# 4,634 Jobs in Switzerland (September 2026) - Find & Apply with AI > Browse verified jobs in Switzerland. Explore 4,634 active roles updated daily. Apply in one click with the LiftmyCV AI Agent. Canonical HTML: https://www.liftmycv.com/jobs/switzerland-jobs/ Markdown: https://www.liftmycv.com/jobs/switzerland-jobs.md Site: https://www.liftmycv.com/ 4,634 Jobs in Switzerland (September 2026) - Find & Apply with AI Explore jobs across Switzerland in September 2026, including opportunities that may span office-based, hybrid, and remote workplace setups. This page is built for a broad Switzerland job search, so candidates can review openings across role families rather than a single profession. Create an account to explore the full job feed and auto-apply with LiftmyCV AI Agent. ## Expert Marina Galkina, Senior HR Manager, Lead Tech Recruiter, and Career Consultant https://www.linkedin.com/in/marina-galkina-148b93224/ "Switzerland in 2026 tends to reward precision in applications. Employers across tech, operations, finance, life sciences, and commercial roles often read for clear scope, language fit, work authorization context, and evidence of delivery in regulated or international settings. Zurich, Geneva, Basel, Lausanne, and Bern can each feel like distinct hiring markets, so candidates usually need to show both role depth and a practical reason for targeting Switzerland, not just a general interest in moving." Marina's Market Take Senior HR Leader & Lead Tech Recruiter ### How to Land a Job in Switzerland in 2026 For jobs in Switzerland, your application needs to answer a few practical questions quickly: where you can work, which languages you can use professionally, and whether your background fits the expectations of Swiss employers. Be clear about your work authorization, notice period, preferred canton or city, and openness to hybrid, on-site, or remote arrangements within Switzerland. Because this page covers jobs across Switzerland, position yourself by lane before you apply. A software engineer should lead with shipped systems, cloud tools, code ownership, and production support. A finance, compliance, or operations candidate should show accuracy, documentation habits, stakeholder coordination, and experience with regulated processes. A sales, customer success, or partnerships candidate should make language coverage, territory experience, account size, and client-facing outcomes easy to find. Product, design, and analytics candidates should connect their work to user research, roadmap decisions, dashboards, experiments, or cross-functional delivery. - **Match the location details.** If a role is listed in Zurich, Geneva, Basel, Lausanne, Bern, or Zug, mention your connection to that area, commute range, relocation plan, or Swiss remote preference. - **State language ability plainly.** Use practical labels such as professional German, fluent French, native Italian, or business English, especially when applying across different Swiss regions. - **Show role fit in Swiss terms.** Employers often value precision, reliability, documentation, and clear ownership, so connect your examples to delivery quality, compliance, client trust, or operational discipline. - **Prioritize credible matches.** Focus first on jobs in Switzerland where your sector, tools, seniority, language profile, and work location line up closely with the listing. For **jobs in Switzerland**, your resume should make location fit easy to read: Swiss work authorization, city or relocation plans, and working languages such as German, French, Italian, or English when they apply. Keep the top section practical, with role title, core tools, and industry context rather than a long profile paragraph. Highlight proof that matches the function. Product and project roles should show launches, timelines, Jira or Confluence use, stakeholder groups, and certifications such as PMP, PRINCE2, or Scrum when relevant. Finance, operations, and compliance resumes should emphasize controls, reporting, audits, SAP, Excel, risk processes, and regulated-environment experience. Sales, marketing, and customer roles should show pipeline, CRM work in Salesforce or HubSpot, regional accounts, campaigns, retention, or support metrics. Cut vague claims, old coursework, and tool lists you cannot defend in an interview. - Weak bullet: “Responsible for project coordination and reporting.” - Strong bullet: “Coordinated a cross-functional rollout across product, finance, and operations teams, using Jira and weekly status reporting to keep 2026 milestones visible to Swiss and regional stakeholders.” Use concise bullets, name the systems you used, and connect each result to the type of Swiss employer you’re targeting, whether that’s a bank, pharma company, manufacturer, SaaS firm, nonprofit, or public-sector organization. For Jobs in Switzerland, prepare for interviews that test both role depth and how you work across multilingual, regulated, and often international teams. If you’re interviewing for engineering or data roles, expect a technical screen, coding exercise, analytics task, or system design discussion where you explain tradeoffs clearly. Product, growth, and operations interviews may use a case prompt, such as prioritizing a rollout for Swiss and EU users with limited team capacity. Bring examples that show measurable work: a product launch, process improvement, compliance review, support workflow, sales pipeline change, or research project with clear outcomes. For design roles, prepare a concise portfolio review that covers user problem, constraints, iterations, and results. For finance, compliance, legal, or operations roles, practice walking through risk, documentation, stakeholder approvals, and decision records. In 2026, interviewers for Switzerland-based roles may also probe communication style, language expectations, remote or hybrid collaboration, and comfort working across Zurich, Geneva, Basel, Lausanne, or distributed European teams. ## Salary Data for Jobs in Switzerland (September 2026) Review salary information for jobs in Switzerland based