JobCourier annunci per settore: Industria farmaceutica

​ Nous recherchons pour notre client spécialisé dans l'industrie chimique, un opérateur de production (H/F). ​ Vos responsabilités seront : - pratiquer des mélanges de poudre, de produits liquides et matières premières - régler les paramètres de certaines machines - s'assurer du bon fonctionnement des machines - réalisation de la production en suivant les procédures - respect des normes HSE (hygiène sécurité environnement) - Expérience professionnelle idéalement dans le secteur de l'industrie pharmaceutique, chimique ou agroalimentaire - Connaissance des bonnes pratiques de fabrication  - Connaissance SAP un atout - Français courant - Habitué au travail en équipe (2*8 / 3*8) ​ Si vous êtes intéressé(e) et correspondez au profil recherché, vous pouvez vous inscrire directement en transmettant votre dossier complet (CV - diplômes - certificat de travail).

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. ​ The perfect candidate: We are looking for a full stack software engineer to strengthen our software team within. In this challenging position, you will be a key member of the PCR HW Chapter, drive innovation and create added value for our customers in the area of healthcare Mol lab, Core lab and Point of care customer areas. This is a hands-on software development position where you define, build, test and release high-quality software for IVD and non-IVD products. As a domain expert, you will have a large influence on projects to enhance the future product portfolio. General Information: ? Start date: asap ? latest Start Date: 01.06.26 ? Planned duration: 12 months from start date ? Extension (in case of limitation): possible ? Workplace: Rotkreuz ? Workload: 100% ? Home Office: 50% remote Tasks & Responsibilities: ? You develop concepts and participate in feasibility studies to meet technical requirements. ? You perform and take ownership of specific software development tasks, ensuring reviews using checklists and templates. ? You lead work package definition, estimation, and planning, and enhance or document SW unit specifications and designs. ? You review designs and contribute to the SW architecture, defining quality attributes and staying updated with technology trends. ? You conduct root-cause analysis of complex issues and provide bug fixes for post-market software releases. ? You ensure compliance with processes, propose improvements, and stay informed about regulatory and market standards. Must Haves: ? University education in a software related field such as software or electrical engineering Industry experience ? Proven experience as a Software Engineer with a strong focus on Rust development.  ? Solid understanding of Rust's core concepts, including ownership, borrowing, and lifetimes.  ? Experience with asynchronous programming in Rust (e.g., using async/await).  ? Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).  ? Experience with Linux and Dockers  ? Basic scripting knowledge would be an advantage ? RabbitMQ knowledge would be an advantage ? Experience with CAN bus ? Event-Driven Architecture knowledge would be an advantage. ? First experience working in regulated environments such as the medical device industry. ? Highly motivated with focus on deadlines and a proactive and thorough way of working. ? Fluent in English and German is advantageous. ? Developers with an interest in interdisciplinary and hardware focussed. applications as well as electronic engineer with a strong backgrounds and interest in software development are encouraged to apply. ? Excellent communication and team working skills, flexibility, willingness to write good documentation and the drive to bring a product to its conclusion. Nice to Have: ? You have experience in agile environments ​ For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Are you interested in this opportunity? Kindly send us your CV today through the link in the advert.

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers ​ About the Team In a global, cross-functional environment, the PCR Software Development chapter is responsible for developing and maintaining integrated, unified, and reliable software solutions for Molecular Diagnostics Systems. By leveraging advanced capabilities, in-depth knowledge, and strong internal & external partnerships, the team drives accuracy, efficiency, and agility in innovating the Molecular Lab experience for customers and patients throughout their journey. As a Software Engineer working in Rust, you will be part of a cross-functional team playing a pivotal role in designing, developing, and maintaining software solutions. You will enable our Molecular Lab network to deliver accurate and timely diagnostic solutions, and your contributions will empower customers to make a real impact in patient care. Tasks & Responsibilities - Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical software. - Ensure the timely delivery of high-quality software for medical devices that meets both company standards and customer needs, influencing the success of the team and broader project outcomes. - Communicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teams. - Empower your team members to take ownership of their work, leading by example to foster teamwork and mentorship. Must Haves - Bachelor's degree or equivalent practical experience in a specialized field related to software development or engineering. - Several years of proven experience in software development, with demonstrated passion and hands-on professional experience working with Rust for at least two years, including: - Solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes). - Experience with asynchronous programming in Rust (e.g., async/await). - Familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx). - Hands-on experience with modern system architectures (e.g., event-driven architecture, DDD), quality-driven practices (TDD, BDD), or containerization technologies like Kubernetes is a plus. - Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis. - Excellent communication skills with the ability to foster an inclusive and diverse environment and collaborate effectively within and across teams. - Motivation to make an impact on team members, the company, customers, and patients. - Leads by example to foster cross-functional value delivery, establish a psychologically safe working environment, and empower the team while holding people accountable. - Experience as a Technical Lead within a team is a plus. - Certified ISAQB or equivalent is a plus. - English fluency is a must; German is a plus. ​ For this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Are you interested in this opportunity? Kindly send us your CV today through the link in the advert.

