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Bavarian Nordic Berna GmbH

📍 Bern (BE)
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💼 Offerte di lavoro 10

Global Category Manager, CAPEX & Engineering Services (f/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Switzerland

Bavarian Nordic Berna GmbH est a la recherche d'un(e) Global Category Manager, CAPEX & Engineering Services (f/m/d) pour son site de Switzerland. At Bavarian N…

Achats / Approvisionnement Chimie / Pharma Switzerland
Pubblicato il 26 Jun 2026 👁 2 visualizzazioni
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    "description": "Bavarian Nordic Berna GmbH est a la recherche d'un(e) Global Category Manager, CAPEX & Engineering Services (f/m/d) pour son site de Switzerland.\n\nAt Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial product portfolio includes market-leading vaccines against smallpox, mpox, rabies, tick-borne encephalitis, typhoid fever, and cholera. We excel in R&D innovation, manufacturing, and commercialization, striving to improve people's health and quality of life worldwide, protecting our tomorrow.\nAs Global Category Manager for CAPEX & Engineering Services (f/m/d), you will partner with global and site engineering stakeholders to define and execute the end-to-end category strategy for capital investments and engineering services across the network. You will ensure the timely, cost-effective, and risk-controlled delivery of CAPEX projects and services, driving value through supplier strategy, contracting, and complex negotiations. You will build and manage a strong global supplier base, foster collaboration with key stakeholders, and leverage deep market expertise to translate insights into measurable outcomes, including cost optimization, improved project execution, and reduced projects delivery risk.\nThis hybrid position, located in either Kvistgaard, Denmark; or Bern, Switzerland requires travel to other Bavarian Nordic locations as needed 15-20% and reports to the Head of Global Procurement.\nKey responsibilities\n•\nDevelop and maintain category strategies and plans for CAPEX & Engineering Services, identifying opportunities to drive value through cost optimization, risk mitigation, safety, innovation, and improved capital project execution\n•\nOwn end-to-end category management responsibilities, ensuring effective governance, execution, and performance\n•\nAnalyze procurement data and market intelligence to identify savings opportunities, process efficiencies, and performance improvements\n•\nDesign and implement innovative sourcing and contracting solutions that deliver measurable cost savings and operational improvements\n•\nManage strategic supplier relationships, resolving key issues and ensuring high performance in delivery, quality, and compliance\n•\nLead contractual and commercial governance with suppliers to support strategic priorities and ensure value protection over the lifecycle of agreements\n•\nSupport procurement transformation and change initiatives to improve category performance and business outcomes\n•\nMaintain deep expertise in global CAPEX and engineering services markets, including supplier landscape, cost drivers, and innovation trends\nSkills and Experience\n•\nBachelor's degree in engineering, Finance, Business, or a related field; MBA preferred\n•\nProfessional procurement certification (e.g., CIPS) preferred\n•\n7+ years of experience in procurement or strategic sourcing roles with CAPEX or Engineering services category or project responsibility\n•\nProven experience managing procurement for large-scale CAPEX and engineering projects, including delivery of strategic sourcing initiatives and measurable business value\nWhy join us?\nThis role sits within our Global Procurement organization and offers the opportunity to directly shape and enable large-scale capital investment projects that support company growth and operational capability. Leveraging your experience, you will play a key role in driving value creation, risk management, and execution excellence across global CAPEX and engineering spend. In this position, you will also have the mandate to influence global procurement practices and strengthen category management standards, contributing to a more strategic, consistent, and high-performing procurement organization within Bavarian Nordic.\nReady to make a Difference?\nPlease submit your CV as soon as possible; We are interviewing on an ongoing basis and look forward to receiving your motivated CV. A cover letter is not required.\nAs we are approaching the summer period, you may parcours professionnel a longer recruitment timeline than usual due to holidays.\nWe kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and\nNorth America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bavarian-nordic.com\nBavarian Nordic\n\nInteressé(e",
    "datePosted": "2026-06-26",
    "validThrough": "2026-07-26",
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Head of Medical Safety GCSP

🕑 Part-time 🏢 In sede 📍 Bern

Poste a pourvoir : Head of Medical Safety GCSP -- Bern -- Bavarian Nordic Berna GmbH. At Bavarian Nordic, we are committed to saving and improving lives by unl…

