nemensis ag

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    "title": "Production Operator - Biotech Manufacturing (m/f/d)",
    "description": "Nouvelle opportunite : Production Operator - Biotech Manufacturing (m/f/d) chez nemensis ag (Luzern, Schachen).\n\nProduction Operator – Biotech Manufacturing (m/f/d)\nReady to Make a Real Impact in Cutting-Edge Biotech Production?\n•\n?\nDuration:\n01.06.2026 – 31.05.2027\n•\n?\nLocation:\nLucerne, Switzerland (Onsite)\n•\n?\nEmployment Type:\nTemporary\nAbout Our Client\nOur client is a renowned biopharmaceutical research and development site based in Central Switzerland, specialising in the biotechnological manufacturing of active substances for clinical use in humans. As part of a globally leading life sciences group, the site plays a pivotal role in the development and supply of innovative medicines including breakthrough oncology treatments and stands for the highest standards in GMP-compliant biotech production.\nYour Responsibilities\n•\nCarry out\nGMP- and GDocP-compliant operations\nin the Weigh & Dispense (W&D) and Solution Supply areas\n•\nExecute\nsampling tasks\nin line with approved sampling plans, SOPs, and batch records\n•\nActively support\nupstream (USP) and downstream (DSP) manufacturing\nprocesses\n•\nAssemble and disassemble\nsingle-use systems\nand process equipment; assist with line clearance and equipment setup\n•\nConduct and support\nwasher and autoclave activities\nin accordance with validated procedures\n•\nPerform\nmaterial staging, transfers, inspections, and inventory checks\n•\nAccurately maintain\nGMP documentation\nincluding batch records, logbooks, and electronic systems\n•\nIdentify, escalate, and document\ndeviations, safety observations, and non-conformities\n•\nAssist with\naudits, inspections, and internal walkthroughs\nas required\nYour Profile\n•\nCompleted\ntechnical or scientific vocational training\n(e.g., Biotechnology, Chemistry, Laboratory Technician or equivalent)\n•\nAt least\n3 years of hands-on GMP manufacturing experience\n, ideally in the biotech or pharmaceutical sector\n•\nSolid knowledge of\nGDP principles and ALCOA+\nstandards\n•\nPractical experience with\ncleanroom environments\nand biotech equipment (single-use and stainless steel systems)\n•\nProven track record in\nsampling, material handling, and GMP documentation\n•\nStrong\nattention to detail\nand a compliance-driven mindset\n•\nProficient in both\nGerman and English\n(written and spoken)\nWhy nemensis?\n•\nNemensis AG is your specialised recruitment partner in the Life Sciences sector, headquartered in Basel.\n•\nComprehensive guidance and support throughout the entire application process by our experienced Consultants.\n•\nAccess to an extensive client network and exciting positions across Northwestern Switzerland.\n•\nFast and straightforward entry through individual coaching and personalised support during the application process.\nApply Now\nAt nemensis ag, we have successfully connected thousands of candidates with their ideal roles opening doors to new career chapters and professional growth. As a\nProduction Operator (m/f/d)\nin\nLucerne\n, this could be your next big step. What can we do for your career today? Get in touch we look forward to hearing from you!\n?\nPhill Rogers\n, Consultant\nWrite an email\nYou're looking for a change, but this role isn't quite the right fit? Register with us anyway we'll reach out to get to know you, understand your goals, and match you with the right opportunity.\n\nRejoignez nemensis ag et donnez un nouvel elan a votre carriere.",
    "datePosted": "2026-06-01",
    "validThrough": "2026-07-01",
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    "title": "Senior Regulatory Affairs Manager - Global Labeling (m/f/d) 100%",
    "description": "nemensis ag ouvre un poste de Senior Regulatory Affairs Manager - Global Labeling (m/f/d) 100% a Basel-Stadt, Basel.\n\nSenior Global Labeling Manager (m/w/d) – Pharmaceutical Regulatory Affairs\nShape the Future of Global Drug Labeling – Your Expertise Matters!\n•\nDuration:\n5 months\n•\nLocation:\nBasel\n•\nEmployment Type:\nTemporary Assignment\n•\nState:\nASAP\nAbout Our Client\nFor our client, a renowned pharmaceutical enterprise in the Basel region, we are seeking an experienced Senior Global Labeling Manager (m/w/d). This innovative organization operates at the forefront of drug development and regulatory excellence, committed to delivering transformative therapies to patients across international markets. With a strong focus on scientific advancement and regulatory compliance, the company plays a leading role in shaping global healthcare standards.