​ General Information: 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 stakeholders: 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 Experience in scheduling tool (Primavera) and operational readiness (manufacturing in GMP environment) needed Nice-to-Haves: Soft skills (e.g., strategic agility, feedback culture): comfortable 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 details 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

​ Bei Interesse und passender Qualifikation kannst du dich gerne direkt melden:  Alba Jansa alba.jansa(at)experis.ch +41 61 282 22 13 ​ Wir suchen einen erfahrenen Projektleiter (m/w/d) im Bereich Gebäudetechnik, der unser dynamisches Team in fester Anstellung verstärkt. In dieser Position haben Sie die Möglichkeit, vielfältige Projekte in der Pharma- und Life-Sciences-Branche an verschiedenen Standorten zu betreuen. DEIN PROFIL ? abgeschlossene Ausbildung und/oder Ausbildung/Weiterbildung als Techniker (HF)/Ingenieur (B.Sc/M.Sc.) der Gebäudetechnik ? Erfahrung als Projektleiter ? zuverlässig, kommunikativ und lösungsorientiert ? Teamplayer ​ UNSER ANGEBOT ? anspruchsvolle und interessante Projekte ? Mitgestaltung einer jungen Unternehmung ? moderne und gut ausgestattete Büroräumlichkeiten unmittelbar in Bahnhofsnähe ? junges und engagiertes Team ? flache Hierarchien und kurze Entscheidungswege ? jede Menge Freiheiten ? intensive Betreuung in Deiner Einarbeitungszeit ? ausgezeichnete Rahmenbedingungen  

Gi Group – Life Sciences Division is seeking a: Regulatory Affairs Associate The candidate will be placed, on a temporary contract through Gi Group, at an international pharmaceutical and biotech company focused on specialty medicinal products, to cover an extended absence. This position offers the opportunity to work in an international regulatory environment and contribute to the lifecycle management of medicinal products across multiple markets. This role is ideal for candidates with initial regulatory experience who want to strengthen their expertise in eCTD submissions and regulatory documentation management.   Key Responsibilities • Preparation and management of regulatory submissions in eCTD format • Compilation and organization of submission documentation and sequences • Support the Regulatory Affairs team in submission preparation and lifecycle activities • Maintenance of regulatory documentation and internal databases • Coordination of documentation for international regulatory submissions • Interaction with internal teams to collect and organize required regulatory data   Requirements • Degree in Life Sciences (Pharmacy, Biotechnology, Chemistry or related disciplines) • Initial experience in Regulatory Affairs within the pharmaceutical sector • Mandatory: familiarity with eCTD submission processes and regulatory documentation • Good knowledge of regulatory requirements for medicinal products • Professional English proficiency • Strong organizational skills and attention to detail   What we offer • Temporary contract via staffing agency • Opportunity to gain experience in an international pharmaceutical environment • Exposure to regulatory submission processes • Collaborative and supportive team environment   Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton and Bautech Personal. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 40 locations across Switzerland and over 200 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°. 

​ Für unseren Kunden, ein etabliertes Pharmaunternehmen im Raum Luzern, suchen wir per sofort eine/n engagierte/n Mitarbeiter/in Verpackung Pharma 100%. In dieser Position leisten Sie einen wichtigen Beitrag zur Herstellung und Bereitstellung von Arzneimitteln für klinische Studien und tragen so direkt zur Weiterentwicklung innovativer Therapien bei. ​ Ihre Aufgaben: Abfüllen, Etikettieren und Verpacken von Arzneimitteln für klinische Studien (manuell oder mit Maschinen) Bedienung und Überwachung von Verpackungsanlagen Dokumentation der Arbeitsschritte in Papierunterlagen und elektronischen Systemen (z. B. SAP) Einhaltung von Qualitäts- und Sicherheitsvorgaben (GMP) sowie sofortige Meldung von Auffälligkeiten Ihr Profil: Abgeschlossene Ausbildung in Pharmabranche oder Detailhandel Gute Deutschkenntnisse Genaue Arbeitsweise Teamfähigkeit ​ Interessiert? Bewerben Sie sich direkt über unser Online-Portal oder senden Sie mir Ihre Unterlagen per E-Mail.  Ich freue mich darauf, von Ihnen zu hören.

