1 job found in Bern

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    • bern, bern
    • contract
    Do you want to work in a big pharmaceutical company? Do you have experience in CSV? You should then read the following lines! Our client, based in the Bern area, is looking for a CSV Engineer for a 10 months contract. Main ResponsibilitiesSupport closing a CPA regarding audit trail review for QC equipmentCategorize all QC GxP systems according to global SOP and define the frequency of System Audit Trail review based on risk.Perform a System Audit Trail review for those systems that require it based on their categorization.Set up a maintenance task in SAP to plan subsequent reviews Who we are looking forDegree in a LifeSciences/ Biotechnology, Chemistry discipline or comparable work experienceSeveral 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 11, ...)Good understanding of analytical technologies,Strong analytical thinking and problem-solving abilityExcellent communication and teamwork skillsAbility to simultaneously support multiple projects, duties and assignments and prioritize accordinglyExcellent writing skills for scientifically sound technical documents, instructions, protocols and reports.Self-dependent way of working and taking ownership of assigned task to plan and deliver according to agreed timelines.Good verbal and written skills in English, German is a plus Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    Do you want to work in a big pharmaceutical company? Do you have experience in CSV? You should then read the following lines! Our client, based in the Bern area, is looking for a CSV Engineer for a 10 months contract. Main ResponsibilitiesSupport closing a CPA regarding audit trail review for QC equipmentCategorize all QC GxP systems according to global SOP and define the frequency of System Audit Trail review based on risk.Perform a System Audit Trail review for those systems that require it based on their categorization.Set up a maintenance task in SAP to plan subsequent reviews Who we are looking forDegree in a LifeSciences/ Biotechnology, Chemistry discipline or comparable work experienceSeveral 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 11, ...)Good understanding of analytical technologies,Strong analytical thinking and problem-solving abilityExcellent communication and teamwork skillsAbility to simultaneously support multiple projects, duties and assignments and prioritize accordinglyExcellent writing skills for scientifically sound technical documents, instructions, protocols and reports.Self-dependent way of working and taking ownership of assigned task to plan and deliver according to agreed timelines.Good verbal and written skills in English, German is a plus Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.

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