Johnson & Johnson AG

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    "title": "Sr. Project Manager Construction Pharma Environment",
    "description": "At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at\njnj.com\n.\nAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.\nCilag AG in Schaffhausen, Switzerland is part of the Johnson & Johnson Innovative Medicine (J&J IM) Supply Chain organization and is currently recruiting for a\nSenior Project Manager Construction Pharma\nThe Senior Project Manager serves as a senior technical leader on capital projects, ensuring alignment to J&J standards and regulatory requirements. This role leads large capital projects, partnering with Quality, EHS, Operations, and external A&E/CM firms.\nKey Responsibilities\nStrategic Project Leadership & Delivery\nLead large capital projects across all project phases (planning, design, procurement, construction, commissioning).\nCoordinate multi-functional engineering strategies to meet schedule, budget, quality, and regulatory requirements.\nTechnical Authority & Governance\nAct as the senior technical authority, review and approve engineering design changes, and technical submittals.\nEnsure engineering solutions align with J&J standards, industry codes, and regulatory expectations.\nBudget & Cost Management\nLead multi‑million‑dollar capital budgets for assigned projects, monitor costs, and support procurement and contractor selection and evaluation.\nParticipate in contractor bid reviews and support value-engineering decisions.\nScheduling, Risk & Performance Management\nLead schedule development and integration with program timelines; identify critical path items and drive mitigation.\nMaintain a proactive risk register, recommend mitigations, and track performance metrics.\nConstruction Management & Field Leadership\nProvide senior owner-side engineering oversight during construction and commissioning; ensure contractor performance aligns with design intent and J&J EHS standards.\nPromote a strong safety culture and ensure EHS compliance on site.\nDocumentation & Reporting\nMaintain detailed engineering records, design documentation, and as-built information.\nPrepare and present executive-level status updates, technical summaries, and risk briefings.\nEducation & Experience\nBachelor’s degree in Engineering, Architecture, or Construction Management required; Master’s degree preferred.\n10+ years of experience leading capital projects, preferably in regulated industries (pharmaceutical, biotechnology, medical device, or similar).\nDemonstrated owner-side engineering leadership and experience working with A&E and Construction Management firms.\nExperience leading multi-discipline teams and collaborating with quality, EHS, operations, and external consultants.\nSkills & Competencies\nStrong technical judgment and problem-solving skills.\nExcellent communication and leadership skills for multi-functional and executive interactions.\nProven track record to lead budgets, schedules, and complex contractor relationships.\nFamiliarity with regulatory expectations for facilities in regulated industries.\nProficiency with project management and engineering documentation tools.\nAdditional Requirements\nLocation of Role:\nPrimary Location: Schaffhausen, Switzerland\nLanguage Requirements:\nProficiency: English & German\nTravel Requirements:\nThis position will require limited travel (less than 10%) domestic and international travel",
    "datePosted": "2026-08-25",
    "validThrough": "2026-11-25",
    "employmentType": "FULL_TIME",
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    "title": "Manager Technical Product Management",
    "description": "Manager Technical Product Management\nWe are seeking an experienced Manger who can evolve our Pharmacovigilance (PV) technology landscape, with a strong focus on case processing systems and operational excellence.\nThis role will partner closely with Safety, Regulatory, and IT teams to drive innovation, scale, and compliance across global PV platforms. The ideal candidate brings deep expertise in ICSR case processing workflows and hands-on experience with ArisGlobal LifeSphere MultiVigilance (LSMV), ReporterX, XDI, and RxLogix (RxL).\nKey Responsibilities\nOwn and execute the product roadmap for Pharmacovigilance (PV) case processing and safety platforms, translating business needs into scalable, compliant technology solutionsLead Agile delivery by prioritizing backlog and driving end-to-end product lifecycle, including design, validation, and releasesOversee end-to-end ICSR case processing capabilities (intake through regulatory submission), ensuring efficiency, quality, and complianceServe as product/IT lead for ArisGlobal LSMV, and manage ReporterX and XDI for intelligent data intake and integration (E2B, structured and unstructured sources)Enable seamless integration with RxLogix (RxL) to support signal detection, reporting, and analyticsDrive adoption of automation and AI to reduce manual effort, improve data quality, and enhance throughputEnsure compliance with global PV regulations (FDA, EMA, ICH E2B, GVP) and maintain audit/inspection readinessMonitor system performance, SLAs, and data quality KPIs; lead issue resolution, risk mitigation, and continuous improvement initiativesAct as primary interface between IT and Pharmacovigilance business teams, aligning on priorities and delivery plansPartner with vendors (e.g., ArisGlobal, RxLogix) on product strategy, upgrades, and innovationOptimize cost, vendor performance, and system utilizationLead and develop a high-performing team, driving performance management, coaching, and a culture of accountability and continuous improvement\nRequired Qualifications\nBachelor’s degree in Information Technology, Life Sciences, or related field5–8+ years of experience in product management or IT application ownership in PharmacovigilanceHands-on experience with:ArisGlobal LifeSphere MultiVigilance (LSMV)ReporterX and XDI (data intake/integration frameworks)RxLogix (RxL) platform (signal detection/reporting/analytics)Strong understanding of ICSR case processing lifecycle and PV compliance requirementsExperience working in GxP-regulated environmentsExposure to Agile methodologies and modern technologies (AI/automation/data platforms)Excellent communication, leadership, and stakeholder management skills\nPreferred Qualifications\nExperience leading global PV platform transformations or migrationsFamiliarity with regulatory inspections and audit supportKnowledge of emerging technologies in AI-driven case processing and signal detection",
