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    Reference number: 850276/1

    Production Operator (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Perform production tasks across facilities while ensuring compliance with safety regulations and cGMP quality standards
    • Identify, interpret, and resolve deviations in production processes to maintain efficiency and quality
    • Execute production steps with precision, including documentation, calculations, and reporting
    • Support onboarding and training of new team members to strengthen team knowledge and performance
    Online since: Fri Nov 21 14:56:39 CET 2025
    Reference number: 850280/1

    Scientist (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Technical representation of QC Microbiology during internal reviews, customer meetings, audits, site visits, and inspections
    • Scientific SME support for project-specific microbial analyses, including monitoring, evaluating, and coordinating the implementation of improvements
    • Coordination of work packages assigned to business units (BUs), ensuring timely completion and alignment with project objectives
    • Facilitation of communication across interdisciplinary teams (e.g., studies, validation/verification, deviations, transfers)
    • Continuous improvement of QC Microbiology processes in line with regulatory standards and industry best practices
    Online since: Fri Nov 21 14:55:16 CET 2025
    Reference number: 850273/1

    QA CSV Specialist (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Act as QA liaison: Represent the QA department and serve as the primary contact for CSV-related matters with internal and external stakeholders
    • Ensure compliance: Monitor evolving industry regulations (GMP Annex 11, 21 CFR Part 11, GAMP, PIC/S) and integrate best practices into local policies and procedures
    • System validation: Oversee validation and lifecycle management of computerized systems (MES, Delta V, spreadsheets, bench-top equipment)
    • Technical guidance: Provide expert IT input to support GMP decisions on system validation and lifecycle management
    • Continuous improvement: Develop and implement procedures, Validation Plans, and Master Plans to enhance efficiency and compliance
    • Project leadership: Define scope, create implementation plans, track progress, and proactively address risks to keep projects on schedule
    • Auditing: Conduct audits to ensure validation activities meet regulatory and corporate standards
    • Cross-functional collaboration: Partner with engineering, automation, and operations to assess new applications and define validation requirements
    • Escalation support: Act on behalf of the QA CSV Manager to ensure timely resolution of GMP issues
    Online since: Fri Nov 21 14:54:09 CET 2025
    Reference number: 850650/1

    Administrative Assistant (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Provide administrative support to the organization or department, ensuring smooth daily operations
    • Assist management with tasks such as tracking, compiling, and organizing information of interest
    • Prepare and maintain reports that summarize administrative activities and key data
    • Manage correspondence by reading, drafting, and responding to emails, letters, and other communications
    • Handle confidential information with discretion and professionalism
    • Coordinate schedules and meetings, including logistics and documentation when required
    • Support process improvements by identifying opportunities to streamline administrative workflows
    Online since: Fri Nov 21 14:36:48 CET 2025
    Reference number: 850373/1

    CTA/ Senior CTA (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Support daily operational and administrative activities in a global Phase 3 study
    • ETMF management (Veeva), document filing and document review 
    • Contribution to study clean-up activities
    • Oversight of two CROs, including insurance tracking and review of study plans and documentation
    • Coordination with internal stakeholders and external partners
    • Ensuring structured workflows, prioritization and efficiency in a fast-paced environment
    • Support ongoing process improvements and organizational tasks
    • Close collaboration with the Study Lead and the broader study team
    Online since: Fri Nov 21 14:19:39 CET 2025
    Reference number: 850638/1

    Quality Inspector (m/f/d)

    Freelance/temporary employment for a project
    Villeneuve / Bulle / Martigny
    • Verifying the compliance of production processes and critical operations (crimping, stripping, assembly).
    • Perform visual and dimensional inspections
    • Use measuring tools (caliper, micrometer, optical systems)
    • Check the electrical and electronic characteristics of components
    • Apply quality procedures and technical instructions
    • Ensure the traceability of checks in the quality system
    • Collaborate with production, maintenance and engineering teams to resolve issues
    • Actively participate in customer inspections and quality events.
    Online since: Fri Nov 21 14:15:55 CET 2025
    Reference number: 850634/1

    Ingenieur Qualitätssicherung (m/f/d)

    Freelance/temporary employment for a project
    Villeneuve / Bulle / Martigny
    • Implementing and monitoring quality processes to ensure product and operational compliance
    • Participating in internal and external audits, as well as customer inspections
    • Leading quality meetings with multidisciplinary teams to improve performance and reduce risks
    • Deploying and maintaining quality tools (PFMEA, SPC, control plan)
    • Performing statistical analyses and quality reports
    • Ensuring production processes comply with ISO 9001 standards and customer requirements
    • Participate in continuous improvement projects (Lean, Six Sigma)
    • Collaborate with production, maintenance, R&D and supply chain teams
    • Contribute to operator training on quality standards.
    Online since: Fri Nov 21 13:50:15 CET 2025
    Reference number: 849910/1