Bern Chimie / Pharma Gestion / Management Qualité
Pubblicato il 05 Jun 2026 👁 8 visualizzazioni
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    "description": "Poste a pourvoir : Head of Medical Safety GCSP -- Bern -- Bavarian Nordic Berna GmbH.\n\nAt Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial portfolio includes market-leading vaccines against smallpox/mpox, rabies, tick-borne encephalitis, typhoid fever, and cholera. We excel in R&D innovation, manufacturing, and commercialization-working every day to protect people's health and quality of life and protecting our tomorrow.\nWe are looking for an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP).\nThe position reports to the Head GCSP & EU/UK QPPV and can be based in either Germany or Switzerland - travel up to ~20% within Europe should be expected.\nThe role\nAs our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. In this role, you will manage and mentor a team of six (Sr) Safety Physicians and (Sr) Safety Scientists.\nKey responsibilities\n•\nLead and develop the medical safety team and ensure that appropriate tools and skillsets are available/developed\n•\nEnsure high quality clinical safety contributions to development programs and for the life-cycle management of marketed products in compliance with regulations, guidelines, BN operating procedures (SOPs)\n•\nServe as member of the GCSP Leadership Team and in governance committees as assigned\n•\nEnsure medical safety support for GCP and GVP audits and inspections\n•\nContribute to company strategic initiatives and innovations\n•\nStay abreast of innovative technologies, tools, innovations, and regulations concerning area of expertise\nWhat you bring\nTo become a success in this role, you bring a Medical Doctor (MD) degree combined with leadership experience within clinical safety and pharmacovigilance. You are recognized for setting direction, taking accountability, and leading teams with passion, clarity and empathy in a highly regulated, global environment. You balance strategic oversight with confident decision?making and strong ethical stakeholder engagement.\n•\n10+ years of parcours professionnel across clinical safety and pharmacovigilance, including senior Medical Safety roles\n•\nDeep regulatory expertise across global safety activities, including signal management and risk minimization\nYou bring solid knowledge of global clinical safety and pharmacovigilance regulations including GCP, GVP, and ICH guidelines, along with hands-on experience in CTD compilation and MAAs/BLAs submissions to major health authorities. Besides this, you communicate fluently in English with solid written, verbal, and presentation skills using medical and regulatory terminology. You are highly proficient in relevant IT tools and database applications and are a self-driven, positive team player who helps to build and sustain high performance and team cohesion.\nMost importantly, you thrive in change; your judgment, integrity, and resilience help safeguard patient safety and support our transition from development to full commercialization in a fast-moving, life-science environment. Please note an advanced degree is required, and an MD qualification is mandatory for this role.\nWhy this role\nThis role offers a unique opportunity to take end?to?end responsibility for all medical safety activities within clinical safety and pharmacovigilance in a science driven organization with a strong purpose. You will mentor a team, work closely with global stakeholders, contribute directly to regulatory submissions and patient safety, and have real influence on how safety processes and risk management activities are shaped and executed. It is a role with both strategic impact and hands?on responsibility, ideal, if you want to grow your expertise while making a meaningful difference.\nIn this role, you will have the platform to make a lasting impact on public health, advance our mission, and set new benchmarks for medical excellence in a dynamic, growth-oriented biotechnology environment.\nApplication\nIf you are ready to take on a pivotal role in a growing organization and drive meaningful change in healthcare, apply now and join Bavarian Nordic in our mission to improve health outcomes and foster sustainable growth.\nPlease note that we do not support any relocation package for this role.\nWe kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America",
    "datePosted": "2026-06-05",
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Senior Computer System Validation Engineer (f/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Rejoignez Bavarian Nordic Berna GmbH en tant que Senior Computer System Validation Engineer (f/m/d) a Bern. For us, it is all about improving and saving lives …

