Experis

​ 5+ ans en développement Python, idéalement dans un environnement trading ou finance de marché ​ Tu rejoindras une équipe agile au cœur des opérations de trading, avec pour mission de : Concevoir, développer et maintenir des outils Python pour le Front Office (pricing, risk, monitoring, automation…) Collaborer étroitement avec les traders, quants et analystes pour comprendre leurs besoins et proposer des solutions efficaces Optimiser les performances des scripts et des flux de données en temps réel Participer à l’amélioration continue de notre stack technique et de nos pratiques de développement Compétences clés Techniques Maîtrise de Python (structuration, performance, testing) Solide expérience avec Pandas , NumPy , SQL Connaissance des environnements Linux , Git , Docker Expérience dans le trading algorithmique , les systèmes de pricing , ou les plateformes de données financières Bonus : FastAPI , Kafka , AWS , CI/CD , C++ , JavaScript ​ Contacte nous : Antoine Wormser - 022 818 87 78

​ Join a leading global pharmaceutical company dedicated to improving patient outcomes through innovative drug development and manufacturing. Renowned for its commitment to quality, sustainability, and cutting-edge technology, this organization offers a dynamic and collaborative environment where your expertise can make a meaningful impact. Located in the picturesque region of Visp, Switzerland, the company provides an inspiring setting for professional growth and development within the pharmaceutical industry. ​ Description: Key responsibilities: Lead technical expansion and capacity increase projects within Drug Product manufacturing to support production ramp-up. Provide technical input to project design, ensuring compliance with operational needs and regulatory standards (e.g., EU GMP Annex 1). Coordinate cross-functional teams and external suppliers, manage project governance, and ensure delivery on time and within scope. Develop and implement best-practice processes aligned with current industry and regulatory trends. Manage change control, troubleshooting, and deviations related to projects and equipment. Establish and update operational procedures in collaboration with manufacturing and quality functions. Key requirements: Extensive technical experience in GMP manufacturing (Drug Product experience preferred). Proven track record of project coordination/management within pharmaceutical manufacturing. Experience with CAPEX projects and equipment qualification is an advantage. In-depth knowledge of cGMP and Annex 1 requirements. Fluent in English, german is a plus Highly collaborative, results-driven, and with excellent interpersonal and communication skills. Agile mindset with ability to deliver under pressure and changing priorities. min. 2 years experience no home-office ​ If you believe you are the perfect fit for the role and you are interested, do not hesitate to call or email me directly.

​ General Information: Start date / Latest possible start date: 2nd of January / mid of January Planned duration / Extension option: 1 year and expected to be extended every year Workplace & remote work possibilities: Visp site PCP building - Remote 2-3 days Workload: 100 % Tasks & Responsibilities: Clear description of responsibilities: owning the E2E schedules for programs (Operational readiness) including workload, updating the resources workload for PCP operation (manufacturing building in Visp) , Lead the meeting with internal stakeholders (QA, QC, Ops, MSAT, Plant. Eng, support team,...) for E2E schedule update and tracking Project background / context: support/own the planification of the different projects (operational readiness NOT CAPEX) and support others tasks not only related to scheduling Key internal and external stakeholders: No external stakeholders only internal (Lonza and especially PCP team) Must-Haves: Years of relevant industry experience: 5 years minimum Specific tools/systems (e.g., Primavera P6): full autonomy P6 and good practice on excel Mindset or working style (e.g., data-driven) open mindset, curious on data, develop schedule on primavera and excel Nice-to-Haves: Soft skills (e.g., strategic agility, feedback culture): confortable in challenging people, pro-active, lead meeting for building schedule and execution, knowledge of pharmaceutical environment is a plus (operation/manufacturing) Project methodology / leadership experience: Leadership to support the team to build a realistic schedule, need to have a good methodology knowledge, able to accept to go in the detailes schedule at tasks level as needed ​ Tasks & Responsibilities: Clear description of responsibilities: owning the E2E schedules for programs (Operational readiness) including workload, updating the resources workload for PCP operation (manufacturing building in Visp) , Lead the meeting with internal stakeholders (QA, QC, Ops, MSAT, Plant. Eng, support team,...) for E2E schedule update and tracking Project background / context: support/own the planification of the different projects (operational readiness NOT CAPEX) and support others tasks not only related to scheduling Key internal and external stakeholders: No external stakeholders only internal (Lonza and especially PCP team) Must-Haves: Years of relevant industry experience: 5 years minimum Specific tools/systems (e.g., Primavera P6): full autonomy P6 and good practice on excel Mindset or working style (e.g., data-driven) open mindset, curious on data, develop schedule on primavera and excel Nice-to-Haves: Soft skills (e.g., strategic agility, feedback culture): confortable in challenging people, pro-active, lead meeting for building schedule and execution, knowledge of pharmaceutical environment is a plus (operation/manufacturing) Project methodology / leadership experience: Leadership to support the team to build a realistic schedule, need to have a good methodology knowledge, able to accept to go in the detailes schedule at tasks level as needed ​ If you are interested and believe you are a great fit, do not hesitate to contact me directly: alba.jansa(at)experis.ch +41 61 282 22 13

