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    Reference number: 835199/1

    CAPEX Program / Project Manager (m/f/d)

    Freelance/temporary employment for a project
    Bern
    • Set up a program of projects that all aim to resolve safety gaps
    • Responsible for project activities required to scope, develop, procure, construct and qualify new equipment and facilities required to meet facility production throughput demands 
    • Leads multi-disciplinary Teams through project life cycle activities to deliver capacity expansion capabilities to meet global and local strategic requirements 
    • Develops and maintains integrated project plans and monitors project activities for adherence to milestone timelines, deliverables and budget against approved plan
    • Maintain oversight on project risks and develops risk mitigation strategies
    • Ensures that initiatives are aligned with the business objectives and strategic philosophy 
    • Responsible for providing cGMP compliant processes and facilities suitable for FDA and global regulatory approval 
    • Responsible for implementing EHS by design principles in the project
    • Responsible for generation of regular project reports (financial updates, project schedules, risks and summary of current activities) for site Sr. Management and Global Steering Committees
    • Project Teams are responsible for completion of project lifecycle activities through performance qualification
    • Influences teams to work collaboratively, to be customer focused and to deliver superior performance through personal leadership abilities, mentoring and effective communication
    Online since: Tue Aug 12 16:20:07 CEST 2025
    Reference number: 834990/1

    Biotechnologist (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Execute manufacturing activities for liquid and freeze-dried drug products in compliance with cGMP guidelines
    • Ensure safe, timely, and quality-compliant batch execution, including troubleshooting and resolving equipment issues
    • Provide frontline technical and procedural support to the manufacturing team
    • Prepare, execute, and review batch records and other GMP documentation with high accuracy and timeliness
    • Support investigations and decision-making processes related to production issues
    • Contribute to process changes and CAPA implementation within defined timelines
    • Operate, set up, and clean production equipment and premises (e.g., compounding, parts washing, autoclaving, filter integrity testing, visual inspection)
    • Conduct training activities for operators and support onboarding of new team members
    Online since: Mon Aug 11 13:45:25 CEST 2025
    Reference number: 834994/1

    Bioprocess Engineer DSP (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Plan and oversee manufacturing campaigns in downstream processing
    • Prepare and execute risk analyses (SHE, EM, operational, cleaning) for assigned products
    • Create and review electronic batch records and production documentation
    • Perform manufacturing activities in compliance with cGMP guidelines
    • Troubleshoot equipment issues and recommend solutions
    • Review documentation and manage deviations, change requests, and CAPAs
    • Act as production expert in capital investment projects (setup, commissioning, qualification)
    • Prepare and modify MES and DeltaV recipes for equipment and facilities
    • Coordinate engineering and workshop activities for campaign preparation and changeovers
    • Represent the production unit during customer audits and site visits
    Online since: Mon Aug 11 13:44:04 CEST 2025
    Reference number: 834967/1

    Process Engineer Black Utilities (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Develop and verify project ideas and requests, including feasibility and conceptual studies
    • Collaborate with internal and external partners across disciplines (e.g., electrical, civil, HVAC, fire protection, 3D planning)
    • Ensure regulatory requirements and internal guidelines are considered during project development
    • Coordinate plant design and execution through to successful start-up
    • Support 3D coordination, resolve design collisions, and implement necessary adjustments
    • Oversee commissioning and acceptance of systems
    • Participate in integral testing and ensure proper documentation handover to end users
    • Transfer ownership of systems to future operators
    • Prepare technical documentation and specifications in collaboration with project teams
    • Take on additional tasks as required by the Global Engineering Team
    Online since: Mon Aug 11 13:29:04 CEST 2025
    Reference number: 834960/1

    CQ Engineer HVAC (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Develop and approve system boundaries for HVAC systems
    • Prepare, execute, and approve Design Qualification (DQ) documents
    • Conduct GMP Risk Assessments (GMP-RAs) for relevant systems
    • Prepare, execute, and approve commissioning activities, including vendor supervision
    • Prepare, execute, and approve Installation Qualification (IQ) documents
    • Prepare, execute, and approve Operational Qualification (OQ) documents
    • Support execution of Design Qualification for other direct impact systems
    • Assist in implementing the installation and commissioning process per project guidelines
    • Provide cross-functional support in other commissioning and qualification activities as needed
    • Apply interface management and proactively solve problems during execution
    Online since: Mon Aug 11 13:12:12 CEST 2025
    Reference number: 834963/1