on the roles currently listed on LiftmyCV. This section uses 4,634+ active postings as context where salary details are available. | Level | P25 | P50 | P75 | | --- | --- | --- | --- | | Average | 93923.75 | 146950 | 201500 | | Entry | 50500 | 70000 | 100400 | | Mid | 88512.5 | 125000 | 175000 | | Senior | 141632.5 | 177500 | 226749 | Skills: ["customer service","sales support","account management","administration","operations coordination","project management","data analysis","reporting","business development","CRM","stakeholder management","process improvement","financial analysis","budgeting","compliance","documentation","Microsoft Excel","SAP","supply chain","procurement","marketing campaigns","content management","technical support","quality assurance"] ## Example jobs - **Senior Scientist QC Bioanalytics (m/w/d) 80-100% — Lonza AG — CH - Visp**: **Location:**Visp (Switzerland) Relocation assistance is available for eligible candidates and their families, if needed. Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of! At the Visp site, we are looking for a Scientist (m/f/d). As a member of our great Quality Control team, you will be responsible for the routine execution of various biochemical methods, focusing on ELISA, qPCR, ProA and enzyme assays, while adhering to GMP and safety guidelines. **What you’ll get:** - An agile career and dynamic working culture - An inclusive and ethical workplace - Compensation programs that recognize high performance - Along with competitive salaries, you’ll find a wide range of lifestyle, family and leisure benefits available. The full list of our local benefits can be also found on [assetstream.aspx](https://dam.lonza.com/dmm3bwsv3/assetstream.aspx?assetid=19443&mediaformatid=10061&destinationid=10016&cat=Employer%20Brand) **Key responsibilities**: - Preparation of qualification, calibration, maintenance plans in line with GMP and regulatory requirements. (IQ, OQ, PQ) according to guidelines and procedures. Verify proper installation of instruments (SpectraMax, qPCR, ViaCell etc.) according to manufacturer specifications and GMP standards. - Validation of SMP Templates - Performing ERAS and DIRAS according guidelines. Ensure all qualification data is accurate, complete, secure, and compliant with data integrity principles - Ensuring communication with the responsible QUS, IT, QA and QC employees. Awareness of software lifecycle management, including validation, updates, patches, and version control, ensuring continued compliance with GMP requirements. - Knowledge of electronic data capture, storage, backup, and retrieval processes to ensure compliance with data integrity principles (ALCOA+). Ability to interpret system logs, error messages, and diagnostic tools to identify and resolve software or hardware issues during maintenance and qualification - Ensure ongoing compliance with GMP through audits and continuous process improvements. Familiarity with regulatory guidelines relating to computerized systems in GMP environments, such as FDA 21 CFR Part 11 and EU Annex 11. - Understanding of how instruments/robots interface with Laboratory Information Management Systems (LIMS) or other relevant platforms. **Key requirements:** - Bachelor/Master in science or equivalent - Solid experience with quality control laboratory instruments (e.g. SpectraMax, qPCR, ViaCell) - Solid experience in the pharmaceutical industry in a GMP environment is a must - Good knowledge of analytical instrument qualification (AIQ), as well good background of CSV (computer system validation) - Experience and understanding with software, IT programs - Structured, focused and well-organized working attitude. Open-minded for new ideas and suggestions, highly motivated and dynamic drive. Teamwork, as well flexibility for various tasks in technology team - Good verbal and written communication in English Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. - **Bioprocess Engineer Automatisierung in der pharmazeutischen Produktion (m/w/d) (Offen) — Lonza AG — CH - Visp**: Der Arbeitsort dieser Stelle befindet sich in Visp, Schweiz. Anspruchsberechtigten Bewerbern und ihren Familien steht bei Bedarf Unterstützung beim Umzug zur Verfügung. An unseren Standort in [Visp](https://www.youtube.com/watch?v=jFPysvXnuBU&feature=youtu.be) suchen wir für den Bereich der chemischen Pharmaproduktion Visp MES(Syncade)/DCS(DeltaV) Spezialisten. Diese Stelle erfordert eine durchgehende Präsenz vor Ort. Die persönliche Zusammenarbeit ermöglicht eine enge, zeitnahe Zusammenarbeit und die technische Präzision, die für die Herstellung von Arzneimitteln nach höchsten Qualitäts- und Sicherheitsstandards erforderlich ist. **Was wir bieten:** - Eine agile Karriere und eine dynamische Arbeitskultur - Ein integratives und ethisches Arbeitsumfeld - Vergütungsprogramme, die hohe Leistung anerkennen - Eine Vielzahl von Vorteilen, abhängig von Funktion und Standort. Die vollständige Liste unserer globalen Vorteile finden Sie hier: [https://www.lonza.com/careers/benefits](https://www.lonza.com/careers/benefits). **Ihre Aufgaben:** - Sie erstellen, testen und optimieren den automatisierten Produktionsablauf. - Enge Zusammenarbeit mit dem zuständigen Anlageteam (Chemiker, Anlage- und Automationsingenieur, QA Manager, Anlagemeister) während der Planungsphase und der Produktion. - Erstellung und Anpassung von Rezepturen im DeltaV und MES. - Teilnahme an Risiko- und Prozessabweichungsanalysen. - In Zusammenarbeit mit anderen Abteilungen stellen Sie die cGMP-gerechte Dokumentation sicher. - Sie verbessern ständig Abläufe und Prozesse unter Einhaltung der Sicherheits-, Hygiene-, Umwelt- und Qualitätsanforderungen. - Sie erkennen Risiken in Bezug auf Sicherheit oder Compliance/GMP, thematisieren diese und arbeiten mit bei deren Behebung. **Was wir suchen:** - Fundierte Erfahrung in der Verfahrenstechnik und Produktion und/oder im Erstellen von DeltaV und MES Rezepten (Syncade). - Bereitschaft zur internen Weiterbildung zum MES/DeltaV Spezialisten. - Die Zusammenarbeit mit internen Schnittstellen und den Teammitgliedern gehört zu