pSelect how often (in days) to receive an alert: /p h3Group Senior Analyst Quality Applications /h3 pJob ID: 64420 /p pLocation: /ppLachen, CH /p pJob Level: Professionals /p pJob Category: IT /p pBecome part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.br/Join us in shaping our vision to provide new health solutions advancing human life. /p h3Your main tasks and responsibilities /h3 ul liActing as subject matter expert for global Quality applications (e.g. Veeva QualityDocs, Veeva QMS, LIMS and related systems), ensuring they remain compliant, user-centric, and fit for purpose. /li liManaging the application lifecycle, including configuration, access models, documentation, validation readiness, and ongoing performance monitoring in a GxP-regulated environment. /li liCollecting, analysing, and structuring business requirements from Corporate Quality, local sites, and Process Owners, translating them into clear solution designs and change requests. /li liCoordinating and supporting system changes and releases, including solution design, testing, validation documentation, and user acceptance testing. /li liServing as escalation point for functional support, incidents, and problem management while ensuring timely resolution with internal IT teams and external vendors. /li liCollaborating closely with Quality, IT, Validation, Architecture, and external partners to enable compliant, efficient, and harmonized Quality processes. /li liDriving continuous improvement and digitalization, proactively proposing enhancements based on system insights, user feedback, and industry best practices. /li liBuilding and maintaining a strong global key-user and site administrator network, including training delivery, communication of roadmaps, and release updates. /li /ul h3Your expertise and ideal skill set /h3 pYou are a proactive professional with a strong "can-do" attitude who enjoys taking ownership and making things happen in a complex, regulated environment. /p pWe are looking for someone with: /p ul liA Bachelor’s degree in IT, Business Informatics, Life Sciences, or a comparable qualification. /li li5–7 years of hands‑on experience working with Quality applications in the pharmaceutical or life‑science industry. /li liStrong practical experience with Quality systems such as Veeva QualityDocs, Veeva QMS, LIMS or equivalent regulated platforms. /li liSolid understanding of GxP requirements, validation principles, and regulated system environments. /li liProven experience in requirements management, change coordination, testing, and validation. /li liStrong analytical and conceptual skills, with the ability to translate business needs into pragmatic system solutions. /li liStructured, detail‑oriented working style combined with excellent communication and stakeholder‑management skills. /li liHigh level of independence, ownership, and initiative, paired with a collaborative and service‑oriented mindset. /li liFluency in English (spoken and written); additional languages are an asset. /li /ul h3Your department - where you make an impact /h3 ul liWe, the Business Applications department, are the trusted partner that drives the digital transformation of Octapharma. Together with Business, we create and deliver digital solutions to transform the organization and improve performance. /li liWe are passionate, flexible and collaborate to create value with fit for purpose solutions for Octapharma. /li /ul h3Thrive with usbr/ /h3 ul liYou help save lives - Every day is meaningful as we produce life‑saving medicines /li liFamily values - Long‑term perspective for employees and relationships /li liBe rewarded with market‑related salary and benefits package /li liYou will have a high level of influence where you can make a difference and leave your footprint /li liWork with skilled and fun colleagues in a relatively informal organization /li liSkills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions /li /ul h3It´s in our blood /h3 pWe live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.br/Please apply in English. /p pDo you have any questions? Then get in touch with your contact person. /p pOctapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care.br/With seven RD sites and five state‑of‑the‑art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 200 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. /p #J-18808-Ljbffr
Group Senior Analyst Quality Applications Arbeitgeber: Octapharma Plasma
Als Arbeitgeber im Bereich Blut- und Plasmaspende bieten wir eine sinnstiftende Tätigkeit, die direkt zur Rettung von Leben beiträgt. Unser Spendezentrum in Cottbus zeichnet sich durch ein engagiertes Team, geregelte Arbeitszeiten ohne Nacht- und Wochenenddienste sowie zahlreiche Benefits wie kostenlose Gesundheitsangebote und ein offenes Betriebsklima aus. Wir fördern die persönliche und berufliche Entwicklung unserer Mitarbeitenden und bieten eine strukturierte Einarbeitung in einem zukunftsorientierten Unternehmen.