For one of our esteemed clients, international pharmaceutical and biotech company focused on specialty medicinal products, we are looking for a Regulatory Affairs Specialist to strengthen its Regulatory team. This position offers the opportunity to work in an international regulatory environment and contribute to the lifecycle management of medicinal products across multiple markets.   Key Responsibilities • Preparation and management of regulatory submissions in eCTD format • Lifecycle management activities including variations, renewals and maintenance of Marketing Authorisations • Preparation and review of regulatory documentation and product information (SmPC, PIL, labeling) • Coordination of submission dossiers for international markets • Interaction with internal departments (QA, CMC, Clinical, Pharmacovigilance) • Ensure compliance with international regulatory requirements • Management and compilation of eCTD sequences using regulatory publishing tools   Requirements • Degree in Life Sciences (Pharmacy, Biotechnology, Chemistry or related fields) • 4–5 years of experience in Regulatory Affairs within the pharmaceutical industry • Proven experience with medicinal products regulatory dossiers • Mandatory experience working with eCTD tools (experience with EXTEDO is highly preferred) • Hands-on experience with international submissions, variations and lifecycle management • Ability to work independently on regulatory documentation and product information • Professional English language proficiency   What the company offers • Permanent contract • Opportunity to work in an international pharmaceutical environment • Exposure to global regulatory activities • Hybrid work model (1 day per week remote work) • Collaborative and scientifically driven working environment   Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton and Bautech Personal. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 40 locations across Switzerland and over 200 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°. 

​ Für unseren Kunden in Werthenstein (LU) suchen wir eine engagierte und strukturierte Persönlichkeit als Produktionsplaner / Production Planner 100%. In dieser Schlüsselrolle übernehmen Sie die zentrale Koordination der täglichen Produktionsplanung und sorgen für einen reibungslosen Ablauf der Aktivitäten im Produktionsumfeld. Sie arbeiten eng mit verschiedenen Fachbereichen wie Operations, Process Engineering, Automation, Facility Engineering und weiteren Schnittstellen zusammen, um eine effiziente Planung, optimale Ressourcennutzung sowie eine hohe Prozessqualität im GMP-regulierten Umfeld sicherzustellen. ​ Ihre Aufgaben - Sie fungieren als zentrale Ansprechperson für das tägliche Management des Produktionsplans (Finite Schedule) und koordinieren Aktivitäten auf dem Shopfloor sowie im Anlagenbetrieb. - Sie koordinieren die Zusammenarbeit zwischen Operations, Process Engineering, Automation, Facility Engineering, Microbiology sowie weiteren relevanten Funktionen, um die Aktivitäten im Prozessbereich zu steuern. - Sie aktualisieren und pflegen den Produktionsplan täglich. - Sie stellen die Abstimmung zwischen dem Site Plan of Record und dem Finite Schedule sicher, um Konsistenz und Genauigkeit zu gewährleisten. - Enge Zusammenarbeit mit Technology Transfer, um Szenarien für neue Produkteinführungen zu planen und zukünftige Aktivitäten proaktiv zu koordinieren. - Sicherstellung der reibungslosen Durchführung von Aktivitäten in den Bereichen Manufacturing, Process Engineering, Plant Engineering, Kalibrierung, Labor und Warehouse Operations. - Zusammenarbeit mit Netzwerkexpert:innen zur Entwicklung einer Roadmap zur vollständigen Implementierung der RTMS-Funktionalität, um die Kapazitätsauslastung der Anlage und die Ressourcenzuweisung zu optimieren. - Aufbau und Weiterentwicklung von RTMS-Betriebsmodellen für Fed-Batch- und Continuous-Manufacturing-Prozesse. - Funktionsübergreifende Zusammenarbeit zur Durchführung von Debottlenecking-Analysen sowie Unterstützung von Manufacturing Technology und Strategy bei Kapazitätsausbau- und Auslastungsstrategien. - Unterstützung bei der Bewertung unvorhergesehener Ereignisse im Produktionsplan sowie Entwicklung geeigneter Mitigationsmassnahmen. - Verantwortung für die Einhaltung des Produktionsplans, inklusive Eskalation bei Problemen sowie Sicherstellung einer optimalen Ressourcenauslastung der Produktions- und Anlagenteams. Ihr Profil - Ausbildung oder Studium in einer relevanten Fachrichtung. - Mindestens 2?5 Jahre Berufserfahrung in der Herstellung von Biologika unter GMP-Bedingungen, idealerweise im Bereich Upstream oder Downstream Processing. - Analytische und lösungsorientierte Denkweise mit der Fähigkeit, bestehende Lösungen aus neuen Perspektiven zu betrachten. - Hohe Lernbereitschaft sowie Motivation zur kontinuierlichen Verbesserung und Weiterentwicklung. - Fähigkeit, auch unter Druck in einem komplexen GMP-Umfeld effizient zu arbeiten. - Sehr gute Englischkenntnisse sowie gute Deutschkenntnisse: Englisch: C1 (mündlich und schriftlich) und Deutsch: B2 (mündlich und schriftlich) ​ Wenn Sie Erfahrung in der Herstellung von Biologika mitbringen, gerne funktionsübergreifend arbeiten und Freude daran haben, komplexe Abläufe zu koordinieren und kontinuierlich zu verbessern, bietet diese Position eine spannende Möglichkeit, Ihr Know-how in einem dynamischen und innovativen Umfeld einzubringen. Wir freuen uns auf Ihre Bewerbung.