    Clinical Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Analyse and interpret clinical data in collaboration with Biostatistics and Data Management
    • Robust experience in data review and data cleaning to ensure data quality and data integrity
    • Scientific support in the conduct and evaluation of clinical trials (phase II-III) with a focus on rare diseases
    • Preparation and review of study documents (e.g. protocols, IBs, CSRs)
    • Close collaboration with interdisciplinary teams as part of the study management team (Clin Ops, DM, Stats, Regulatory Affairs, etc.)
    • Support in communication with trial sites, CROs and authorities
    • Contribute to the development of internal and external presentations
    Online since: Fri Nov 21 13:17:32 CET 2025
    Reference number: 850124/1

    Medical Device Clinical Safety Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Provide expert oversight and leadership for all clinical safety and vigilance activities for Class II and/or III Medical Devices (MD), ensuring compliance with global regulations and internal standards throughout the product lifecycle
    • Manage and execute the MD vigilance process, including the intake, processing, assessment, and reporting of adverse events, ensuring timely and compliant submissions to regulatory authorities
    • Review of core Medical Device study documentation to ensure robust inclusion of safety-related content. This includes, but is not limited to, the Clinical Investigation Plan (CIP/Protocol) and the Investigator’s Brochure (IB)
    • Develop and maintain the Reference Safety Information (RSI) for clinical investigations, ensuring its accuracy, proper dissemination, and timely updates based on emerging safety data
    • Conduct and/or contribute significantly to Medical Device benefit-risk assessments, providing expert interpretation of clinical safety data to inform regulatory and business decisions
    • Ensure the practical application and integration of MD risk management principles within clinical safety processes, aligning activities with the requirements of ISO 14971 (Medical devices – Application of risk management to medical devices)
    • Serve as the subject matter expert for all safety-related activities within MD clinical investigations
    • Maintain an expert-level understanding and ability to practically apply the principles of ISO 14155:2020 (Clinical investigation of medical devices for human subjects – Good clinical practice) to the design, conduct, monitoring, recording, and reporting of clinical investigations, specifically concerning safety reporting and subject protection
    • Provide guidance to clinical teams, investigators, and site staff on clinical investigation safety requirements, particularly those outlined in ISO 14155
    Online since: Wed Nov 19 15:19:37 CET 2025
    Reference number: 849929/1

    Legal Consultant (m/f/d)

    Freelance/temporary employment for a project
    Geneva
    • Provide legal analysis and advice on HR policies, rules and procedures
    • Support employment-related grievances, internal appeals and cases before the ILOAT
    • Advise on processes such as probation, performance management, misconduct investigations, disciplinary actions, separations and organizational restructuring
    • Handle matters related to medical leave, prolonged sick leave, data protection and ethics compliance
    • Deliver cross-functional legal support for decision-making, compliance, risk management and negotiations
    Online since: Wed Nov 19 10:30:42 CET 2025

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    Reference number: 849919/1

    Supply Chain Project Planner (m/f/d)

    Freelance/temporary employment for a project
    Lucerne
    • Represent the E2E Supply Chain organization in cross-functional disentanglement meetings
    • Maintain close alignment with E2E planners across all impacted product groups
    • Coordinate and influence stakeholders across multiple regions and business units
    • Develop 36-month supply plans for Finished Goods, Bulk, and API
    • Ensure structured escalation management and adherence to Tier processes
    • Represent the product portfolio in Site Supply Reviews, Global Supply Reviews, and Demand Reviews
    • Manage allocations in situations of supply–demand imbalance
    • Monitor inventory levels, report risks, and manage discard processes
    • Identify opportunities for supply chain optimization across the portfolio
    • Contribute to profit planning, volume planning, and network transfer activities
    • Drive product lifecycle activities, including launches and discontinuations
    Online since: Tue Nov 18 13:28:54 CET 2025
    Reference number: 849831/1

    Lab Technician (m/f/d)

    Freelance/temporary employment for a project
    Hinwil
    • Hands-on job in the laboratory
    • Preparation of test devices
    • Execution of measurement campaigns with data acquisition
    • Validation of measurements and data / data analysis
    • Reliability and structured mode of working are essential
    Online since: Tue Nov 18 10:48:18 CET 2025
    Reference number: 849390/1

    Building Safety Officer (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Monitor and ensure compliance with legal regulations, standards, and internal guidelines for building safety
    • Conduct regular safety inspections and risk assessments across buildings and facilities
    • Coordinate and oversee fire safety, occupational safety, and evacuation drills
    • Prepare and maintain safety documentation, inspection reports, and risk assessments
    • Collaborate with internal departments, external authorities, and service providers to implement safety measures
    • Advise managers and employees on safety-related topics and best practices
    • Initiate and monitor corrective actions for identified deficiencies
    • Support construction and renovation projects by ensuring safety requirements are met
    Online since: Fri Nov 14 15:08:23 CET 2025
    Reference number: 849367/1

    Technical Lead Drivetrain Development (m/f/d)