    "datePosted": "2026-08-24",
    "validThrough": "2026-11-24",
    "employmentType": "FULL_TIME",
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    "@id": "https://ch-jobs.com/job/local-quality-owner-1#jobposting",
    "title": "Local Quality Owner",
    "description": "At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at\njnj.com\n.\nAs guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.\nCilag AG in Schaffhausen, Switzerland is part of the Johnson & Johnson Innovative Medicine (J&J IM) Supply Chain organization and is currently recruiting for a\nLocal Quality Owner Late Stage & Value Optimizer (f/m/d), 80-100%\nWe manufacture high quality pharmaceutical drug products (Small and Large Molecules) and active pharmaceutical ingredients (APIs). Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all major global markets. The Schaffhausen facility is a center for launching and accelerating growth in parenterals, supported by an impressive pipeline of new and innovative products.\nPosition summary\nThe function holder is responsible for the QA oversight of a selected Portfolio of established (Combination-) Products, which are manufactured at the J&J IM Schaffhausen site.\nPrincipal responsibilities\nKey Contact for internal and external stakeholders (operations, planning, logistics, engineering, regulatory affairs etc.) within cross-functional teams in terms of Quality and Compliance.\nQ&C contributions including Decision making and problem solving and oversight of assigned, established manufacturing lines.\nInvestigation lead for major non-conformances (deviations) including CAPA alignment with Operations counterparts.\nIn-time release of parenteral products (intermediate and finished products).\nProactive risk mitigation.\nReview and approval of non-conformances (deviations) records and change requests.\nReview and approval of GMP critical SAP master data (e. g. bill of material, manufacturing instructions etc.).\nReview and approval of work instructions and standard operating procedures.\nSupport of cross-functional and global projects.\nReview of Annual Product Reviews.\nQualifications\nA minimum of a Bachelor’s degree, preferably in a technical/scientific field. A Master’s degree or advanced is desirable.\nMinimum of 5 years of experience in a GMP regulated Pharma production environment or in a relevant quality or supply chain role.\nStrong understanding of parenteral fill/finish manufacturing incl. device assembly and packaging processes.\nIn-depth knowledge in GMP standards, policies and procedures\nKnowledge about regulatory guidelines preferred\nAdvanced communication skills, verbal and written in both English and German\nWe are looking for a dynamic and solution-oriented individual eager to contribute to our team and drive success in a collaborative, international and fast-paced environment. If you see yourself in this role, we encourage you to share your application materials with us without hesitation.",
    "datePosted": "2026-08-24",
    "validThrough": "2026-11-24",
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    "title": "Manager Technical Product Management",
    "description": "Manager Technical Product Management\nWe are seeking an experienced Manger who can evolve our Pharmacovigilance (PV) technology landscape, with a strong focus on case processing systems and operational excellence.\nThis role will partner closely with Safety, Regulatory, and IT teams to drive innovation, scale, and compliance across global PV platforms. The ideal candidate brings deep expertise in ICSR case processing workflows and hands-on experience with ArisGlobal LifeSphere MultiVigilance (LSMV), ReporterX, XDI, and RxLogix (RxL).\nKey Responsibilities\nOwn and execute the product roadmap for Pharmacovigilance (PV) case processing and safety platforms, translating business needs into scalable, compliant technology solutionsLead Agile delivery by prioritizing backlog and driving end-to-end product lifecycle, including design, validation, and releasesOversee end-to-end ICSR case processing capabilities (intake through regulatory submission), ensuring efficiency, quality, and complianceServe as product/IT lead for ArisGlobal LSMV, and manage ReporterX and XDI for intelligent data intake and integration (E2B, structured and unstructured sources)Enable seamless integration with RxLogix (RxL) to support signal detection, reporting, and analyticsDrive adoption of automation and AI to reduce manual effort, improve data quality, and enhance throughputEnsure compliance with global PV regulations (FDA, EMA, ICH E2B, GVP) and maintain audit/inspection readinessMonitor system performance, SLAs, and data quality KPIs; lead issue resolution, risk mitigation, and continuous improvement initiativesAct as primary interface between IT and Pharmacovigilance business teams, aligning on priorities and delivery plansPartner with vendors (e.g., ArisGlobal, RxLogix) on product strategy, upgrades, and innovationOptimize cost, vendor performance, and system utilizationLead and develop a high-performing team, driving performance management, coaching, and a culture of accountability and continuous improvement\nRequired Qualifications\nBachelor’s degree in Information Technology, Life Sciences, or related field5–8+ years of experience in product management or IT application ownership in PharmacovigilanceHands-on experience with:ArisGlobal LifeSphere MultiVigilance (LSMV)ReporterX and XDI (data intake/integration frameworks)RxLogix (RxL) platform (signal detection/reporting/analytics)Strong understanding of ICSR case processing lifecycle and PV compliance requirementsExperience working in GxP-regulated environmentsExposure to Agile methodologies and modern technologies (AI/automation/data platforms)Excellent communication, leadership, and stakeholder management skills\nPreferred Qualifications\nExperience leading global PV platform transformations or migrationsFamiliarity with regulatory inspections and audit supportKnowledge of emerging technologies in AI-driven case processing and signal detection",
    "datePosted": "2026-08-09",
    "validThrough": "2026-11-09",
    "employmentType": "FULL_TIME",
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