16.05.24 | Vollzeit | Bern | Randstad Schweiz AGknowledge and experience in GMP quality systems. - Aware of maintenance management, compliance, GMP and other regulatory standards. - Excellent oral and written communication
Später ansehen16.05.24 | Vollzeit | Bern | Randstad Schweiz AGManagement/execution on electrical topics - Previous experience working in the Pharmaceutical industry - Thorough knowledge of GMP & GxP regulations in Switzerland as well normas and technical standards for the electrical installations - Fluency in German and English - Availability to work 100% at site
Später ansehen16.05.24 | Vollzeit | Bern | Randstad Schweiz AGYour Profile - Degree in a LifeSciences/ Biotechnology, Chemistry discipline or comparable work experience - Several years of experience in computerized system validation (CSV) in a GMP environment and good knowledge of related regulatory requirements in the life sciences industry (GAMP 5, 21 CFR part
Später ansehen14.05.24 | Vollzeit | Bern | Randstad Schweiz AGSteps such as chromatography; UF/DF - Experience in Upstream is a plus - Excellent problem solving and analytical capabilities - Knowledge in Statistic - Team player and a personality with
Später ansehen07.05.24 | Vollzeit | Bern | Randstad Schweiz AGOr Master's degree in Engineering or a related field. - Minimum of 5 years of experience in commissioning and qualification activities in in pharmaceuticals or biotechnology industry. - Strong knowledge and understanding of GMP (Good Manufacturing Practice) guidelines and regulatory requirements. - Experience
Später ansehen07.05.24 | Vollzeit | Bern | Randstad Schweiz AGAnd oversight of external suppliers Your Profile - Bachelor’s or Master’s degree in Engineering or a related field. - Minimum of 3 years of experience in commissioning and qualification activities in in pharmaceuticals or biotechnology industry. - Strong knowledge and understanding of GMP (Good Manufacturing
Später ansehen25.04.24 | Vollzeit | Bern | Randstad Schweiz AGAnd procedures are managed effectively. Requirements - Bachelor's or master's degree in technical or natural sciences. - Minimum 3 years of working experience within pharma or biotech. - Minimum 4 years of working experience with CSV. - Knowledge of FDA 21CFR part 11/EUGMP Annex 11 regulations and ISPE GAMP 5
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