​ Looking for a motivated Scientist for one of our clients based in Visp. ​ Description: Tätigkeitsbeschreibung Technical representation of the QC Microbiology department (Visp, Lonza) internally and at customer meetings/audits/visits as well as during inspections within the projects assigned to him Scientific SME for project-specific analyses and other microbial analyses in QC Microbiology: Monitoring, evaluating and, if necessary, coordinating the implementation of current improvements. Coordinating and ensuring the timely completion of individual work packages assigned to specific business units (BUs), while facilitating effective communication within interdisciplinary overarching teams (e.g., studies, validation/verification, deviations, and transfers). Min. 2 years experience max 2 days remote (100 % on-site preferred) German preferred ​ If you are interested and believe you can be a good fit, do not hesitate to contact me directly: Alba Jansa: +41 61 282 22 13 alba.jansa(at)experis.ch

​ For one of our pharma clients based in Visp, we are looking for a Warehouse Operator . ​ Description: Tracks shipments and receives, processes, stores, and distributes material, tools, equipment, and products within establishments.Inspects products for damages and reports as needed.Reads production schedules, customer orders, work orders, shipping orders, or requisitions to determine items to be moved, gathered, or distributed.Conveys materials and items from receiving or production areas to storage or to other designated areas by hand, hand truck, or electric hand truck. Experience in logistics, tugger trains and forklifts desired German speaking mandatory no remote work available ​ If you are interested and believe you can be a good fit, do not hesitate to apply or contact me directly.

​ The Administrative CapEx Project Assistant will support the successful execution of a capital expenditure (CapEx) project in a biopharmaceutical manufacturing environment. The role involves providing administrative and organizational support across all phases of the project, from conceptual design through to performance qualification (PQ), including GMP-compliant change management, vendor coordination, and team onboarding/offboarding. The position ensures efficient project documentation, compliance, and communication while assisting the Project Manager and team in maintaining the project’s timelines and deliverables. ​ Key Responsibilities Project Administration & Coordination Serve as the central point of contact for project-related administrative matters. Plan, schedule, and coordinate project meetings, workshops, and reviews. Prepare, distribute, and archive meeting minutes and action item lists. Support project onboarding/offboarding processes for internal and external team members (badge requests, IT access, training coordination, workspace setup, etc.). Manage seat planning and workspace allocation for project staff and contractors. Contractor & Vendor Onboarding Support Coordinate onboarding of EPCM and other external contractors (access requests, NDA processing, training completion tracking). Maintain up-to-date contractor lists, role assignments, and contact directories. Ensure contractors meet site-specific compliance and safety requirements prior to mobilization. Documentation & Workflow Management Maintain and organize project documentation in alignment with company and GMP documentation standards. Initiate and track document workflows (e.g., via DocuSign or internal systems). Support document control activities, including version tracking, signature routing, and controlled storage. Liaise with Quality and Document Control departments to ensure adherence to applicable procedures. Procurement & Financial Administration Create and track purchase requisitions, purchase orders, and invoice approvals in collaboration with procurement and finance teams. Support budget tracking from an administrative standpoint (no financial ownership). Maintain an overview of supplier and service contract documentation. Training & Compliance Administration Coordinate and track completion of required GMP and EHS trainings for internal and external team members. Support preparation of documentation for internal project reviews (and audits or inspections, if applicable). Communication & Reporting Support Maintain project communication channels and distribution lists. Support preparation of project communication materials, status reports, or presentations as requested. Assist in coordinating travel, visitor management, and on-site logistics for project-related activities. Qualifications: Education & Experience: Commercial or administrative education (e.g., office management, business administration, project coordination) or equivalent experience. Proven experience in an administrative or project coordination role, ideally within a GMP-regulated, biopharmaceutical, or technical project environment. Skills & Competencies: Excellent organizational and coordination skills with high attention to detail. Strong communication skills and service-oriented mindset. Proficiency in MS Office Suite (Word, Excel, PowerPoint, Outlook); experience with SAP, DocuSign, or similar systems advantageous. Ability to handle multiple priorities and deadlines in a dynamic project environment. Discretion in handling confidential information. Personal Attributes: Reliable, structured, and proactive working style. Collaborative and supportive team player. Comfortable working with both technical and non-technical stakeholders. Languages: Fluent in German and English, both written and spoken. Work Environment Collaboration with cross-functional teams (Engineering, QA, Operations, HR, EHS, Procurement). Exposure to a dynamic, fast-paced project environment with external contractors and partners on-site. ​ if you are interested and believe you are a good fit, do not hesitate to contact me directly.

​ Join a leading biopharmaceutical company dedicated to advancing healthcare through innovative bioprocessing solutions. Our state-of-the-art facilities in Visp, Switzerland, are at the forefront of biotechnological research and manufacturing, offering a dynamic and collaborative environment. We are committed to sustainability, excellence, and continuous improvement, providing our employees with opportunities for professional growth and impactful work in the life sciences sector. ​ Description: Develops, enhances, and implements systems that increase efficiency and optimize all phases of service or production processes, from design to manufacturing. Oversees process design projects, and ensures the efficient and safe functioning of all the processes related to producing a product, substance, or service. Designs processes and equipment related to the development and commercialization of products or services that are cost effective and in keeping with a given budget. Evaluates existing processes, suggests measures for improvement, and configures manufacturing systems to reduce cost, improve sustainability, boost productivity, quality, and profitability, and develop best practices within the production process. Implements methods and process designs, creates prototypes, tests, and makes necessary modifications where required. 3-5 Years Experience Language: English required / German a plus ​ If you are interested and believe you are a good fit, do not hesitate to contact me directly: alba.jansa(at)experis.ch +41 61 282 22 13