\nYour Responsibilities\n•\nAct as the\nprimary point of contact\nfor all labeling-related matters and drive labeling excellence across assigned product portfolios\n•\nDevelop, update, and maintain\nregulatory-compliant global labeling documents\n, including Core Data Sheets (CDS), Basic Patient Leaflets (BPL), and Basic Succinct Statements (BSS)\n•\nLead\nExpert Labeling Task Forces (ELTF)\nto establish labeling strategies, facilitate cross-functional alignment, and achieve consensus on labeling content\n•\nServe as a\ncore member\nof Regulatory Affairs Sub-teams and Safety Management Teams (SMTs) for designated projects and products\n•\nConduct in-depth research on labeling topics by analyzing international labels, competitor documentation, clinical study data, and regulatory frameworks\n•\nPrepare\nhigh-quality regulatory submissions\nsupporting CDS modifications and responses to Health Authority inquiries\n•\nCollaborate with Country Organizations to ensure\ntimely and consistent implementation\nof global labeling updates in local product information\n•\nSupport Regulatory Affairs activities related to\nsafety risk communications\nand portfolio stewardship initiatives with labeling implications\n•\nPresent labeling strategies and updates to relevant boards, forums, and committees (e.g., MSRB, PSB)\n•\nPrepare and review\nPeriodic Safety Update Report (PSUR)\nregulatory input for assigned products\n•\nReview and approve\nInternational Package Leaflets\nto ensure regulatory compliance and quality standards\n•\nProvide\nmentorship and guidance\nto junior team members and new Global Labeling Managers\n•\nContribute to\ncontinuous improvement initiatives\nwithin global labeling management processes\n•\nEvaluate and provide input on emerging\ninternal and external regulatory guidelines\naffecting labeling practices\n•\nRepresent the Global Labeling function during\naudits and regulatory inspections\nYour Profile\n•\nAcademic background:\nBachelor's or Master's degree in life sciences; advanced degree (MD, PhD, PharmD) is highly desirable\n•\nProfessional parcours professionnel:\nSeveral years of direct, hands-on Global Labeling experience in the pharmaceutical industry (ideally 4–6+ years) with clear CDS/CCDS ownership (lead author) and labeling change management responsibility\n•\nFluent in English\nas business language; additional language skills are advantageous\n•\nStrong\ninterpersonal and communication skills\nwith the ability to influence and negotiate effectively\n•\nProven ability to\nlead cross-functional teams\nand manage projects in a matrix organization\n•\nExcellent\norganizational awareness\nand understanding of business priorities and departmental interdependencies\n•\nSolid knowledge of\nmedical and scientific terminology\nand drug safety information\n•\nDemonstrated\nproblem-solving capabilities\nand strategic thinking skills\nWhat We Offer – Your Benefits with nemensis AG\n•\nnemensis AG\nis your specialized personnel partner in the Life Sciences sector, based in Basel\n•\nComprehensive\nconsultation and support\nthroughout the entire application process by our experienced Consultants\n•\nAccess to an\nextensive client network\nand exciting opportunities in Northwestern Switzerland\n•\nQuick and straightforward onboarding\nthrough individual guidance and personalized support during the recruitment process\nReady for Your Next Career Move?\nAt nemensis AG, we've already connected thousands of professionals with their dream jobs, giving them the opportunity to develop further or re-enter the job market. What can we do for you and your career today?\nGet in touch with us!\n?\nPhill Rogers\n, Consultant,\nE-Mail schreiben\nYou're looking for a change of perspective, but this isn't the right position for you? Then register with us – we'll contact you for an initial meeting to understand your wishes and needs and align ourselves accordingly.\n\nSaisissez cette opportunite et postulez des aujourd'hui.",
    "datePosted": "2026-05-11",
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    "title": "QC Bioanalytical Scientist (m/f/d)",
