70 opportunita di lavoro per glp in Italia aggiornate oggi
offerte di lavoro trovate
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Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Un'azienda farmaceutica globale cerca un tirocinante per supportare la revisione della documentazione relativa alla Qualità e Compliance. Il candidato ideale ha una laurea in discipline scientifiche e interesse per il settore. Le responsabilità includono la revisione QA della documentazione e la col
Un'azienda farmaceutica globale cerca un tirocinante per supportare la revisione della documentazione relativa alla Qualità e Compliance. Il candidato ideale ha una laurea in discipline scientifiche e interesse per il settore. Le responsabilità includono la revisione QA della documentazione e la col
OverviewAdvarra Consulting seeks independent GxP auditors with experience in clinical research, quality assurance, and related life sciences to perform independent audits across GxP domains (GCP, GCLP, GLP, GMP, GVP, CSV).ResponsibilitiesAuditor Engagements (may include any of the following)CRO Audi
AdvarraOverview Advarra Consulting seeks independent GxP auditors with experience in clinical research, quality assurance, and related life sciences to perform independent audits across GxP domains (GCP, GCLP, GLP, GMP, GVP, CSV). Responsibilities Auditor Engagements (may include any of the following) CRO
AdvarraOverview Advarra Consulting seeks independent GxP auditors with experience in clinical research, quality assurance, and related life sciences to perform independent audits across GxP domains (GCP, GCLP, GLP, GMP, GVP, CSV). Responsibilities Auditor Engagements (may include any of the following) CRO
Un'azienda farmaceutica globale cerca un tirocinante per supportare la revisione della documentazione relativa alla Qualità e Compliance. Il candidato ideale ha una laurea in discipline scientifiche e interesse per il settore. Le responsabilità includono la revisione QA della documentazione e la col
AdvarraOverview Advarra Consulting seeks independent GxP auditors with experience in clinical research, quality assurance, and related life sciences to perform independent audits across GxP domains (GCP, GCLP, GLP, GMP, GVP, CSV). Responsibilities Auditor Engagements (may include any of the following) CRO
Biotecnologie - Farmacia - ChimicaA leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
San Raffaele Telethon Institute For Gene Therapy (Sr-Tiget)Un istituto di ricerca biomedica cerca un Computer System Validation Specialist Junior per unirsi al team QA. Di seguito, troverà un'analisi completa di tutti i requisiti per i potenziali candidati e le istruzioni su come candidarsi. In bocca al lupo! Il ruolo include la preparazione della documenta
Kedrion BiopharmaUn'azienda farmaceutica globale cerca un tirocinante per supportare la revisione della documentazione relativa alla Qualità e Compliance. Il candidato ideale ha una laurea in discipline scientifiche e interesse per il settore. Le responsabilità includono la revisione QA della documentazione e la col
Un istituto di ricerca biomedica cerca un Computer System Validation Specialist Junior per unirsi al team QA. Il ruolo include la preparazione della documentazione di validazione e la collaborazione nella valutazione della convalida delle apparecchiature. Si richiede una Laurea in Biologia o Biotecn
Biotecnologie - Farmacia - ChimicaA leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
Pharmaprogress S.r.L.A leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's d
Biotecnologie - Farmacia - ChimicaA leading Contract Research Organization in Ancona seeks a Finished Products Testing Scientist. The role involves managing quality control testing, writing technical documents, and supervising technical staff while maintaining compliance with GLP and GMP standards. Candidates need a Bachelor's degre
18.000 € – 29.000 €all'anno
Affidabilita della stima: Bassa
Stima basata sui dati di mercato. Gli stipendi effettivi possono variare in base a esperienza, azienda e localita.
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