    Freelance/temporary employment for a project
    Hinwil
    • Design, development and optimization of drive trains for actuators
    • Technical interdisciplinary coordination of internal specialists in transmissions, motor technology, power- and motion control
    • Regular exchange and close cooperation with the development adjacent teams (e.g. requirements, verification)
    Online since: Fri Nov 14 13:35:20 CET 2025
    Reference number: 848980/1

    Data Engineer Mainframe Db2 z/OS DBA (m/f/d)

    Ticino
    • Support Db2 Environments; Integrate external vendor products and interfaces into the Mainframe landscape;Establish recovery routines for infrastructure and business data using products suites from IBM and BMC; Assist and advise database object design to business applications.
    • Design models and templates to provide best practices in data migration efforts.
    • Review logical models and provide physical database designs in support of Business initiatives.
    • Database object installations across all application landscapes (Development, QA, Production).
    • SQL performance reviews and approvals for all application release packages utilizing Changeman Approvals line-item sign-off.
    • Incident and Problem Management related to Db2 usage for Business applications and Operations.
    • Identify and introduce new Db2 functions to Business applications for possible integration into their respective mainframe software environments.
    • Support the implementation of Db2 Certificate-based security for technical accounts connecting to Db2 environments (QA and Production).
    • Implement and support ESL Data layer components such as SQLJ Java Stored Procedures within Changeman SCM.
    • Assist TDM (Test Data Management) team in populating QA environments with obfuscated data; Db2 support for Content Manager (IBM Document Management System) and assist in regular software updates.
    Online since: Wed Nov 12 13:41:00 CET 2025
    Reference number: 847948/1

    Développeurs(euses) GraphTalk (m/f/d)

    Freelance/temporary employment for a project
    Valais
    • Develop and maintain insurance applications using Graphtalk AIA 3.0
    • Configure and parameterize new insurance products within the Graphtalk environment
    • Integrate interfaces such as Kafka, Java, and REST APIs
    • Collaborate with Data/AI teams to embed predictive models and decision engines
    • Support modernization and automation of business processes
    • Analyze and implement requirements from the social insurance domain
    • Document and ensure quality of developed solutions
    Online since: Wed Nov 12 13:36:52 CET 2025
    Reference number: 848825/1

    Global Clinical Program Manager (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Act as a planning expert in Clinical Operations Program Leadership, managing project information for decision-making across CDMA teams and leadership
    • Apply project management skills and clinical operations expertise to ensure timely, budget-compliant delivery of CDMA-related outcomes
    • Collaborate with other Clinical Program Managers, Portfolio & Project Management Office staff, and leadership to align deliverables
    • Drive patient- and customer-centricity by prioritizing patient needs and customer satisfaction in all activities
    • Partner across diverse regions and cultures to foster inclusion, belonging, and diversity within teams
    • Identify opportunities for collaboration across Clinical Development and Medical Affairs communities
    • Lead project management activities such as budget planning, tracking, reporting, risk management, and change management within clinical operations or diagnostic product development
    • Guide teams in resolving complex issues, influencing senior stakeholders to adopt new approaches and improve organizational outcomes
    Online since: Tue Nov 11 15:10:49 CET 2025
    Reference number: 848817/1

    Global Project Manager (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Set up and implement project, program, and product structures for development and product care activities
    • Create and maintain integrated project plans including dependencies, resources, and budgets
    • Ensure quality implementation in risk management, critical path analysis, scenario planning, and budget control
    • Guide teams through milestone reviews, capacity reviews, and continuous improvement initiatives
    • Apply project methodologies, including agile practices, and coach teams in hybrid agile/non-agile approaches
    • Manage meetings, knowledge sharing, and foster positive team dynamics
    • Establish and report KPIs, OKRs, and other metrics to measure project success
    • Identify risks, bottlenecks, and propose solutions to keep projects on track while communicating proactively with stakeholders
    Online since: Tue Nov 11 15:09:51 CET 2025
    Reference number: 848506/1

    Expert GLAS Data Maintenance Support (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • GLAS Data Maintenance (Maintain and update data in GLAS data systems)
    • GMP Training(Train the teams (like Procurement and Finance) who work with the GLAS on the new rules and how to keep the data clean)
    • GMP Documentation (Track how the cleanup is going and report the results to management regularly)
    • Ensuring data integrity (Put checks in place to prevent bad or incomplete information from entering the GLAS in the first place)
    Online since: Mon Nov 10 13:39:22 CET 2025
    Reference number: 847881/1

    Senior Associate in automated cell culture (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Operate and maintain automated cell culture systems for large-scale cell production
    • Support HTS campaigns and profiling assays by executing automated experiments
    • Plan experiments, order materials, and run biochemical and cellular assays on automated platforms
    • Analyze assay data and troubleshoot issues in workflows or automation systems
    • Collaborate with assay development teams across cellular, biochemical, biophysical, MS, and RNA domains
    • Contribute to the design of new cell culture systems with external vendors (optional)
    • Expand knowledge in lab automation and digital workflows
    • Work within a dynamic, inclusive matrix team focused on drug discovery
    Online since: Mon Nov 10 08:22:02 CET 2025

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