    CQ Engineer Clean Utilities (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Develop and approve system boundaries for clean utility systems
    • Prepare, execute, and approve Design Qualification documents, including release for Installation Qualification
    • Conduct GMP Risk Assessments (GMP-RAs)
    • Prepare, execute, and approve commissioning activities, including vendor supervision and quality control
    • Prepare, execute, and approve Installation Qualification documents, including release for Operational Qualification
    • Prepare, execute, and approve Operational Qualification documents, including release to operations
    • Support Design Qualification execution for other direct impact systems
    • Assist in implementing installation and commissioning processes per project guidelines
    • Collaborate across CQV activities and support other tasks when needed
    • Apply interface management and proactively solve problems; shift work may be required
    Online since: Mon Aug 11 13:04:25 CEST 2025
    Reference number: 834546/1

    Technical Package Lead (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Act as BioAtrium’s primary contact for operational integration of assigned engineering scope items
    • Coordinate between EPCM partner, contractors, and internal teams to ensure GMP-compliant execution
    • Create, update, and structure project documentation (URS, TS, FDS, HAZOP, IQ/OQ/PQ protocols)
    • Ensure documentation aligns with internal quality and document control standards
    • Draft and review Change Requests (CRs) and Technical Change Requests (TCRs)
    • Ensure technical accuracy and GMP compliance in all change-related documentation
    • Provide technical oversight for mechanical adaptations and scope-specific activities
    • Support EPCM partner in supervising contractors during integration
    • Collaborate cross-functionally with Manufacturing, QA, Engineering, Validation, and EPCM teams
    • Track progress of scope items against project milestones and propose mitigation strategies for delays
    Online since: Thu Aug 07 15:14:07 CEST 2025
    Reference number: 827282/1

    System Engineer (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Development of models using Matlab and Simulink
    • Analysis of product defects and visualization of errors on displays
    • Performing tasks based on model-based-system engineering
    • Testing and validation of developed models and software in workshop/laboratory environments
    • Conducting simulations and tests directly on the device (e.g., engines or specific components)
    • Close collaboration with other departments
    Online since: Thu Aug 07 15:10:33 CEST 2025
    Reference number: 834632/1

    Software Engineer (C++, Squish, Python) (m/f/d)

    Freelance/temporary employment for a project
    Geneva
    • You create and maintain the Software Requirements Specification and also the test cases
    • You review and test against the Software Requirements Specification and establish test traceability
    • You write automatic test scripts for test automation environment (C++, Squish, Python)
    • You execute manual and automatic tests and report results
    • You analyze and describe issues/bugs in our issues Database JIRA
    • You synchronize and update the Test Results Management tool
    • You perform formal system tests (Factory Acceptance Test)
    • You perform analysis of defects/incidents to find the root cause of problem
    • You may contribute to development activities
    Online since: Thu Aug 07 14:43:09 CEST 2025
    Reference number: 834508/1

    Regulatory Affairs Manager (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Contribute to defining and executing EUCAN or GEM regulatory strategies to support product development and patient access
    • Lead or support submission working groups and manage investigational and life-cycle applications in collaboration with global, regional, and local teams
    • Prepare for and participate in meetings with Health Authorities, represent Takeda when needed, and manage follow-up actions
    • Stay current with regional regulations and guidance, assess impact on development plans, and contribute to internal policy updates
    • Track and fulfill post-marketing commitments, ensuring ongoing regulatory compliance throughout the product life cycle
    • Effectively present regulatory strategies, timelines, and risk assessments to leadership and cross-functional teams
    • Build strong relationships with LOC Regulatory Leads, global teams, consultants, and business partners to align on access and submission goals
    • Support innovative patient access strategies and partner with access functions to ensure regulatory documents meet value and access needs
    Online since: Thu Aug 07 09:56:27 CEST 2025

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    Reference number: 834383/1