Ihren Stärken - Sie sind ein Planungs- und Organisationstalent bei komplexen Projekten und haben eine stets lösungsorientierte Arbeitsweise - Sie sprechen deutsch und haben Grundkenntnisse in Englisch. **Über Lonza** Bei Lonza sind unsere Mitarbeiter unsere grösste Stärke. An über 30 Standorten auf fünf Kontinenten arbeiten unsere global vernetzten Teams täglich zusammen, um die Medikamente von morgen herzustellen. Unsere Grundwerte: Zusammenarbeit, Verantwortlichkeit, Exzellenz, Leidenschaft und Integrität spiegeln wider, wer wir sind und wie wir zusammenarbeiten. Die Ideen jedes Einzelnen, ob gross oder klein, haben das Potenzial, Millionen von Leben zu verbessern, und genau daran möchten wir Sie teilhaben lassen. Innovation gedeiht, wenn Menschen unterschiedlichster Herkunft ihre einzigartigen Perspektiven einbringen. Bei Lonza schätzen wir Vielfalt und setzen uns für ein integratives Umfeld für alle Mitarbeiter ein. Wenn Sie bereit sind, die bahnbrechenden Ideen unserer Kunden in praktikable Therapien umzusetzen, freuen wir uns, Sie an Bord begrüssen zu dürfen. **Bereit die Zukunft der Life Sciences zu gestalten? Jetzt bewerben** - **Senior Scientist — Celgene International SaRL — Boudry - CH**: At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. MS&T is a science-driven organization dedicated to building deep scientific and technical knowledge of our products and processes across the full pharmaceutical lifecycle. The organization supports both internal and external manufacturing and packaging networks, ensuring robust, compliant, and efficient supply. The Senior Scientist, Drug Product & Packaging is an experienced individual contributor who provides strong scientific and technical expertise in support of drug product and packaging processes for commercial and late-stage products. The role focuses on execution, problem solving, and technical depth within defined project scopes and operates with a high degree of autonomy while aligning with strategies and priorities set by senior MS&T leadership. The Senior Scientist is expected to independently handle complex technical assignments, contribute significantly to cross-functional teams, and apply sound scientific judgment to support reliable product supply, compliance, and continuous improvement. **Duties/Responsibilities** - Serve as a subject matter contributor for drug product and packaging processes - Contribute to standards and SOPs ​ - Support investigations and root cause analysis - Contribute to CQAs, CPPs, and control strategies - Design and execute technical and validation studies - Technology Transfer & Lifecycle Management - Support DP and packaging tech transfer - Ensure knowledge capture via TPT - Support lifecycle improvements - Project & Documentation Responsibilities - Own defined technical workstreams - Author and review GMP documentation - Support CMC submissions - Scientific Excellence & Continuous Improvement - Maintain scientific expertise - Drive continuous improvement **Qualifications** Specific Knowledge, Skills, Abilities: - Good working knowledge of QA, cGMP, and the Pharmaceutical Regulatory framework. - Good knowledge of various types of pharmaceutical packaging processes/technologies. - Good knowledge of Technology Transfer and validation. - Working knowledge Lean and 6 Sigma methodologies. - Good leadership skills and ability to influence and work across organizational boundaries. - Effective communication skills, good command of English and preferably another European language. Education/Experience/ Licenses/Certifications: - Minimum bachelor’s degree in Process/Packaging Engineering/Technology, Process/Packaging Development, or similar education in this field. - 5-8 years of experience in the Pharmaceutical/Cosmetics/Food industry. - Experience in the development/application design and their implementation. - Knowledge and experience of pharmaceutical packaging materials. - Demonstrated project leadership. Experience of multi-site/cross-site project management. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. **How We Work** Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at [https://careers.bms.com/ways-of-working.](https://careers.bms.com/life-at-bms/ways-of-working/) **Supporting People with Disabilities** BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [adastaffingsupport@bms.com](mailto:adastaffingsupport@bms.com). Visit [careers.bms.com/eeo-accessibility](https://careers.bms.com/eeo-accessibility) to access our complete Equal Employment Opportunity statement. **Candidate Rights** BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: [https://careers.bms.com/california-residents/](https://careers.bms.com/california-residents/) **Data Protection** We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at [https://careers.bms.com/fraud-protection](http://careers.bms.com/fraud-protection). Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [TAEnablement@bms.com](mailto:TAEnablement@bms.com) with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1606196 : Senior Scientist - **Senior Vice President, Corporate Finance — Lonza Sales AG — CH - Basel**: Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. At Lonza, we are looking for a Senior Vice President, Corporate Finance to provide enterprise-wide leadership across Global Business Services, Corporate Accounting & External Reporting, Group Tax, Group Treasury, and Process Excellence. Reporting directly to the Group CFO, this highly influential leadership role will bring these critical capabilities under unified leadership, strengthening strategic alignment, financial governance, and responsiveness to the evolving needs of the business. Leading a global organization of approximately 360 employees, including a senior leadership team of Vice Presidents, you will shape and execute major finance transformation initiatives, strengthen financial compliance and standardization, and support strategic M&A and business priorities. You will combine deep corporate finance expertise with enterprise leadership to drive operational excellence, enable