    "description": "Offre d'emploi : QC Bioanalytical Scientist (m/f/d) -- nemensis ag, Luzern, Schachen.\n\nQC Bioanalytical Scientist (m/f/d)\nWhere Science Meets Precision Shape the Future of Biologics Quality Control\n•\n?\nDuration:\n1 year (temporary assignment)\n•\n?\nLocation:\nLucerne/Schachen, Switzerland\n•\n?\nEmployment Type:\nTemporary\nAbout Our Client\nOur client is a globally recognised pharmaceutical organisation with a strong presence in Central Switzerland, operating at the forefront of biologics manufacturing and quality assurance. With a highly regulated GMP environment and a culture driven by scientific excellence, the company sets industry standards in the development, release, and stability testing of biological drug substances.\nAs a\nQC Bioanalytical Scientist (m/f/d)\n, you will take on the following key responsibilities:\n•\nExecution of analytical testing\nfor drug substance release, stability, and characterisation of biologics in compliance with cGMP/GDP regulations\n•\nApplication and operation of specialised analytical techniques\n, including capillary electrophoresis, isoelectric focusing, and protein concentration determination\n•\nSupport of analytical method validation and transfer processes\n, including the preparation of technical protocols and reports\n•\nAccurate documentation\nof all laboratory activities in an electronic laboratory notebook in accordance with cGMP standards\n•\nTroubleshooting of analytical methods\nto ensure seamless qualification and reliable execution in the laboratory\n•\nParticipation in equipment maintenance\n, calibration, and qualification activities as well as periodic reviews\n•\nAdherence to all applicable internal regulations\n, including safety, health, and environmental protection guidelines\nYour Profile\n•\nEducational background\nin laboratory sciences: qualification as a laboratory technician (EFZ), or a Bachelor's or Master's degree in a relevant scientific discipline\n•\nPractical experience\nwith capillary electrophoresis (e.g. Sciex PA800 Plus), isoelectric focusing (e.g. Maurice, BioTechne), and UV-based protein concentration determination\n•\nProficiency in chromatography data systems\nused for electrophoresis methods, such as Empower\n•\nSolid cGMP working parcours professionnel\nin a regulated pharmaceutical or biotechnology environment\n•\nStrong communication skills\nin both English and German (minimum B1–B2 level in both languages)\n•\nAbility to collaborate effectively\nin cross-functional, team-oriented settings\n•\nKnowledge of\nprotein biochemistry\nand/or biophysical analytical methods is an advantage\nAt nemensis ag, we have successfully connected thousands of candidates with their ideal positions, supporting them in advancing their careers or re-entering the job market. We would be pleased to discuss how we can support\nyour\nprofessional journey as a\nQC Bioanalytical Scientist (m/f/d)\nin\nLucerne/Schachen\n. We look forward to receiving your application.\n?\nPhill Rogers, Consultant,\nWrite an email\nYou are looking for a new professional direction, but this particular role is not the right fit? Register with us we will reach out to schedule an introductory conversation to understand your goals and preferences, and align our services accordingly.\n\nRejoignez nemensis ag et donnez un nouvel elan a votre carriere.",
    "datePosted": "2026-05-04",
    "validThrough": "2026-06-03",
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    "title": "Clinical Packaging Technician (m/w/d) 100%",
    "description": "   Packaging Technician Clinical Studies (m/w/d)    Ihre Chance in der pharmazeutischen Verpackungstechnologie!     Dauer: 2 Jahre  Einsatzort: Schachen LU  Vermittlungsart: Temporär    Über unseren Kunden   Für unseren Kunden, ein führendes biopharmazeutisches Unternehmen mit Schwerpunkt auf Forschung und Entwicklung im Bereich klinischer Studien, suchen wir einen engagierten Packaging Technician Clinical Studies (m/w/d). Das Unternehmen zählt zu den innovativen Akteuren der pharmazeutischen Industrie in der Zentralschweiz und setzt höchste Qualitätsstandards in der GMP-konformen Produktion und Verpackung von Prüfpräparaten.   Ihre Aufgaben     Verpackungsoperationen: Durchführung von manuellen und halbautomatischen Abfüll-, Etikettierungs- und Verpackungsprozessen für Studienmedikamente (Tabletten, Kapseln) unter strikter Einhaltung der GMP-Richtlinien  Maschinenbedienung: Steuerung und Überwachung von Verpackungsanlagen und technischen Geräten zur Herstellung von klinischem Studienmaterial  Präzise Dokumentation: Führung von Logbüchern, elektronischen Batch-Dokumentationen sowie verpackungsspezifischen Aufzeichnungen gemäss internen Qualitätsvorgaben  SAP-Administration: Durchführung von SAP-Transaktionen und Sicherstellung der korrekten Systemnutzung im Verpackungsbereich  SOP-konforme Arbeitsweise: Exakte Umsetzung von Standard Operating Procedures, Batch-Vorschriften und Verpackungsanweisungen  Qualitätssicherung: