switzerland. The successful candidate will work with individuals, couples, and families to address a wide range of psychological challenges, offering therapeutic interventions, and supporting clients in improving their mental he
      Job Title: PsychotherapistLocation: Montreux, SwitzerlandJob Type: Full-Time / Part-TimeSalary: Competitive, based on experience About the Role:We are seeking an experienced and dedicated Psychotherapist to join our clients team in Switzerland. The successful candidate will work with individuals, couples, and families to address a wide range of psychological challenges, offering therapeutic interventions, and supporting clients in improving their mental he
      • Eysins, Vaud
      • Temporär
      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

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