scalable ways of working, and help shape Lonza's long-term financial strategy and performance. **Key Responsibilities:** - Provide strategic leadership across Global Business Services, Corporate Accounting & External Reporting, Group Tax, Group Treasury, and Process Excellence, ensuring strong alignment and performance across the Corporate Finance organization - Lead and develop a senior leadership team of experienced Vice Presidents and their organizations, fostering collaboration, accountability, functional excellence, and enterprise-wide impact - Drive the transformation and evolution of Lonza's global service delivery model, including further offshoring and nearshoring opportunities across Finance and other functions - Strengthen financial governance, compliance, controls, and standardization, including the continued development of Global Process Ownership across functions - Oversee Group accounting and external reporting, ensuring accurate, timely, and compliant financial reporting and effective engagement with auditors and regulatory stakeholders - Provide strategic leadership across Group Tax and Treasury, including tax efficiency, transfer pricing, Pillar 2 requirements, liquidity, funding, debt management, foreign exchange, and broader financial risk management - Support acquisitions, divestitures, and other strategic transactions, shaping carve-out, purchase price allocation, financing, and tax structures to optimize transaction outcomes - Drive the development of integrated end-to-end commercial offerings, partnering across Finance and Key Account Management on pricing, revenue recognition, invoicing, and trade compliance for cross-platform opportunities - Play a key leadership role in major enterprise transformation initiatives, including SAP S/4HANA implementation and other cross-functional Finance programmes requiring significant organizational alignment - Act as a trusted advisor to the Group CFO and senior leadership, providing strategic insight and clear recommendations while representing Corporate Finance with the Executive Committee, Audit and Compliance Committee, and key external stakeholders **Required qualifications:** - 10+ years of senior Finance leadership experience, with significant responsibility across corporate finance, accounting, treasury, tax, global business services, or related enterprise finance functions - 5–10 years of relevant strategy and M&A transaction experience, including exposure to acquisitions, divestitures, carve-outs, financing structures, or other complex corporate transactions - Proven experience leading large, global Finance organizations and senior executive teams within complex, matrixed multinational environments - Deep expertise in corporate finance, strategic financial management, financial reporting, governance, compliance, controls, and risk management - Demonstrated success leading large-scale Finance transformation, process standardization, shared services, offshoring/nearshoring, or enterprise-wide change initiatives - Strong understanding of major ERP and Finance transformation programmes, with experience supporting complex SAP S/4HANA or comparable implementations highly desirable - Exceptional strategic and commercial acumen, with the ability to connect deep business understanding with functional expertise and translate complex issues into actionable decisions - Strong executive presence and communication skills, with demonstrated ability to influence, build consensus, and partner effectively with C-suite executives, Boards/Committees, auditors, banks, regulators, and other senior stakeholders - Master's degree in Business or a related discipline required; ACCA, CPA, or comparable professional Finance qualification is preferred - Fluency in English is required; German is an advantage. Experience operating across global and culturally diverse organizations is essential Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world — the satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. - **Scientist, Validation & Investigations — Celgene International SaRL — Boudry - CH**: At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. **Position Summary** MS&T is a science-driven organization dedicated to building in-depth and comprehensive knowledge of our products and their processes. We work across the entire lifecycle of our Pharmaceutical Products and support the Boudry internal manufacturing site The Validation & Investigations Scientist is supporting the Boudry manufacturing process units by executing investigation and/or validation activities within MS&T using established scientific principles, contributing to product quality, process robustness, and cGxP compliance. Acts in one or more domain among Equipment Qualification, Cleaning validation, Process validation, Robustness and Investigations. More specifically, the Validation & Investigations Scientist partners with other site and MS&T functions to design and execute procedures that guarantee the robustness of manufacturing processes at internal sites. **Duties/Responsibilities** **Validation, Qualification & Robustness ** - Author validation and qualification documentation, including but not limited to plans, protocols, reports, traceability matrices and summary reports, in accordance with approved strategies, procedures and regulatory requirements. These documents may be in relation with equipment qualification, process validation, cleaning validation, continued process verification. The designed approaches must include scientific rationales and acceptance criteria, and be based on quality risk management principles. - Execute validation, qualification, or robustness activities across the site, including data collection and data analysis. - Support introduction of new products or new technologies on the site, by ensuring associated equipment, systems and processes are qualified, validated and maintained in compliance with local policies, guidelines, and procedures during their lifecycle. - Perform the assessment of change controls and maintenance interventions, evaluating