Bern Chimie / Pharma Construction d'installations / d'appareils
Pubblicato il 04 Jun 2026 👁 21 visualizzazioni
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    "title": "Senior Computer System Validation Engineer (f/m/d)",
    "description": "Rejoignez Bavarian Nordic Berna GmbH en tant que Senior Computer System Validation Engineer (f/m/d) a Bern.\n\nFor us, it is all about improving and saving lives\nIn Bern, we're not just expanding-we'reexpanding-we're reaching a major milestone by launching a new production site and introducing innovative ways of working. This is what being a Persistent Pioneer in our BNBN DNA is all about-bringingabout-bringing a pioneering spirit to everything we do. Whether you're an experienced professional, transitioning from academia, or coming from a related industry, you'll have the unique opportunity to influence how we work and grow.\nWe are looking to strengthen the Engineering Team with a\nSenior Computer System Validation Engineer (f/m/d)\n- Parental cover for 12 months -\nOur engineering department is a close-knit team of more than 30 employees that covers all engineering aspects in-house. We operate like a family, supporting each other, and are composed of regional and international specialists. Our team communicates in both German and English. Continuous development is in our DNA, as is the goal to achieve something extraordinary.\nMain responsibilities\n•\nReview and approve CSVCSV and OT-related system lifecyclelifecycle design documentation (user requirements, functional and design specifications, data flow diagrams, commissioning, and qualification protocols)\n•\nPerforms cycle driven tasks including ComputerizedComputerized System Periodic Review, Data Integrity Assessment and Risk/Gap assessments and mitigation activities\n•\nCommissioning and qualification of software, spreadsheets and computerizedcomputerized equipment\n•\nDeviation Investigation, Change Control and CAPACAPA Management: Lead Projects, site changes and Risk Management activities related to CSV\n•\nCSVProvides customer focus supporting engineering, research and development, quality, manufacturing sciences and technology, and manufacturing as a Subject Matter Expert for CSV tCSVopics\nYour Educational Background and professional expertise\n•\nBS/MSc iMScn IT, Computer Science or equivalent with a strong track record in Biotech-Industry\n•\nProfessional Expertise: Minimum of 5 years of experience in CSV rCSVelated field, with project management experience\n•\nLanguages: English, oral and written, German is a plus\nExpected technical competencies\n•\nTechnical / Lifecycle DLifecycleocumentation: Creation/execution of CSV dCSVeliverable packages including URS, URSFDS, FDSHDS, HDSCommissioning, Qualification Protocols/Reports, data flow diagrams, Periodic Review Reports, Data Integrity Assessment and Risk/GAP Assessment Reports\n•\nSystem Validation: commissioning and qualification of software, spreadsheets and computerized ecomputerizedquipment/systems\n•\nProject Management: Demonstrate ability to lead and manage CSV aCSVnd OT projects, ensuring coordination with stakeholders and adherence to timelines and budgets\n•\nRegulatory Knowledge: Comprehensive understanding of GMP, GMPFDA, GAMP5 aGAMP5nd other relevant regulatory guidelines\n•\nAudit participation expertise\nWe provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and professional skills.\nAre you ready to join us in our mission?\nIf this sounds like the next step in your career, we would love to hear from you. Simply click the \"APPLY\" button on the right side of the page and you will be redirected to our application form. We are conducting interviews on an ongoing basis and encourage you to apply as soon as possible.\nWe look forward to receiving your motivated CV, where you briefly explain your motivation for applying for this particular position. A cover letter is optional.\nApplications submitted via email will not be considered.\nWe kindly request that headhunters or recuitment arecuitmentgencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a fonction to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox ampoxnd smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, colorsex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bwwwavarian-nbavarianordic.cnordicom\nBavarian Nordic\n\nN'attendez pas -- envoyez votre candidature a Bavarian Nordic Berna GmbH aujourd'hui.",
    "datePosted": "2026-06-04",
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Maintenance Technician/ Instandhaltungstechniker (w/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Vous cherchez un emploi de Maintenance Technician/ Instandhaltungstechniker (w/m/d) a Bern ? Bavarian Nordic Berna GmbH recrute. Für uns geht es darum, Leben z…