Unverzügliche Meldung von Abweichungen oder besonderen Vorkommnissen an die verantwortlichen Studienleitenden    Ihr Profil     Teamfähigkeit: Ausgeprägte Fähigkeit zur Zusammenarbeit in interdisziplinären Teams  Präzision und Struktur: Hohe Genauigkeit und methodisches Vorgehen bei der täglichen Arbeit  Technisches Verständnis: Affinität für den Umgang mit technischen Geräten und Maschinen  Sprachkenntnisse: Fliessende Deutschkenntnisse; Englischkenntnisse sind von Vorteil  IT-Kompetenzen: Sicherer Umgang mit MS-Office-Anwendungen und SAP-Systemen  GMP-Bewusstsein: Bereitschaft zur strikten Einhaltung pharmazeutischer Qualitätsstandards    Vorteile Nemensis    Nemensis AG ist Ihr spezialisierter Personalvermittler im Bereich Life Sciences mit Sitz in Basel Umfassende Beratung und Betreuung im Bewerbungsprozess durch unsere Consultants Zugang zu einem grossen Kundennetzwerk und spannenden Stellen in der Nordwestschweiz Schneller und unkomplizierter Einstieg durch individuelle Begleitung und Beratung im Bewerbungsprozess    Bereit für den nächsten Karriereschritt?   Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Was können wir heute für Sie und Ihre Karriere tun? Bewerben Sie sich jetzt für die Position als Packaging Technician Clinical Studies (m/w/d) in Schachen LU und werden Sie Teil eines innovativen pharmazeutischen Umfelds!   Kontakt   ? Phill Rogers, Consultant,  Sie streben einen Perspektivenwechsel an, aber das ist nicht die richtige Stelle für Sie? Dann registrieren Sie sich bei uns – wir kontaktieren Sie für ein Kennenlerngespräch, um Ihre Wünsche und Bedürfnisse abzuholen und uns danach auszurichten.   ",
    "datePosted": "2026-04-04",
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    "@id": "https://ch-jobs.com/job/elektroingenieur-m-w-d-100#jobposting",
    "title": "Elektroingenieur (m/w/d) 100%",
    "description": "  Elektrotechniker / Elektroingenieur Electrical Engineering (m/w/d)   Gestalte die elektrotechnische Zukunft – in einem der innovativsten Unternehmen der Life Sciences!    ? Eintritt: Ab sofort ? Einsatzort: Raum Basel ? Homeoffice: Nach Vereinbarung    Über unseren Kunden   Für unseren Kunden, ein international tätiges und technologieführendes Unternehmen im Bereich Reinraumtechnologie und Isolatortechnik für die pharmazeutische Industrie, suchen wir eine engagierte Fachperson im Electrical Engineering. Mit über 1'600 Mitarbeitenden und einem weltweiten Marktanteil von 20–25 % bei hochwertigen Isolatoren zählt das Unternehmen zu den angesehensten Partnern globaler Pharmakonzerne und Forschungslaboratorien – mit Hauptsitz in der Nordwestschweiz.   Deine Aufgaben    Projektverantwortung für Standardisierungsvorhaben im Electrical Engineering – inklusive Kosten-, Termin-, Ressourcen- und Qualitätssteuerung  Auswahl, Pflege und Weiterentwicklung elektrotechnischer sowie pneumatischer Komponenten und Systeme  Erstellung und Pflege von Vorgabedokumenten, Prozessbeschreibungen und Vorlagen für den Fachbereich  Aktive Mitwirkung in fach- und standortübergreifenden Arbeitsgruppen sowie Development- und Product-Care-Projekten  Schulung und Wissenstransfer zu eingesetzten Systemen und Komponenten (inkl. Datenpflege)  Koordination mit Lieferanten sowie fachtechnische Unterstützung interner Stakeholder    Dein Profil    Abgeschlossene Ausbildung als Elektrotechniker HF oder Elektroingenieur FH  Mehrjährige Berufserfahrung als Projektierungsingenieur oder Projektleiter in einem vergleichbaren Umfeld Fundierte Kenntnisse in EPlan sowie in der Arbeit mit DMS-Systemen  Mehrjährige Erfahrung im Umgang mit Tools wie Excel VBA oder ähnlichen Systemen Kenntnisse in der Pneumatik von Vorteil Strukturierte, eigenverantwortliche Arbeitsweise mit ausgeprägter Kommunikationsstärke  Sehr gute Deutschkenntnisse sowie gutes technisches Englisch     Das bietet dir die nemensis ag   Bei der nemensis ag haben wir bereits tausende Bewerberinnen und Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder neu in den Arbeitsmarkt einzusteigen. Als Elektrotechniker / Elektroingenieur Electrical Engineering (m/w/d) im Raum Basel wartet eine spannende Herausforderung auf dich – wir begleiten dich auf dem Weg dorthin.  Was können wir heute für dich und deine Karriere tun? Melde dich bei uns!   ? Phill Rogers, Consultant,     Du strebst einen Perspektivenwechsel an, aber das ist nicht die richtige Stelle für dich? Dann registriere dich bei uns – wir kontaktieren dich für ein Kennenlerngespräch, um deine Wünsche und Bedürfnisse abzuholen und uns danach auszurichten.   ",
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