potential impact to qualified systems and validated processes. - Interface with Engineering, Technical Services, Manufacturing, QC, QA and other stakeholders to support MS&T objectives. **Investigations** - Support initial assessments of deviations in order to assist deviation owners to define need for investigations. - Lead and conduct investigations with appropriate methodology until conclusion and ensures that the investigation outcome, root cause analysis and execution of corrective and preventive actions are completed in a timely, effective and compliance manner. Investigation scope may be related to bulk operations, packaging operations, warehouse, or maintenance processes. - Prepare data-driven, scientifically justified, risk-based impact assessment of deviations in order to support their classification, in conjunction with Quality Operations - Provide appropriate level of reporting and communication on the assigned investigations. **General** - Complete all required regulatory, site and department training in a timely manner. - Participate in audits and inspections as a supporting Subject Matter Expert, when required. - Contribute to continuous improvement, including proactively identifying problems, gathering inputs from operational teams and proposing solutions - Contribute to risk assessments as Subject Matter Expert - Provide support to other MS&T projects as required. - May be involved in additional projects/initiatives at site or global level to represent Boudry MS&T Team (EHS, continuous improvement, quality, risk management, etc) **Reporting Relationship** This position reports to the Associate Director of Validation & Investigations Boudry MS&T. **Qualifications** Specific Knowledge, Skills, Abilities: - Ability to constructively work across functional areas and levels. - Strong communication skills - Technical writing skills - Fluent in French and English - Capability to work with short deadlines and simultaneous activities - Strong analytical, problem solving skills Education/Experience/ Licenses/Certifications: - Degree in Engineering, Chemistry, Pharmacy or Natural Science. - Minimum 3 years of experience in pharmaceutical operations, validation, packaging, quality or related field, if possible in Oral Solid Dosage manufacturing. - Solid knowledge of current international regulatory regulations, cGxP requirements and best practices - Experience in Health Authority inspections (preparation, process, presentations, responses drafting, etc.) is a nice to have. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. **How We Work** Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at [https://careers.bms.com/ways-of-working.](https://careers.bms.com/life-at-bms/ways-of-working/) **Supporting People with Disabilities** BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [adastaffingsupport@bms.com](mailto:adastaffingsupport@bms.com). Visit [careers.bms.com/eeo-accessibility](https://careers.bms.com/eeo-accessibility) to access our complete Equal Employment Opportunity statement. **Candidate Rights** BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. For roles based in Los Angeles County only: If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: [https://careers.bms.com/california-residents/](https://careers.bms.com/california-residents/) **Data Protection** We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at [https://careers.bms.com/fraud-protection](http://careers.bms.com/fraud-protection). Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. If this posting is missing required information required by local law or incorrect, contact BMS at [TAEnablement@bms.com](mailto:TAEnablement@bms.com) with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account. R1606086 : Scientist, Validation & Investigations - **Project Management Organization (PMO) Manager 80-100% (f/m/d) — Lonza Sales AG — CH - Basel**: The actual location of this job is in Basel Tower, Switzerland. Due to renovation work at the Tower as of January 2027, the interim location will be Basel Stücki. As PMO Manager, Group Operations, you will be a strategic partner to the Head PMO Group Operations. You will help drive the Group Operations agenda, coordinate key initiatives, enable effective governance, and support executive decision-making. This is an exciting opportunity to influence transformation, operational excellence, and business performance across a global organization. **What you will get:** - An agile career and a dynamic work culture - An inclusive and ethical workplace - Compensation programs that recognize high performance **What you will do:** - Partner with the Head PMO to translate Group Operations strategy into actionable plans and measurable outcomes - Lead and manage the Group Operations strategic project portfolio, ensuring alignment with business priorities - Establish governance processes, performance dashboards, and reporting to track strategic initiatives - Prepare executive presentations, business cases, leadership meeting materials, and decision-support recommendations - Build strong partnerships across Group Operations, Global Functions, and Platforms to drive collaboration and execution - Lead communication and change management activities that support business transformation and organizational priorities - Analyze operational and project performance data, identify improvement opportunities, and drive operational excellence initiatives **What we are looking for:** - Bachelor's or Master's degree in Business Administration, Engineering, Life Sciences, Operations Management, Program Management, or a related field - Proven experience managing complex programs, portfolios, or strategic initiatives in a global environment - Strong project management expertise, including governance, reporting, performance management, and data analytics - PMP certification or an equivalent project management qualification - Excellent communication, presentation, stakeholder management, and problem-solving skills - Proficiency with Microsoft Office applications and project or data analysis tools - Fluency in written and spoken English. Additional languages are an advantage **About Lonza** At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. **Ready to shape the future of life sciences? Apply now.