Bern Chimie / Pharma Service technique / Entretien
Pubblicato il 03 Jun 2026 👁 16 visualizzazioni
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    "title": "Maintenance Technician/ Instandhaltungstechniker (w/m/d)",
    "description": "Vous cherchez un emploi de Maintenance Technician/ Instandhaltungstechniker (w/m/d) a Bern ? Bavarian Nordic Berna GmbH recrute.\n\nFür uns geht es darum, Leben zu verbessern und zu retten\nAn unserem Standort nahe Bern expandieren wir nicht nur - wir erreichen einen wichtigen Meilenstein, indem wir neue Produktionsräume errichten und innovative Arbeitsweisen einführen. Genau darum geht es, wenn wir den Grundwert „Persistent Pioneer\" unserer BN-DNA leben: Wir bringen Pioniergeist in alles ein, was wir tun. Egal, ob du bereits breite Erfahrung mitbringst, aus der Wissenschaft oder aus einer verwandten Branche kommst; du hast die einmalige Gelegenheit, mit deiner Arbeitsweise diesen nächsten Wachstumsschritt mitzugestalten und zu beeinflussen.\nBavarian Nordic sucht zur Verstärkung des Engineering Teams eine/n\nMaintenance Technician/ Instandhaltungstechniker (w/m/d)\n(Befristung bis 12/2026)\nDiese Rolle ist verantwortlich für die Durchführung von präventiven und korrektiven Wartungsarbeiten an Produktionsanlagen, Versorgungssystemen und kritischen Utilities in einer biopharmazeutischen Produktionsumgebung.\nDas erwartet dich:\n•\nDurchführung von Inspektions-, Wartungs- und Reparaturarbeiten\n•\nAnalyse von Anlagenstörungen sowie Fehlerbehebung\n•\nDokumentation der durchgeführten Arbeiten\n•\nUnterstützung bei der Inbetriebnahme neuer Anlagen\nDas bringst du mit:\n•\nAbgeschlossene technische Ausbildung (z. B. als Industriemechaniker oder Polymechaniker) oder eine vergleichbare Qualifikation\n•\nErfahrung in der Instandhaltung, vorzugsweise in der pharmazeutischen oder biotechnologischen Industrie\n•\nFliessende Deutschkenntnisse; Englischkenntnisse von Vorteil\n•\nGrundkenntnisse in MS-Office-Anwendungen\nEs erwartet dich ein dynamisches und anpassungsfähiges Arbeitsumfeld, das die Entwicklung deiner persönlichen und professionellen Fähigkeiten unterstützt.\nHaben wir dein Interesse geweckt?\nDann freuen wir uns auf deine Bewerbung! Klicke einfach auf die Schaltfläche „APPLY\" und du wirst zu unserem Bewerbungsformular weitergeleitet. Wir führen fortlaufend Bewerbungsgespräche und empfehlen dir, dich so schnell wie möglich zu bewerben. Wir freuen uns auf deinen ausführlichen Lebenslauf inklusive Motivationsschreiben, in dem du kurz dein Interesse für diese bestimmte Stelle erläuterst.\nBewerbungen per E-Mail können leider nicht berücksichtigt werden.\nWir bitten Headhunter und Personalvermittlungsagenturen, uns bezüglich dieser Position nicht zu kontaktieren.\nBavarian Nordic is a global vaccine company with a fonction to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bavarian-nordic.com\nBavarian Nordic\n\nVotre prochaine etape professionnelle commence ici.",
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CSV Professional in QC (f/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Bavarian Nordic Berna GmbH recrute un(e) CSV Professional in QC (f/m/d) a Bern. Are you passionate about quality and data integrity in the laboratory environme…

Bern Chimie / Pharma Gestion / Management Qualité
Pubblicato il 30 May 2026 👁 14 visualizzazioni
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    "title": "CSV Professional in QC (f/m/d)",
    "description": "Bavarian Nordic Berna GmbH recrute un(e) CSV Professional in QC (f/m/d) a Bern.\n\nAre you passionate about quality and data integrity in the laboratory environment? Do you want to make a real impact on QC processes and ensure reliable, compliant data across our site?\nAt our site in Bern you will act as the subject matter expert responsible for ensuring compliance of QC processes and equipment related to data generation, processing, transfer and storage.\nYour tasks\n•\nAct as subject matter expert for computer system validation (CSV) processes within QC and support the implementation of data integrity requirements\n•\nManage the administration and lifecycle of computerized systems and the local LIMS within Quality Control\n•\nServe as process owner for analytical equipment qualification and technical lead for CSV activities in QC\n•\nEnsure the validated status of the local LIMS throughout its entire lifecycle, including system administration and periodic reviews\n•\nCoordinate and support the implementation of system changes within the local LIMS, including computerized system validation activities\n•\nRepresent QC data governance processes during inspections and audits\nAbout you\n•\nBackground in a scientific, technical or related field through education, training or professional parcours professionnel\n•\nProfessional experience working in a cGMP-regulated environment\n•\nFluent in both written and spoken English and German\n•\nBackground in computer system validation (CSV), data integrity and administration of computerized systems in cGMP environments is considered an advantage\nWe provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and professional skills.\nAre you ready to join us in our mission?\nIf this sounds like the next step in your career, simply click the \"APPLY\" button and you will be redirected to our application form. We are conducting interviews on an ongoing basis and encourage you to apply as soon as possible.\nApplications submitted via email will not be considered.\nWe kindly request that headhunters or recuitment agencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a fonction to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bavarian-nordic.com\nBavarian Nordic\n\nInteressé(e) ? Postulez directement sur notre site.",
    "datePosted": "2026-05-30",
    "validThrough": "2026-06-29",
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Operator Biological Manufacturing (w/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Rejoignez Bavarian Nordic Berna GmbH en tant que Operator Biological Manufacturing (w/m/d) a Bern. Für uns geht es darum, Leben zu verbessern und zu retten An …