​ Für unseren Kunden, ein etabliertes Pharmaunternehmen im Raum Luzern, suchen wir per sofort eine/n engagierte/n Mitarbeiter/in Verpackung Pharma 100%. In dieser Position leisten Sie einen wichtigen Beitrag zur Herstellung und Bereitstellung von Arzneimitteln für klinische Studien und tragen so direkt zur Weiterentwicklung innovativer Therapien bei. ​ Ihre Aufgaben: Abfüllen, Etikettieren und Verpacken von Arzneimitteln für klinische Studien (manuell oder mit Maschinen) Bedienung und Überwachung von Verpackungsanlagen Dokumentation der Arbeitsschritte in Papierunterlagen und elektronischen Systemen (z. B. SAP) Einhaltung von Qualitäts- und Sicherheitsvorgaben (GMP) sowie sofortige Meldung von Auffälligkeiten Ihr Profil: Abgeschlossene Ausbildung in Pharmabranche oder Detailhandel Gute Deutschkenntnisse Genaue Arbeitsweise Teamfähigkeit ​ Interessiert? Bewerben Sie sich direkt über unser Online-Portal oder senden Sie mir Ihre Unterlagen per E-Mail. Für Fragen stehe ich Ihnen selbstverständlich gerne zur Verfügung: Ich freue mich darauf, von Ihnen zu hören.

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. ​ Background The candidate will develop Instrument Control software, Service software and Instrument Management SW for the Cobas 6800/8800/5800 instruments. The Instrument Control software is real-time in nature and is developed in C++ using an existing real-time framework with low-level hardware drivers and is tested using both real and simulated hardware and it is Event-Driven Architecture. The perfect candidate It is of critical importance that the candidate has primarily worked with modern C++ (C++11 or newer) over the past 2 to 5 years, including in their most recent or current project. Furthermore, it is essential that Linux has been used as the primary development operating system during the past 2 to 5 years, including in the candidate's latest or current project. In addition, the candidate should have gained experience working within small to large development teams during the past 2 to 5 years, as we are specifically seeking a strong team player rather than an individual contributor. General Information ? Start date: asap ? latest Start Date: 01.06.26 ? Planned duration: 12 months from start date ? Extension (in case of limitation): possible ? Workplace: Rotkreuz ? Workload: 100% ? Home Office: 50% remote ? Team: 8?10 Tasks & Responsibilities ? Proactive participation in all phases of software development from feasibility studies through design, development, testing and bug fixing and maintenance ? Collaboration within the Scrum-Teams ? Independent interaction with internal framework manufacturers ? Based on requirements and models, definition of software architecture, design and specifications, ultimately leading to implementation ? Participation in the definition of work packages, their estimation and planning in a sprint-based agile environment ? Adherence to a software development process including contribution to written deliverables and documentation Must Haves ? Min. Bachelor degree in a software related field such as software or electrical engineering or similar (****) ? Min. 5+ years of hands-on experience as Software Engineer, preferred in the regulated environment such as the medical device industry (****) ? Min. 3?5 years hands-on experience with C++ and Linux from the last project or position (****) ? Strong with Linux Dockers (****) ? Experience with CAN bus (****) ? Fluent in English (spoken and written) ? Highly motivated with focus on deadlines and a proactive and thorough way of working ? Ability to work within a team and still be proactive ? Ability to work within agile and Scrum Teams ? Software architecture would be a big plus Nice to Have ? Event-Driven Architecture knowledge ? SAFe certification ? Scrum experience ? Basic scripting knowledge ? RabbitMQ knowledge ? German is advantageous ​ If you are interested to apply, please send us your CV. This job will halt to accept applications on 13.03.2026 Interviews will take place from the end of March 2026, 2 rounds planned.  