** - **Art Director — Scopely — CH - China**: Scopely is looking for an **Art Director** to join an unannounced title based in our Shanghai office (5 days in the office). At Scopely, we care deeply about what we do and want to inspire play, every day - whether in our work environments alongside our talented colleagues, or through our deep connections with our communities of players. We are a global team of game lovers who are developing, publishing and innovating the mobile games industry, connecting millions of people around the world daily. We are in the early stages of development on an ambitious mobile game in China, and we’re assembling a team of passionate game makers to craft unforgettable characters and immersive adventures that players will love. ### What You Will Do - Partner with the Global Sr. Art Director to execute the visual vision and quality standards for mobile game features, events, and content. - Lead the artistic development of game features from concept through final implementation. - Serve as the primary art liaison with external IP partners by presenting work for review, facilitating feedback and approvals, and ensuring clear communication and alignment between external stakeholders and the internal art team. - Create, review, and provide feedback on art assets to ensure consistency, quality, and adherence to brand standards. - Act as the art representative on cross-functional feature teams, collaborating closely with Design, Product, Engineering, UX, and external partners. - Establish and maintain visual targets, benchmarks, and best practices for content creation. - Supervise outsource vendors, overseeing schedule, assigning work and providing feedback. - Organize and lead art reviews, brainstorming sessions, and creative discussions. - Help improve workflows, pipelines, and production processes in partnership with Technical Art and Engineering. - Identify creative risks and opportunities and communicate recommendations to project leadership. - Contribute directly to production as needed while helping the team deliver high-quality work on schedule. ### What We're Looking For - 6+ years of experience in game development, visual design, or a related creative field. - Experience leading art production for shipped games, live-service products, or major game features. - Strong artistic fundamentals, including composition, color, visual hierarchy, and player-focused design. - Proven ability to provide clear, constructive feedback and mentor artists across disciplines. - Experience working closely with cross-functional teams throughout the development process. - Strong communication, organization, and problem-solving skills. - Knowledge of game development pipelines, content creation workflows, and production processes. - Proficiency with industry-standard art and design tools.. - Possesses 2D/3D generalist skill set, including modeling and rendering. - Proficient experience with Maya. - Experience with Unity 3D. - Ability to work in a fast-paced hybrid environment and handle stress appropriately and/or ability to solve practical problems and be sufficiently adaptable to handle dynamic situations with little advance notice. - Must be proficient in English. **Plus if...** - Experience with JIRA and GIT. - BA or equivalent degree in studio art, computer graphics or technical field. - Minimum 6 years of experience preferred. - Familiarity with top F2P mobile games. Please ensure that the résumé/CV you attach is written in English. ### About Scopely Scopely is a leading video game and global interactive entertainment company, home to many of the world’s most beloved and enduring experiences, including two of the most successful mobile games of all-time “MONOPOLY GO!” and “Pokémon GO,” along with “Stumble Guys,” “Star Trek™ Fleet Command,” “MARVEL Strike Force,” “WWE Champions,” the Scrabble® franchise, “Yahtzee® With Buddies,” and many others. Across mobile, web, PC, and console, Scopely creates, develops, publishes, and live-operates one of the most diversified and award-winning portfolios in the games industry — bringing hundreds of millions of players together through a shared love of play. Founded in 2011, Scopely is powered by its exceptional team — including thousands of world-class gamemakers around the globe, a distinctive tenet-driven culture, and its proprietary technology platform, Playgami. Together, these strengths have fueled Scopely’s position as the #1 mobile games company in the U.S. and #2 globally, generating more than $10 billion in lifetime revenue. Whether building global sensations like “MONOPOLY GO!” from the ground up, or expanding through strategic acquisitions, including the FoxNext, GSN, and Scopely Explore games businesses — Scopely consistently delivers experiences players love today and return to for years to come. Recognized multiple times as one of the "100 Most Influential Companies in the World" by TIME magazine and one of Fast Company's "World's Most Innovative Companies" and “Best Workplaces for Innovators,” Scopely believes that video games can be a force for good — creating meaningful connections, vibrant communities, and making life better through play. Scopely has global operations and partners across four continents in more than a dozen countries worldwide. For more information, visit: [https://www.scopely.com/](https://www.scopely.com/). Notice to Candidates: Scopely will never request payment or financial information during the application or hiring process. Please apply only through our official [website](http://scopely.com) and verify that all Talent Partner communications come from an email address ending in @[scopely.com](http://scopely.com). Should you have any questions or encounter any fraudulent requests/emails/websites, please immediately contact recruiting@scopely.com. Our job applicant privacy policies are available here: [California