Bern Chimie / Pharma Pharma R&D / Analyse / Production
Pubblicato il 11 May 2026 👁 16 visualizzazioni
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    "@id": "https://ch-jobs.com/job/operator-biological-manufacturing-w-m-d#jobposting",
    "title": "Operator Biological Manufacturing (w/m/d)",
    "description": "Rejoignez Bavarian Nordic Berna GmbH en tant que Operator Biological Manufacturing (w/m/d) a Bern.\n\nFür uns geht es darum, Leben zu verbessern und zu retten\nAn unserem Standort nahe Bern expandieren wir nicht nur - wir erreichen einen wichtigen Meilenstein, indem wir neue Produktionsräume errichten und innovative Arbeitsweisen einführen. Genau darum geht es, wenn wir den Grundwert „Persistent Pioneer\" unserer BN-DNA leben: Wir bringen Pioniergeist in alles ein, was wir tun. Egal, ob du bereits breite Erfahrung mitbringst, aus der Wissenschaft oder aus einer verwandten Branche kommst; du hast die einmalige Gelegenheit, mit deiner Arbeitsweise diesen nächsten Wachstumsschritt mitzugestalten und zu beeinflussen.\nBavarian Nordic sucht zur Verstärkung des Produktionsteams mehrere\nOperator Biological Manufacturing (w/m/d)\nDas erwartet dich:\n•\nVorbereitung, Bedienung und Reinigung von Prozessanlagen (Bioreaktoren, TFF, Fill& Freeze, Homogenisator, etc.)\n•\nDurchführen und Protokollierung von Produktionsaktivitäten inkl. Linienfreigabe in der Impfstoffherstellung gemäss Richtlinien/SOPs und den Qualitätsrichtlinien nach cGMP\n•\nDurchführen von Raum- und Utilities Monitoring\n•\nMithilfe bei Prozess- und Reinigungsvalidierungen sowie Qualifizierungen\n•\nDokumentation und durchführen von Inprozesskontrollen sowie deren Auswertung\n•\nMithilfe bei der Mitarbeiterschulung und Qualifizierung\n•\nVerwalten, Bewirtschaften und Instandhaltung von zugeteilten Räumen, Einrichtungen und Ausrüstung\n•\nMithilfe bei der Implementierung von neuen Herstellverfahren zur Impfstoffherstellung im Bereich Upstream oder Downstream inklusive Mithilfe bei der Qualifizierung von relevanten Prozessen und Anlagen\nDas bringst du mit:\n•\nAbgeschlossene Berufslehre Lebensmittel- oder Pharmabereich oder einschlägige Berufserfahrung\n•\nBerufserfahrung in Reinräumen (Klasse D und C von Vorteil) gemäss GMP\n•\nGute Kenntnisse im hygienischen Arbeiten (steriles Arbeiten unter cGMP von Vorteil)\n•\nZuverlässiges und exaktes Arbeiten / Protokollieren selbständig und im Team gemäss GDP\n•\nWünschenswert ist Erfahrung im Raum und Utilities Monitoring\n•\nGute Kenntnisse in Deutsch in Wort und Schrift, Englisch von Vorteil\n•\nTeamfähigkeit\n•\nBereitschaft zur Wochenendarbeit\nWir bieten dir die Möglichkeit, Teil eines internationalen Unternehmens zu werden, das sich durch fortschrittliche Technologien und ein spannendes Tätigkeitsgebiet auszeichnet. Es erwartet dich ein dynamisches und anpassungsfähiges Arbeitsumfeld, das die Entwicklung deiner persönlichen und beruflichen Fähigkeiten unterstützt. Dazu gehören ein umfangreiches Leistungspaket und eine wettbewerbsfähige Vergütung.\nHaben wir dein Interesse geweckt?\nDann freuen wir uns auf deine Bewerbung! Klicke einfach auf die Schaltfläche „APPLY\" und du wirst zu unserem Bewerbungsformular weitergeleitet. Wir führen fortlaufend Bewerbungsgespräche und empfehlen dir, dich so schnell wie möglich zu bewerben. Wir freuen uns auf deinen ausführlichen Lebenslauf, in dem du kurz dein Interesse für diese bestimmte Stelle erläuterst. Ein Motivationsschreiben ist optional.\nFür die Rekrutierung dieser Position sehen wir von einer Zusammenarbeit mit Stellenvermittlungen ab.\nBavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bavarian-nordic.com\n#LI-PP1\nBavarian Nordic\n\nInteressé(e) ? Postulez directement sur notre site.",
    "datePosted": "2026-05-11",
    "validThrough": "2026-06-10",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/operator-biological-manufacturing-w-m-d",
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QA Specialist (f/m/d) - CSV & QV

🕐 Tempo pieno 🏢 In sede 📍 Bern

Vous cherchez un emploi de QA Specialist (f/m/d) - CSV & QV a Bern ? Bavarian Nordic Berna GmbH recrute. In Bern, we're not just expanding-we're reaching a maj…