​ Mandaté par notre client spécialisé dans le domaine de la stérilisation sur le Canton de Vaud, nous sommes activement à la recherche d'un(-e) Assistant(-e) technique en stérilisation.   ​ Votre mission : Au sein d'une structure experte dans le domaine de la stérilisation, vous jouez un rôle central dans la gestion opérationnelle et la qualité des prestations délivrées. À ce titre, vous serez amené(-e) à : - Coordonner et sécuriser les flux de transport ainsi que la circulation des analyses entre les différents sites clients - Veiller à la mise à disposition, dans les délais définis, de dispositifs stériles conformes et opérationnels pour l'ensemble des services et partenaires - Accompagner et sensibiliser les équipes aux bonnes pratiques et aux exigences liées à la stérilisation - Apporter votre expertise en matière de retraitement des dispositifs médicaux et agir comme interlocuteur(-trice) de référence auprès des services internes et des structures externes - Gérer les flux logistiques liés aux lits, au linge, aux tenues professionnelles ainsi qu'à l'organisation des vestiaires Votre profil : - Expérience dans le domaine de la stérilisation et du lavage - Sens des responsabilités et respect strict des procédures - Rigueur, organisation et esprit d'équipe - Bonne capacité de communication et aisance dans la transmission d'informations - Capacité à travailler dans un environnement exigeant et structuré ​ Cliquer sur le bouton en ligne pour postuler en toute simplicité. Nous nous réjouissons de recevoir votre candidature et prendrons contact avec vous dans les plus brefs délais.

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers.   ​ On behalf of our global Pharmaceutical client based in Basel, we are looking for a technically strong data professional with solid experience in data engineering, data warehousing, and database management, including hands-on expertise with NoSQL databases such as MongoDB. Strong Python scripting skills and practical experience with ETL orchestration tools are essential. The ideal candidate has a good understanding of Text Analytics, Text and Data Mining (TDM), and Large Language Models (LLMs), and is familiar with applying FAIR principles in data workflows. Experience with scientific or other text-based data, high-performance computing environments, and API development (e.g., GraphQL) is highly desirable. A biomedical background is a plus. General Information: ? Start Date: asap ? Latest Possible Start Date: 01.06.2026 ? Planned Duration of Employment: 12 months ? Extension (for temporary contracts): Likely if budget gets approved ? Workplace: Basel ? Workload: 100% ? Home Office: partially possible Tasks & Responsibilities: ? Designing and implementing the ETL pipeline and MongoDB scheme. ? Managing the document database, data curation, and FAIRification (cleaning, parsing, disambiguation, deduplication, data harmonization etc.), including ongoing database maintenance. ? Integrating new data sources, including the development of robust parsers and text cleaning workflows. ? Enhancing the user experience (e.g., building a data warehouse and APIs). ? User support for utilizing RoMine datasets (documentation, training, use case support). Must Haves: ? Data engineering, data warehousing, and database experience  ? Experience with NoSQL/MongoDB database.  ? Good understanding in the area of Text Analytics/Mining, TDM, and LLMs. ? Experience or knowledge of ETL orchestration tools, such as Airflow.  ? Strong proficiency in Python scripting. ? Knowledgeable on the FAIR principles and associated methodology. ? Familiarity with scientific literature/published content/literature or/and other text-based data ? Excellent communication and interpersonal skills in English (fluent), German is nice to have. ? Interdisciplinary teamwork, ability to explain technical concepts to non technical stakeholders ? Exposure to high-performance computing environments. ? Experience with API development (e.g., GraphQL API) is a plus. ? Biomedical background/education is a plus ​ If you are interested in this opportunity, please apply with a copy of your CV or feel free to reach me at +41 61 282 2223

