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": "2026-09-24",
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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": "2026-08-24",
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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",
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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",
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    "title": "Sr. Supervisor QA Complaint Approval",
    "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 belongs to the group of Johnson & Johnson Innovative Medicine and manufactures high quality pharmaceutical products, active pharmaceutical ingredients (APIs) and medical devices. Today Cilag AG is one of the largest pharmaceutical manufacturers in Switzerland supplying all the major global markets. The Schaffhausen facility is a strategic launch and growth site for parenteral products, and we have an impressive pipeline of new and innovative products.\nThe Senior Supervisor, Complaint Quality Approver Team is accountable for leading a team of Complaint Quality Approvers responsible for independent, objective review and approval of complaint records. The role provides people leadership, operational oversight, and quality decision support to ensure complaint investigations are complete, scientifically justified, risk-based, and compliant with applicable procedures and regulations. The Senior Supervisor ensures consistent approval practices, timely record progression, appropriate escalation of quality risks, and continuous capability development across the team.\nKEY RESPONSIBILITIES\nThe Senior Supervisor leads the Complaint Quality Approver team and is responsible for assigning, prioritizing, and monitoring work to ensure compliant and timely approval of complaint records. The role provides guidance to approvers on investigation strategy, risk assessment, escalation, evidence requirements, Root Cause Analysis, NC considerations, and alignment of investigation conclusions across products or affiliates when applicable. The Senior Supervisor ensures that approval decisions are made consistently and are supported by objective evidence, applicable procedures, and current regulatory expectations. In addition, the role reviews complex or high-risk complaint records, supports escalation to Quality leadership, and drives alignment with cross-functional partners when investigation direction, closure readiness, or quality risk requires leadership input.\nThe Senior Supervisor is accountable for developing team capability through coaching, feedback, training, and performance management. The role establishes clear expectations for documentation quality, approval rationale, system usage, and stakeholder communication, and ensures the team applies best practices consistently. The Senior Supervisor monitors workload, cycle time, quality metrics, backlog, and recurring investigation trends to identify improvement opportunities, remove barriers, and support sustainable business continuity. The role also contributes to process improvement initiatives, inspection readiness, audit support, and the implementation of global or site quality system changes impacting complaint record approval.\nKEY INTERFACES\nComplaint Quality Approvers to provide leadership, coaching, work prioritization, and performance feedback.\nComplaint investigation owners and cross-functional contributors, including Manufacturing, QC, Engineering, Supply Chain, Packaging, MSAT, Regulatory, and Medical Safety as applicable.\nQuality leadership for escalation, risk communication, resource planning, operational performance, and decision alignment.\nOther sites and affiliates to align investigation strategy, closure expectations, evidence requirements, and consistent complaint outcomes for site-manufactured products.\nAudit, inspection readiness, quality systems, and process improvement stakeholders to support compliant execution and continuous improvement.\nREQUIRED KNOWLEDGE & SKILLS\nStrong knowledge of quality investigations, complaint handling, CAPA and nonconformance concepts in a regulated pharmaceutical or medical product environment.\nDemonstrated ability to lead, coach, and develop a team in a quality organization, including setting priorities and managing performance.\nStrong understanding of cGMP, Good Documentation Practices, data integrity expectations, and applicable U.S. and international regulatory requirements.\nProven ability to assess complex technical data, investigation conclusions, risk assessments, and escalation needs.\nAbility to make sound quality decisions, communicate clear rationale, and ensure consistency in approv",
    "datePosted": "2026-08-04",
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    "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": "2026-08-02",
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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": "2026-07-31",
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    "title": "Supervisor, Quality Control Microbiology",
    "description": "Johnson & Johnson AG is looking for a Supervisor, Quality Control Microbiology to join the team in .\n\n\nAs a Supervisor, Quality Control Microbiology, your key responsibilities will be:\n\n• Within our Quality Control Microbiology department,\n• we are looking for a Supervisor QC Microbiology to join our team\n• . This is an exciting opportunity to contribute to a dynamic, international environment where quality, collaboration, and continuous improvement are at the core of everything we do.\n• About the Role\n• In this role, you will\n\n\nThe ideal candidate profile:\n\n• Formation et expérience en lien avec le poste\n\n• Capacité à travailler en autonomie et en équipe\n\n• Rigueur, ponctualité et sens des responsabilités\n\n\nApply now for this Supervisor, Quality Control Microbiology position in .",
    "datePosted": "2026-07-09",
    "validThrough": "2026-08-08",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/supervisor-quality-control-microbiology-johnson-johnson-ag-ch-finance-banque",
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