Privacy Notice](https://www.scopely.com/en/job-applicant-privacy-notice-for-ca-residents) and [EEA/UK Privacy Notice](https://www.scopely.com/en/eea-and-uk-job-applicant-privacy-notice). Employment at Scopely is based solely on a person's merit and qualifications. Scopely does not discriminate against any employee or applicant because of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), or any other basis protected by law. We also consider qualified applicants with arrest or conviction records, consistent with applicable federal, state and local law. - **MSAT Bioconjugates Process Expert (f/m/d) 80-100% — Lonza Group AG Basel — CH - Visp**: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. In this position of MSAT Bioconjugates Process Expert, you will make a difference by being responsible for the successful supervision, support and life cycle management of bioconjugate processes in Lonza’s facilities in Visp. You will play a crucial role in the network between the different departments such as development, manufacturing, quality assurance and quality control. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. **What you will get:** - An agile career and dynamic working culture. - A highly collaborative environment that fosters teamwork and inclusion. - A range of professional programs to develop your skills and your career. - An ethical workplace where tasks are carried out in accordance with the relevant procedures. - In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. You can find the full list of local benefits below:  [https://www.lonza.com/careers/benefits](https://www.lonza.com/careers/benefits). **What you will do:** - Assume the role of MSAT Process Expert for the manufacturing of clinical or commercial bioconjugates by being responsible for the execution of your assigned programs in the best possible time, quality and cost, in compliance with the relevant laws, regulations and guidelines with view on safety, quality, hygiene and the environment. - Assume a crucial role in the network between the different departments. - Deliver all inputs required for your assigned programs from a process and cGMP standpoint. - Own the life cycle management of your assigned programs including technology transfers, scale ups and suite changes. - Lead process troubleshooting on the manufacturing floor and optimize your assigned programs in a continuous manner. - Represent process MSAT in audits and inspections. **What we are looking for:** - Master or PhD or equivalent experience in bioconjugation, biotechnology, chemical engineering, organic chemistry or related fields. - Solid experience in bioconjugation and biopharma manufacturing, preferably in the areas of bioconjugation or DSP (mammalian or microbial). - Preferred cGMP experience. - Excellent communication skills for interaction with customers and within the organization. - Proficient in English; German language skills of advantage. - Motivated, creative, agile and open-minded. - Eager to foster teamwork and inclusion. **About Lonza** At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you are ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. **Ready to shape the future of life sciences? Apply now.** - **Automation Engineer MES/DeltaV — Lonza Group AG Basel — CH - Visp**: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. As a Automation Engineer MES / DeltaV, you will be responsible for the implementation, optimization, and ongoing support of Manufacturing Execution Systems (MES) and Emerson DeltaV process control systems within biopharmaceutical manufacturing facilities. You will play a key role in ensuring efficient production operations, regulatory compliance, and adherence to the highest quality standards This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. **What you will get:** - An agile career with opportunities for professional growth in a global life sciences organization. - A collaborative, inclusive, and ethical workplace where diverse perspectives are valued. - Competitive compensation and recognition programs that reward high performance. - Access to a wide range of local and global benefits, depending on role and location. - Opportunities to work with cutting-edge technologies in biopharmaceutical manufacturing and automation. The full list of our global benefits can be found here: [https://www.lonza.com/careers/benefits](https://www.lonza.com/careers/benefits) **What you will do:** - Design, implement, and validate MES recipes and DeltaV control strategies that support robust and compliant biopharmaceutical manufacturing processes. - Partner closely with Manufacturing, Process Development, Automation, Engineering, and Quality teams to ensure seamless system integration and operational excellence. - Troubleshoot and resolve MES and DeltaV system issues, minimizing production disruptions and supporting reliable plant operations. - Develop and maintain technical documentation, including specifications, work instructions, and validation records in accordance with GMP requirements. - Support end users through training, technical guidance, and ongoing system expertise. - Drive continuous improvement initiatives, identifying opportunities to optimize manufacturing processes, automation strategies, and system performance. - Contribute to the implementation of new technologies and digital manufacturing solutions that enhance productivity, compliance, and operational efficiency. **What we are looking for:** - Experience working in the pharmaceutical, biopharmaceutical, biotechnology, or other highly regulated manufacturing environments. - Strong knowledge of Manufacturing Execution Systems (MES), ideally including Werum PAS-X, Rockwell PharmaSuite, or comparable platforms. - Experience with Emerson DeltaV or other distributed control systems used in process manufacturing. - Understanding of GMP regulations, computerized system validation, and qualification activities in regulated industries. - Ability to analyze complex technical issues, identify root causes, and implement effective solutions. - Strong communication and collaboration skills, with the ability to work effectively across multidisciplinary teams. - A degree in Bioprocess Engineering, Biotechnology, Automation Engineering, Electrical Engineering, or a related technical discipline, or equivalent experience demonstrating these capabilities. **About Lonza** At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board. **Ready to shape the future of life sciences? Apply now.