Bern Chimie / Pharma Gestion / Management Qualité
⏳ Scade il 30/07/2026 Pubblicato il 01 May 2026 👁 15 visualizzazioni
{ } JSON-LD
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    "title": "QA Specialist (f/m/d) - CSV & QV",
    "description": "Vous cherchez un emploi de QA Specialist (f/m/d) - CSV & QV a Bern ? Bavarian Nordic Berna GmbH recrute.\n\nIn Bern, we're not just expanding-we're reaching a major milestone by launching a new production site and introducing innovative ways of working. This is what being a Persistent Pioneer in our BN DNA is all about-bringing a pioneering spirit to everything we do. Whether you're an experienced professional, transitioning from academia, or coming from a related industry, you'll have the unique opportunity to influence how we work and grow.\nBoost our team\nIn this key role, you will help ensure high quality standards and contribute to the delivery of safe and effective pharmaceutical products.\nIn this role you will oversee and provide leadership for all Computer System Validation (CSV) activities, as well as Qualification, and Validation (QV) processes at the site. You will ensure compliance with regulatory requirements, internal quality policies and industry best practices, supporting the development and manufacture of safe, effective and compliant products.\nYour tasks\n•\nDevelop, review and approve CSV and QV strategies, plans, protocols and reports for new and existing facilities, utilities, equipment and computerized systems\n•\nPartner with cross-functional teams such as Engineering, Manufacturing, IT and other Quality services to ensure compliance and timely project execution\n•\nParticipate in audits and inspections in relation to CSV and QV, ensuring readiness and robust documentation\n•\nDrive a culture of quality, compliance and continuous improvement within CSV and QV activities, mentoring team members and stakeholders as needed\n•\nSupport changes and corrections in relation with CSV and QV\n•\nAct as subject matter expert (SME) for relevant regulations and guidelines, including EU GMP (EudraLex Volume 4, Annex 11 and 15) and FDA 21 CFR Part 11\nAbout you\n•\nUniversity degree in engineering, life sciences, computer science or a related field\n•\nMinimum 5 years of experience in CSV and ideally QV within the pharmaceutical, biotechnology or related regulated industry; Experience in QA would be a plus\n•\nDemonstrated capability to drive and coordinate complex validation projects in a cross-functional environment with multiple stakeholders\n•\nIn-depth knowledge of cGMP, GAMP, FDA, EMA and other relevant regulations and guidelines\n•\nStrong technical writing, problem-solving, and project management skills\n•\nExcellent written and spoken English skills; German is an advantage, combined with strong interpersonal and communication abilities\nWe provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and professional skills.\nAre you ready to join us in our mission?\nIf this sounds like the next step in your career, we would love to hear from you. Simply click the \"APPLY\" button on the right side of the page and you will be redirected to our application form. We are conducting interviews on an ongoing basis and encourage you to apply as soon as possible.\nA cover letter is not required; however, you are welcome to include one to share additional information about your experience and motivation.\nApplications submitted via email will not be considered.\nWe kindly request that headhunters or recuitment agencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.\nFor more information, visit www.bavarian-nordic.com\nBavarian Nordic\n\nCe poste est a pourvoir rapidement. Candidatez sans tarder.",
    "datePosted": "2026-05-01",
    "validThrough": "2026-07-30",
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        }
    }
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Validation Engineer in MSAT (f/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Vous cherchez un emploi de Validation Engineer in MSAT (f/m/d) a Bern ? Bavarian Nordic Berna GmbH recrute. For us, it is all about improving and saving lives …

