Group Senior Analyst Quality Applications

Octapharma recherche un Analyste Senior Qualité à Lachen. Une opportunité de contribuer à des projets impactants et à un environnement de travail collaboratif.TâchesAgir en tant qu'expert sur les applications Qualité mondiales.Gérer le cycle de vie des applications, y compris la validation.Analyser et structurer les exigences des utilisateurs pour les solutions.CompétencesDiplôme en IT, 5-7 ans d'expérience en systèmes qualité.Expérience avec des systèmes comme Veeva QualityDocs et LIMS.Compétences analytiques et en gestion des exigences.Group Senior Analyst Quality ApplicationsJob ID: 61472Location:Lachen, CHJob Level: ProfessionalsJob Category: ITEmployment Type: Permanent positionCareer Level:Become 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.Join us in shaping our vision to provide new health solutions advancing human life.Your main tasks and responsibilitiesActing assubject matter expertfor global Quality applications (e.g. Veeva QualityDocs, Veeva QMS, LIMS and related systems), ensuring they remain compliant, user‑centric, and fit for purpose.Managing theapplication lifecycle, including configuration, access models, documentation, validation readiness, and ongoing performance monitoring in a GxP‑regulated environment.Collecting, analysing, and structuringbusiness requirementsfrom Corporate Quality, local sites, and Process Owners, translating them into clear solution designs and change requests.Coordinating and supportingsystem changes and releases, including solution design, testing, validation documentation, and user acceptance testing.Serving asescalation point for functional support,incidents, and problem management while ensuring timely resolution with internal IT teams and external vendors.Collaborating closelywith Quality, IT, Validation, Architecture, and external partners to enable compliant, efficient, and harmonised Quality processes.Drivingcontinuous improvement and digitalisation, proactively proposing enhancements based on system insights, user feedback, and industry best practices.Building and maintaining a strongglobal key‑user and site administrator network,including training delivery, communication of roadmaps, and release updates.Your expertise and ideal skill setYou are a proactive professional with a strong "can‑do" attitude who enjoys taking ownership and making things happen in a complex, regulated environment.We are looking for someone with:A Bachelor’s degree in IT, Business Informatics, Life Sciences, or a comparable qualification.5–7 years of hands‑on experience working with Quality applications in the pharmaceutical or life‑science industry.Strong practical experience with Quality systems such as Veeva QualityDocs, Veeva QMS, LIMS or equivalent regulated platforms.Solid understanding of GxP requirements, validation principles, and regulated system environments.Proven experience in requirements management, change coordination, testing, and validation.Strong analytical and conceptual skills, with the ability to translate business needs into pragmatic system solutions.A structured, detail‑oriented working style combined with excellent communication and stakeholder‑management skills.High level of independence, ownership, and initiative, paired with a collaborative and service‑oriented mindset.Fluency in English (spoken and written); additional languages are an asset.Your department - where you make an impactWe, 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 organisation and improve performance.We are passionate, flexible and collaborate to create value with fit for purpose solutions for Octapharma.Thrive with usYou help save lives - Every day is meaningful as we produce life-saving medicinesFamily values - Long-term perspective for employees and relationshipsBe rewarded with market-related salary and benefits packageYou will have a high level of influence where you can make a difference and leave your footprintWork with skilled and fun colleagues in a relatively informal organizationSkills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutionsIt´s in our bloodWe 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.Please apply in English.Do you have any questions? Then get in touch with your contact person.Mrs. Claudia VignauOctapharma AGSeidenstrasse 2, 8853 LachenT: +41 55 451 21 35Want to find out more about us?Visit our websiteOctapharma Careerand follow us daily onLinkedIn.About OctapharmaOctapharma 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. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.