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.

​ 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.

​ Administrative Assistant I Our innovative and leading company in the field of biopharmaceutical research and development is committed to improving global health and quality of life. With cutting-edge technology and a strong focus on the personal development of our employees, we create a dynamic work environment where teamwork, dedication, and expertise are highly valued. Become part of our committed team in Visp and actively contribute to the development of groundbreaking therapies. ​ Your Tasks and Responsibilities Review and transfer of reserve, shipping, and stability samples Review of retention samples Issuance of reserve and stability samples Storage of retention samples in accordance with regulations Ensuring compliance with quality (SOP and GMP) and safety guidelines Support with documentation and reporting in the administrative area Communication with QC project managers, shift teams, logistics, and QA Processing and responding to correspondence, including confidential information Required Skills and Qualifications Completed training in administration or a comparable qualification 1–3 years of professional experience in an administrative environment, ideally in the pharmaceutical or biotech industry Good knowledge of GMP and SOP guidelines Excellent organizational skills and strong attention to detail Strong communication skills in German and English; knowledge of French is an advantage Proficiency with MS Office (Word, Excel, Outlook) Ability to handle sensitive information confidentially Team player with flexibility ​ Your Opportunity If you are a dedicated individual who enjoys working in an innovative environment and wants to actively contribute to meaningful research projects, we look forward to receiving your application. Join our dynamic team in Visp and help shape the future of biopharmaceutical innovation!