AurigaVision AG

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    "title": "Scientist, Validation & Investigations (Ref. 2772) - French speaking | 6 month duration",
    "description": "AurigaVision AG est a la recherche d'un(e) Scientist, Validation & Investigations (Ref. 2772) - French speaking | 6 month duration pour son site de Zug.\n\nOur client is a science-driven pharmaceutical organization focused on developing and ensuring robust manufacturing processes across the full product lifecycle. For a manufacturing site in Switzerland, we are currently looking for a\nScientist, Validation & Investigations (Ref. 2772)\nFrench speaking | 6 month duration\nIn this role you will support validation and investigation activities within manufacturing processes, contributing to product quality and compliance. The position involves close collaboration with cross-functional teams, including Engineering, Technical Services, Manufacturing, Quality Control, and Quality Assurance. In addition, the role requires interaction with global MS&T teams and participation in continuous improvement initiatives.\nYour main tasks\n•\nPrepare and maintain validation and qualification documentation, including protocols, reports, and traceability matrices\n•\nExecute validation, qualification, and robustness activities, including data collection and analysis\n•\nSupport the implementation of new products, technologies, and systems at the manufacturing site\n•\nAssess the impact of changes, deviations, and maintenance interventions on validated systems\n•\nConduct and lead investigations, including root cause analysis and implementation of corrective and preventive actions\n•\nPerform scientific risk assessments and contribute to deviation classification processes\n•\nParticipate in audits, inspections, and continuous improvement activities within MS&T projects\nYour profile\n•\nDegree in Engineering, Chemistry, Pharmacy, or a related natural science field\n•\nFluency in French & English\n•\nProfessional parcours professionnel in pharmaceutical operations, validation, or quality-related functions (MS&T)\n•\nSolid understanding of current regulatory requirements and GxP standards\n•\nStrong analytical and problem-solving skills\n•\nAbility to work across functions and communicate effectively at different organizational levels\n•\nParcours professionnel in health authority inspections or audit support is considered a plus\nDavid Gareis\nis looking forward to receiving your application documents via job portal (CV, diploma, reference letters; no motivational letter necessary).\nFull discretion is guaranteed and we will gladly answer any additional questions.\n\nInteressé(e) ? Postulez directement sur notre site.",
    "datePosted": "2026-06-04",
    "validThrough": "2026-07-04",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/head-of-market-access-ref-2762-zurich-interim-contract-at-least-until-end-of-2026#jobposting",
    "title": "Head of Market Access (Ref. 2762) - Zurich | interim contract at least until end of 2026",
    "description": "Offre d'emploi : Head of Market Access (Ref. 2762) - Zurich | interim contract at least until end of 2026 -- AurigaVision AG, Zug.\n\nOur client is an internationally active, large pharmaceutical company with a strong presence in Switzerland and a global footprint. Located in the greater Zurich area, the organization is known for its innovative focus and its commitment to improving patients’ lives in highly specialized therapeutic areas. On behalf of our client, we are currently looking for a\nHead of Market Access (Ref. 2762)\nZurich | interim contract at least until end of 2026\nIn this position, you will take ownership of complex Market Access and pricing topics in Switzerland and act as a key contributor to strategically relevant submissions and access initiatives. You will work closely with senior internal stakeholders across Commercial, Medical, Regulatory, Finance and Legal functions, as well as represent the organisation in interactions with external bodies. The role involves operating confidently in a highly dynamic and cross-functional environment.\nYour main tasks\n•\nDefine and drive the Market Access and pricing strategy for the Swiss market\n•\nLead and coordinate dossier development, submission and approval processes\n•\nPrepare and conduct negotiations with the Federal Office of Public Health (FOPH/BAG)\n•\nManage complex cross-functional projects involving Commercial, Medical and Regulatory teams\n•\nProvide strategic guidance on reimbursement, pricing and access-related topics\n•\nAnalyse and navigate highly complex questions within the Swiss healthcare system\n•\nAct as a senior internal and external stakeholder and advisor on Market Access matters\nYour profile\n•\nIdeally more than 10 years of experience in Market Access and Pricing & Reimbursement within Switzerland\n•\nProven track record in dossier preparation, submission processes and authority interactions\n•\nSolid negotiation experience with the FOPH/BAG and deep knowledge of the Swiss healthcare landscape\n•\nStrong strategic mindset with the ability to manage complex and ambiguous situations\n•\nDemonstrated leadership parcours professionnel, either in line management or project leadership roles\n•\nHigh level of confidence working in cross-functional and matrix organisations\n•\nFluent in English and German\nDomagoj Odrljin\nis looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no motivational letter necessary).\nFull discretion is guaranteed and we will gladly answer any additional questions.\n\nCe poste est a pourvoir rapidement. Candidatez sans tarder.",
    "datePosted": "2026-05-12",
    "validThrough": "2026-06-11",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/senior-quality-manager-fvp-ref-2760-zurich-immediately-available-interim-assignment-until-end-of-year#jobposting",
    "title": "Senior Quality Manager - FvP (Ref. 2760) - Zurich | Immediately Available | Interim Assignment Until End of Year",