Bern Chimie / Pharma Pharma R&D / Analyse / Production
⏳ Scade il 30/07/2026 Pubblicato il 01 May 2026 👁 19 visualizzazioni
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    "title": "Validation Engineer in MSAT (f/m/d)",
    "description": "Vous cherchez un emploi de Validation Engineer in MSAT (f/m/d) a Bern ? Bavarian Nordic Berna GmbH recrute.\n\nFor us, it is all about improving and saving lives\nAt Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial product portfolio includes market-leading vaccines against mpox, rabies, tick-borne encephalitis, typhoid fever, cholera, and chikungunya. We excel in R&D innovation, manufacturing, and commercialization, striving to improve health and quality of life for people worldwide, protecting our tomorrow. Join us in our responsabilite to make a difference.\nWe are looking to strengthen the MSAT Validation Team with a Validation Engineer in MSAT (f/m/d).\nAbout the role\nThe role within the Manufacturing, Science and Technology (MSAT) team focuses on process, cleaning and shipping validation for biotechnological products, including Process Performance Qualification (PPQ) campaigns and commercial production. It involves leading technical investigations, supporting Manufacturing Support Engineers and ensuring continued process verification.\nKey responsibilities include validation planning and execution support, data collection and analysis, identification of trends, troubleshooting, process improvement and preparation of validation reports.\nYou will be part of the MSAT Validation Team, which brings a broad background and parcours professionnel. The team is highly collaborative and open-minded with a great team spirit. Your primary workplace will be in Thörishaus (close to Bern) in a shared office space. We believe in flexibility and offer the possibility to partially work from home, depending on the tasks.\nYour tasks\n•\nPerform all functions associated with process-, cleaning- and shipping validation (definition of validation strategy, planning, writing of plans/ protocols, execution support, evaluation of data and writing reports)\n•\nAuthor and lead process risk analysis and define process control strategy\n•\nRepresent as Validation Subject Matter Expert (SME) on global project teams and validation councils\n•\nRepresent as Validation SME on internal teams (e.g. investigation and project teams)\n•\nAuthor and support of deviations/ investigations and change controls in manufacturing\n•\nMake recommendations for process changes and sponsor these to the larger process team, lead the implementation of the respective change controls\n•\nPerform process monitoring (control charts) and statistical process analysis including authoring of continued process verification reports (CPV)\n•\nProvide data, analyses, write-ups, reviews, and other input to annual Product Quality Reviews (PQR)\n•\nParticipate in internal, customer and regulatory inspections\n•\nSupport Technology Transfer projects as receiving or sending process SME\n•\nActively drive Operational Excellence and Environmental Health and Safety improvements\nAbout you:\n•\nBachelor's degree or higher in Life Sciences\n•\nHighly autonomous and initiative\n•\nExcellent written (especially technical writing) and verbal communication skills in German and English\n•\nExperience with mid and large-scale process- and cleaning validation in GMP regulated Life Science industry (preferably Biotech) is a plus\n•\nCell culture, downstream processing and aseptic manufacturing experiences is a plus\nWe provide an opportunity to be a part of an international company that boasts exceptional technology and a determined team. Join our dedicated and agile MSAT team if you share our enthusiasm and have a desire to create an impact. You can expect a vibrant and adaptable work environment that supports the growth of your personal and technical skills. Additionally, we offer an extensive benefits package and a competitive compensation package.\nAre you ready to join us in our mission?\nIf this sounds like the next step in your career, we would love to hear from you. Simply click the \"APPLY\" button on the right side of the page and you will be redirected to our application form. We are conducting interviews on an ongoing basis and encourage you to apply as soon as possible.\nWe look forward to receiving your CV, including your motivation for applying for this particular position. A cover letter is optional.\nApplications submitted via email will not be considered.\nWe kindly request that headhunters or recuitment agencies refrain from contacting us regarding this position.\nBavarian Nordic is a global vaccine company with a perimetre to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.\nBavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated again",
    "datePosted": "2026-05-01",
    "validThrough": "2026-07-30",
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IT Supporter (m/f/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

IT Supporter (m/f/d) Are you passionate about solving technical challenges and providing support to colleagues in a dynamic environment? Do you want to be par…

Bern Chimie / Pharma Informatique (IT) / T l comm. IT Supporter (m/f/d)
⏳ Scade il 22/07/2026 Pubblicato il 23 Apr 2026 👁 18 visualizzazioni
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    "title": "IT Supporter (m/f/d)",
    "description": " IT Supporter (m/f/d)  Are you passionate about solving technical challenges and providing support to colleagues in a dynamic environment? Do you want to be part of a company that makes a real difference to global health? Bavarian Nordic is looking for a dedicated and service-minded IT Supporter to join our team in Bern.   Are you our next pioneer?  As our IT Supporter, you will be the first point of contact for our internal users, providing support and assisting with smaller projects as needed. You will play a key role in ensuring stable and efficient IT operations throughout the organization together with one team member. You will support users in a pharmaceutical and biotechnology environment, where many systems and processes are subject to GxP (Good Practice) regulations. You will not be responsible for compliance yourself, but it is important to understand the context in which our users work. We provide training in the GxP-related matters relevant to IT support.   Your tasks:    Handle support requests and provide support on hardware, software and networks   Troubleshoot and resolve issues with Windows, Office 365, printers, mobile devices and business applications   Escalate complex cases to other departments and update ITSM documentation   Assist with onboarding/offboarding including user account and device setup   Support IT projects and ensure GxP compliance in regulated environments     About you:    Experience from a similar IT support role, preferably in a regulated company   Knowledge of Windows 10/11, Microsoft 365, Active Directory and networking   Familiarity with ITIL processes and ticketing systems   Good communication skills in English and German   A proactive, service-oriented approach   Ability to work independently and learn about GxP     About Bavarian Nordic  Improving and saving lives through innovative vaccines is at the heart of everything we do at Bavarian Nordic. We are a fully integrated vaccines company focused on developing, manufacturing and commercializing life-saving vaccines and we are the largest pure vaccines company in the world. At Bavarian Nordic, we believe in the power of teamwork, and you will become part of a global team of over 1,800 dedicated employees with diverse backgrounds and perspectives, united by our shared commitment to protecting lives every day. We believe in creating an inclusive and flexible workplace with a strong focus on personal and professional development, because we need each other to move forward. We operate in a world of constant change and are always exploring new opportunities. So, if you are open-minded and have the will to succeed, we might be the perfect match for you.   Ready to make a difference? Apply now!  We hold ongoing interviews and look forward to receiving your CV in english. Applications submitted via email will not be considered.  We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position.   Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.  Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. For more information, visit www.bavarian-nordic.com #LI-PP1Bavarian Nordic",
    "datePosted": "2026-04-23",
    "validThrough": "2026-07-22",
    "employmentType": "FULL_TIME",
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}