** - **Specialist, Sales Support, Strategic Sales — CH_RSC_L Randstad (Schweiz) AG — CH - Zurich_Thurgauerstrasse**: **Specialist, Sales Support, Strategic Sales** Workload - 60 - 100% **Job Profile Summary** Supports the daily maintenance of the HubSpot CRM system to ensure data accuracy, basic reporting, and user adoption across sales operations. Assists with Compliance & Sustainability data gathering, including EcoVadis inquiries, while supporting ESA process improvements and administrative workflows under the guidance of senior team members. **Job Description** - Maintain and update data within the HubSpot CRM to support accurate daily reporting and user adoption. - Assist in organizing and maintaining filing systems and self-service repositories for ESA processes, utilizing existing automation tools. - Gather input from internal stakeholders and training teams to help identify basic learning needs and administrative gaps. - Generate routine sales operations reports and routine data extracts using standard CRM analytics tools. - Help communicate process or tool updates to sales teams, and assist sales reps with basic budget data entry and template updates. - Follow organizational compliance guidelines, business policies, and standard operating procedures across sales administrative tasks. - Collaborate with cross-functional and international stakeholders to pull routine sales performance data. - Support senior team members in collecting and organizing data required for Compliance & Sustainability reports, audits, and EcoVadis inquiries. **Requirements & Competencies** - Basic working knowledge of CRM systems (HubSpot preferred) and general sales operations concepts. - Ability to work effectively under direct or moderate supervision, executing tasks using defined guidelines. - Strong attention to detail, organization, and a conscientious approach to meeting deadlines. - Proactive, eager to learn, and comfortable working in a fast-paced environment. - Bachelor’s degree in a relevant field or equivalent entry-level professional experience. - Solid written and verbal communication skills. - Fluent in English and German; French language skills are a plus. ## Related - [Jobs in Germany](/jobs/germany-jobs/) - [Jobs in the Netherlands](/jobs/netherlands-jobs/) - [Jobs in Spain](/jobs/spain-jobs/) - [Jobs in Ireland](/jobs/ireland-jobs/) - [Jobs in the UK](/jobs/uk-jobs/) - [Jobs in London](/jobs/london-jobs/) - [Remote Jobs in the UK](/jobs/remote-jobs-uk/) - [Jobs in UAE](/jobs/uae-jobs/) - [Jobs in Dubai](/jobs/dubai-jobs/) - [Jobs in Canada](/jobs/canada-jobs/) - [Jobs in Australia](/jobs/australia-jobs/) - [Jobs in New Zealand](/jobs/new-zealand-jobs/) ## FAQ ### How do I find jobs in Switzerland in 2026? Start with the current Jobs in Switzerland listings and narrow by the details shown on each posting, such as job title, location within Switzerland, and workplace format when available. Since this page is broad, it can include different kinds of openings rather than one fixed role category. Review the description closely before applying so your resume reflects the specific Swiss job listing, not just a general interest in Switzerland. ### Are there remote jobs in Switzerland on this page? Some Jobs in Switzerland listings may mention remote, hybrid, or on-site expectations, but the page title alone does not guarantee a workplace format. Check each posting for the exact arrangement before you apply. A Switzerland-based role can still vary by employer, team setup, and location requirements, so use the listing details rather than assuming every job allows remote work. ### Can I apply to Switzerland jobs from outside the country? You can review Jobs in Switzerland from anywhere, but each employer sets its own application, location, and work authorization requirements. The safest approach is to read the Switzerland job description carefully before applying, especially any notes about local presence, relocation, or eligibility. Avoid treating every listing the same, since a broad Switzerland jobs page can include different hiring contexts. ### What should my resume emphasize for jobs in Switzerland? For Jobs in Switzerland, align your resume with the exact posting rather than using one broad version for every application. Match the job title, required experience, tools, language expectations, and workplace details when they appear in the listing. If the page includes several types of Switzerland openings, adjust the top section of your resume for each role instead of relying on a generic summary. ### Are Switzerland jobs open to entry-level applicants? Entry-level availability depends on the individual Jobs in Switzerland listing. Some postings may ask for limited experience, while others may be written for senior or specialized candidates. Since this page covers Switzerland jobs broadly, check the seniority language in each description, such as assistant, junior, associate, manager, or lead, before deciding whether the opening fits your background in 2026. ### How often should I check for new jobs in Switzerland? If you are actively applying, checking Jobs in Switzerland regularly during September 2026 can help you catch postings while they are still fresh. Broad location pages can change as employers add or remove openings, so revisit the listings and track which Switzerland jobs you have already reviewed. A simple application list can prevent duplicate applications and missed follow-ups. ### Apply to Jobs in Switzerland with Less Manual Work LiftmyCV uses AI matching, resume tailoring, and auto-apply tools to help you move through Switzerland job listings more efficiently.