​ Welcome to a leading company in the pharmaceutical manufacturing industry, recognized for its commitment to quality, compliance, and operational excellence. We offer you the opportunity to work in a highly regulated and professional environment where your expertise is valued and your attention to detail makes a real impact on patient safety and product quality. Our organization places strong emphasis on GMP standards, teamwork, and continuous improvement. You will collaborate closely with cross-functional teams to ensure timely and compliant batch release while contributing to a culture built on precision, accountability, and open communication. Join our dedicated team in Visp and help ensure the highest standards in pharmaceutical manufacturing. ​ Description Making sure the batch was made properly, according to procedure and regulatory requirements. Reviewers should have great attention to detail, be able to work independently, and have a thorough knowledge of the manufacturing process they are reviewing. Tasks - Review paperbased executed batch records within the specified timeframe. - Track, report and monitor batch record review and other relevant critical metrics to ensure on-time batch release. - Raise meetings with Ops related observations in a timely manner. Skills - Professional experience in GMP production environment, quality procedures and SOP execution and/or Bachelor's/Master's Degree or equivalent experience. - Preferred area of study: Pharmaceutical Technology, Biotechnology, Chemistry, Pharmacy or equivalent scientific degree. - Experience in batch record review is highly preferred. - GMP experience (min. 2 years) - Great communication skills Additional Information - On-Site in Visp (no home office) ? Paper based - Business fluent German is a MUST - English preferred ​ Due to Swiss Employment regulations, for this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Interested? I look forward to receiving your application!

​ Background: The assignment will be for the Computational Sciences Center of Excellence (CS-CoE) organization of a leading Pharmaceutical company in Basel. They are conducting the award-winning ?Target Evaluator? project, in close collaboration with colleagues from Translational Medicine Neuroscience, focusing on the implementation of the requirements from the project. The project is integrating select open-source multi-agent systems towards a comprehensive, unbiased ranking framework for new target proposals. The perfect candidate: We are looking for someone with a Bachelor's or Master's degree in Computer Science, Engineering, Information Systems, Bioinformatics, or equivalent professional experience. The ideal candidate has 5+ years of Python programming, 3+ years of REST API design experience, and excellent English communication skills. The perfect candidate is proactive, analytical, highly adaptable, and thrive in cross-functional teams, quickly learning new technologies to tackle complex technical challenges. General Information: ? Start date: asap ? latest Start Date: 1.5.2026 ? Planned duration: 31.12.2026 ? Extension (in case of limitation): possible ? Workplace: Basel ? Workload: 100% ? Home Office: 2 days max. remote Tasks & Responsibilities: ? Provide agile software development services for the ?Target Evaluator? project according to the project plan. ? Provide technical consulting services to support the project team. ? Develop and implement robust backend functionalities that meet defined business needs ? Design and implement APIs for the "Target Evaluator" ? Integrate with other applications, working out technical details independently with other teams ? Research and apply new data processing and analysis techniques ? Improve quality through performance evaluation, implementation of testing strategies, and tooling Must Haves: ? Bachelor/Master degree in a relevant field such as Computer Science, Computer Engineering, Mathematical Engineering, Information Systems, or Bioinformatics is preferred. Candidates with extensive professional experience in the field can also be considered. ? Python programming (5+ years) ? Experience in REST API design (3+ years) ? Some experience in ML engineering in e.g. life sciences ? Experience in CI/CD using GitLab ? Experience in GitOps ? Experience in Kubernetes for hosting of services ? Experience in implementing user interfaces ? Working in HPC environments ? Knowledge of LLMs and LLM-based multi agent frameworks ? Excellent communication skills in fluent English, both written and verbal ? Strong collaborative approach and a desire to work effectively within a cross-functional team environment. ? Proactive and analytical mindset for identifying, troubleshooting, and resolving complex technical issues. ? High adaptability and a commitment to quickly learning new technologies and methodologies to meet evolving project needs and priorities.   ​ If you are interested, please rea y ​ Due to Swiss Employment regulations, for this position we can only consider applicants with a Swiss work permit or a Swiss/EU passport. Interested? I look forward to receiving your application!