Manager Group Quality System (f/m/d) 80 100% Bachem is a leading, innovation driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. Bachem is a leading, innovation driven company specializing in the development and manufacture of peptides and oligonucleotides. The company, which has over 50 years of experience and expertise, provides products for research, clinical development, and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in the new Group Quality organization, we are looking for a dedicated Manager Group Quality System (f/m/d) 80 100%. Your tasks System administration and higher level system support for Bachems global eQMS system including upgrade/patch management, troubleshooting, communication with the vendor, etc. Ensure cGMP compliance of Bachems global eQMS system and imbedded processes e.g. document and training management, quality event and change management. Offer expert level insights on eQMS processes, serving as a reference point for internal stakeholders. Implementation and documentation of new system configurations, system changes, data migrations, etc. Implementation and harmonization of cGMP eQMS processes across Bachem sites. Execution and documentation of system tests and system validation. Administration, creation and revision of global documents in Bachems global DMS. Lead and/or collaborate in digitalization projects as QA representative. Support of customer audits and authority inspections as SME for Bachems global eQMS system and imbedded processes. Your profile Bachelor Degree or higher qualification in information technologies, life sciences (chemistry, engineering) or similar. At least 5 years experience in Quality System Management in cGMP regulated environments. Thorough knowledge of cGMP regulations related to computerized system validation including CFR 21 Part 11, EU GMP Annex 11 and GAMP standards. Experience in the configuration of database supported software solutions e.g. DMS, QMS, LIMS, ERP. Experience in working in cross functional teams. Ability to communicate in a proactive and solution focused manner. Detail oriented with the