Engineering Project Manager for CSL Behring in Bern

ppWe make it GmbH is a company operating nationally in Switzerland. Thanks to many years of successful experience, it has a high level of competence in the personnel services sector. Concentration of placement activities on the core areas of industry, technology, office/administration, engineering, pharmaceuticals and IT. We make itbr/GmbH places the highest demands on quality, ethics and discretion. /p pFor our customer, the company CSL Behring, we are searching for: /p pbEngineering Project Manager /b /p pbDescription /b /p pCSL Behring AG in Bern specializes in the manufacture of drugs for the treatment of immune deficiencies and immune dysfunction, as well as drugs for rhesus prophylaxis and albumin solutions for shock and burn victims. CSL Behring AG's production facilities are licensed by the Swiss health authorities and the US FDA. Every year, therapeutically important proteins are isolated from over six million liters of human plasma in accordance with the strictest safety and quality standards and processed into medicines. The products of CSL Behring AG are distributed worldwide. /p pCSL Behring is a leading global biotherapeutics company committed to its promise to save lives. The parent company, CSL Limited, is headquartered in Melbourne, Australia. /p pbWorking hours /b /p pStandard / 41 working hours /p h3Aufgaben /h3 ul liResponsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands /li liLeads multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements /li liDevelops and maintains integrated project plans and monitors project activities for adherence to milestone timelines, deliverables and budget against approved plan /li liMaintain oversight on project risks and develops risk mitigation strategies /li liEnsures that initiatives are aligned with the business objectives and strategic philosophy /li liResponsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval /li liResponsible for implementing EHS by design principles in the project /li liResponsible for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for site Sr. Management and Global Steering Committees /li liProject Teams are responsible for completion of project lifecycle activities through performance qualification /li liInfluences teams to work collaboratively, to be customer focused and to deliver superior performance through personal leadership abilities, mentoring and effective communication /li /ul h3Qualifikation /h3 ul liSuccessful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent) /li li10 years of experience in managing capital projects in the pharmaceutical industry /li liIdeally experience of Annex 1 and filling lines /li liFunctional knowledge of cGMPs and manufacturing operations in FDA regulated facility /li liExcellent understanding of project management principles and project lifecycle phases, including knowledge of Validation, CMC and facility regulatory submission requirements /li liExperience to manage high level project budgets /li liAbility to handle many tasks simultaneously and integrate project planning efforts across functions /li liAbility to understand “the big picture” and approach problem solving in a proactive team manner /li liGerman is mandatory /li liExperience in Execution system /li liExperience in Trackwise /li liExperience in Veeva /li liPower BI/Clarity. /li /ul pbAre you interested? /b /p pThen Mr. Raphael Sigg looks forward to receiving your complete /p papplication documents (CV, certificates and training certificates). We look forward to hearing from you. /p /p #J-18808-Ljbffr