Lab Technician QC Microbiology (f/m/d)

🕐 Tempo pieno 🏢 In sede 📍 Bern

Lab Technician QC Microbiology (f/m/d) For us, it is all about improving and saving lives At our site near Bern, we are expanding our production capacity …

Bern Chimie / Pharma Chimie / Pharma / Biotechnologie Chimie R&D / Analyse / Production
⏳ Scade il 30/06/2026 Pubblicato il 01 Apr 2026 👁 32 visualizzazioni
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    "title": "Lab Technician QC Microbiology (f/m/d)",
    "description": " Lab Technician QC Microbiology (f/m/d)    For us, it is all about improving and saving lives   At our site near Bern, we are expanding our production capacity for the manufacture of new vaccines and reaching another milestone in the expansion of a new facility and the introduction of innovative ways of working. This is what living the core value \"Persistent Pioneer\" of our BN DNA is all about: We bring a pioneering spirit to everything we do. Whether you already have broad experience, come from science or a related industry, you have the unique opportunity to shape and influence this next step of growth with your way of working.  At Bavarian Nordic Berna GmbH, our Swiss production site, 215 employees in production, quality control, quality assurance, process development, engineering and supply chain work closely together every day to produce vaccines that help save lives worldwide.  To complement our team in the Quality Control department, we are looking for a Lab Technician QC Microbiology (f/m/d).   You will be part of a talented and collaborative team that works closely with production, quality assurance and supply chain. Our team consists of experienced professionals and new members. This creates a diverse and balanced environment where everyone can learn from each other. We are proud of our team spirit and mutual support is a matter of course for us.   What you can expect:  As part of our microbiological quality control team, you'll work in a dynamic and collaborative environment where high standards and innovation go hand in hand. Your responsibilities will include:   Performing microbiological analyses in compliance with cGMP regulations   Supporting method validations and scientific studies   Accurately documenting all activities in line with cGMP requirements   Maintaining and handling laboratory equipment and tools in a compliant and responsible manner   Contributing to innovative improvement projects that enhance our processes and efficiency     About you:    Completed vocational training, ideally as a biology or chemistry lab technician   Hands-on experience with microbiological testing in a regulated (GxP) environment   Strong motivation, team spirit, and a structured, independent working style   A careful, safety-conscious, and reliable approach to laboratory work   Quick understanding of various analytical methods and electronic systems   Full Proficiency in German and English (spoken and written)    You can expect a dynamic and adaptable working environment that supports the development of your personal skills. In addition, we offer a comprehensive benefits package and a competitive salary.   Have we piqued your interest?   Then we look forward to receiving your application!  Applications submitted via email will not be considered. We kindly request that headhunters or recuitment agencies refrain from contacting us regarding this position.  Founded in 1994, we have +30 years of experience developing life-saving vaccines. We are a global leader in smallpox and mpox vaccines. Our commercial product portfolio contains market-leading vaccines against rabies, tick-borne encephalitis, cholera, typhoid, and Ebola. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America. Our values - our Bavarian Nordic DNA, as we like to call it - are what guide our actions every day. We act as persistent pioneers, embrace change, value being boosted by the team, and believe in protecting lives every day. If that is also a part of your DNA, we invite you to join us in Bavarian Nordic! Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.www.bavarian-nordic.comBavarian Nordic",
    "datePosted": "2026-04-01",
    "validThrough": "2026-06-30",
    "employmentType": "FULL_TIME",
    "url": "https://ch-jobs.com/job/lab-technician-qc-microbiology-f-m-d",
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}

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