    "description": "Rejoignez AurigaVision AG en tant que Senior Quality Manager - FvP (Ref. 2760) - Zurich | Immediately Available | Interim Assignment Until End of Year a Zug.\n\nOur client is a large, internationally operating pharmaceutical company with a strong footprint in Switzerland and a well-established quality-driven culture within a highly regulated environment. To ensure robust Swiss affiliate coverage and maintain a high level of inspection readiness, we are currently supporting our client in the search for an experienced quality professional who can step in at short notice as\nSenior Quality Manager - FvP (Ref. 2760)\nZurich | Immediately Available | Interim Assignment Until End of Year\nIn this role, you will take ownership of the Swiss affiliate Quality Management System (QMS) and ensure ongoing GDP compliance, effective complaint handling, and sustained inspection readiness. You will work closely with Supply Chain/Distribution, Regulatory Affairs, Pharmacovigilance, and Medical/Commercial stakeholders, and collaborate with regional/global Quality teams as well as external partners such as logistics providers and suppliers.\nYour main tasks\n•\nProvide interim FvP/deputy FvP coverage, including technical supervision of the affiliate QMS and facilities during team absences\n•\nEnsure GDP-compliant import/export and wholesale distribution, including oversight of safe distribution practices\n•\nTake decisions and/or provide oversight for batch release and returns release/rejection in line with internal and external requirements\n•\nOwn and maintain the local QMS, including approval of local quality documents and alignment with global operational documents\n•\nLead quality issue management (change control, deviations, escalations) and coordinate quality defect handling and recall-related activities\n•\nOversee product complaint handling, ensuring timely execution with internal stakeholders and external logistics partners\n•\nDrive inspection readiness and continuous improvement, including support of audits/inspections, self-assessments, training, and proper archiving/records management\nYour Profile\n•\nDegree in Pharmacy, Life Sciences, or a related discipline; strong background in GxP/GDP (GMP is a plus)\n•\nProven experience as FvP or Deputy FvP (Stv. FvP) within a Swiss affiliate or comparable regulated environment\n•\nSolid hands-on knowledge of GDP workflows (e.g., batch release activities, temperature deviations, (mock) recalls, audits/inspections)\n•\nStrong expertise in QMS / Quality Risk Management with an analytical, pragmatic, solution-oriented mindset\n•\nConfident communicator with the ability to collaborate effectively in a cross-functional, matrix organization\n•\nLanguages: German (proficient) and English (business fluent) required\nDomagoj Odrljin\nis looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no motivational letter necessary).\nFull discretion is guaranteed and we will gladly answer any additional questions.\n\nVotre prochaine etape professionnelle commence ici.",
    "datePosted": "2026-05-03",
    "validThrough": "2026-08-01",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/medical-science-liaison-oncology-schweiz-mitte-ref-2754-bs-be-so-ag-zentralschweiz#jobposting",
    "title": "Medical Science Liaison Oncology - Schweiz Mitte (Ref. 2754) - (BS/BE/SO/AG/Zentralschweiz)",
    "description": "Our client is a well‑established, globally active pharmaceutical company with a strong footprint in the Swiss market and a diverse portfolio of innovative therapies across several specialty areas. As part of the expansion of their medical affairs activities in the oncology field, we are supporting their search for a dedicated scientific expert for the Swiss organization. We are therefore looking for a  Medical Science Liaison Oncology - Schweiz Mitte (Ref. 2754) - (BS/BE/SO/AG/Zentralschweiz)   In this role, you will take on a key scientific function and collaborate closely with leading oncology centers and medical experts. You will work in partnership with cross-functional colleagues from Medical Affairs, Marketing, Sales, Regulatory Affairs and Market Access to support scientific exchange and contribute to the medical strategy. The position offers a dynamic environment with strong impact on scientific communication and stakeholder engagement.  Your main tasks   Establish and maintain scientific relationships with key external experts and oncology institutions Provide scientific information and deliver medical training sessions for internal stakeholders Support local medical projects, advisory boards and scientific events Contribute to the development and implementation of regional medical plans and scientific initiatives Collaborate with cross-functional teams to ensure consistent and compliant scientific communication Handle medical information requests and provide accurate, evidence-based responses Ensure compliance with Swiss regulations, internal policies and all relevant industry standards    Your profile   Several years of professional experience in a Medical Science Liaison role (or related) University degree in life sciences, medicine, pharmacy or a related field, with a PhD considered an advantage Fluency in English and German mandatory Strong scientific understanding of oncology and the ability to interpret complex data Excellent communication skills with the ability to present scientific content clearly and engagingly Proven ability to collaborate effectively with healthcare professionals and multidisciplinary teams Structured, proactive and detail-oriented working style with strong compliance awareness Willingness to travel regularly within the assigned region   David Gareis is looking forward to receiving your application documents via job portal (CV, diploma, reference letters; no motivational letter necessary).Full discretion is guaranteed and we will gladly answer any additional questions.",
    "datePosted": "2026-04-01",
    "validThrough": "2026-06-30",
    "employmentType": "FULL_TIME",
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