    ASPIRE Sustainment Supporter (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Align input across DIA BPM functions (Customer Service, Supply Chain, Regulatory & Quality, etc.)
    • Represent consolidated viewpoints in program discussions
    • Facilitate preparation for meetings and decision-making
    • Proactively identify and moderate potential conflicts or misalignments
    • Drive clear, consensus-based outcomes
    • Stakeholder management
    • Foster Cross-functional collaboration
    • Conflict resolution
    Online since: Wed Aug 06 13:51:45 CEST 2025
    Reference number: 834265/1

    Digital Biomarker Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Develop scientific core messages for product marketing
    • Support interactions with customers during the pre- and post-sales phases
    • Contribute to the communication of scientific results at conferences, in white-papers, and in peer-reviewed publications
    • Provide scientific guidance for data analysis projects
    Online since: Wed Aug 06 11:32:03 CEST 2025
    Reference number: 834007/1

    Project Technical Leader (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Develop URS and TechSpecs for AVI in IV bag applications
    • Conduct full-scale technology scouting, including vendor landscape analysis (qualified, early adopters, PoC, roadmap)
    • Request and analyze budgetary quotations; perform vendor evaluations using KT-analysis
    • Lead feasibility studies with vendors and document outcomes
    • Design process layouts and develop holistic Concept Designs
    • Facilitate supplier feedback and refine technical and commercial proposals
    • Recommend preferred supplier and ensure handover to Basic Design
    • Ensure execution readiness and alignment with project timelines 
    Online since: Tue Aug 05 14:26:46 CEST 2025
    Reference number: 833603/1

    Technical Lead Embedded Software (m/f/d)

    Freelance/temporary employment for a project
    Hinwil
    • Technical Lead in software development team for a RTOS based platform
    • Guide Embedded SW domain resources in terms of quality, estimations, work results
    • Run SW waterfall-type sub-projects (estimation, planning, requirements elicitation, resourcing, risk management)
    • Create high quality UML designs and write corresponding C++ code
    Online since: Fri Aug 01 13:23:11 CEST 2025
    Reference number: 833589/1

    Laboratory Technician QC (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Perform analytical testing of final and intermediate products, in-process samples, cleaning validation samples, utilities and environmental monitoring samples
    • Support method transfer, development, and validation, including equipment qualification for analytical use
    • Participate in maintenance, calibration, and proper use of laboratory equipment
    • Assist in training and qualification of new laboratory employees
    • Create and revise SOPs, Work Instructions, and other quality-related documentation
    • Ensure timely ordering and inventory management of laboratory materials and consumables
    • Document all laboratory activities, deviations, and errors in compliance with GDP standards
    • Collaborate in resolving chemical and biochemical issues, including quality concerns and regulatory inquiries
    • Communicate effectively with the QC Manager and team regarding ongoing activities, deviations and project updates
    • Adhere to GMP, EHSS, and company values, actively contributing to safety and quality improvement initiatives
    Online since: Fri Aug 01 11:58:34 CEST 2025
    Reference number: 833092/1

    Supplier Quality Engineer (m/f/d)

    Freelance/temporary employment for a project
    Hinwil
    • Support and monitor the supplier APQP process for new development and changes
    • Support D-FMEA and P-FMEA and its documentation and actions
    • Support evaluation and validation of testing equipments (e.g. MSA's) for production at Supplier
    • Plan and execute process/production release at suppliers for components/sub-assemblies
    • Perform PPAP for zero series and changes
    • Review safe launch concept at supplier during ramp-up phase and lead component suppliers to confirm serial capabilities
    Online since: Wed Jul 30 17:06:37 CEST 2025
    Reference number: 833258/1

    Plant Engineer (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Manage and execute small-scale modification and improvement projects
    • Ensure cGMP compliance of assigned systems throughout their lifecycle
    • Act as SME for single-use and disposable technologies and provide training to team members
    • Serve as the primary contact during audits and inspections for assigned systems
    • Support investment projects across all phases as engineering SME and final customer
    • Lead qualification and requalification activities for assigned equipment
    • Develop and implement asset management and maintenance strategies
    • Coordinate technicians and ensure compliance with internal and external standards
    • Provide second-level on-call support for production troubleshooting
    • Collaborate with cross-functional teams to support system lifecycle activities
    Online since: Wed Jul 30 16:16:21 CEST 2025
    Reference number: 833313/1

    Analytical Scientist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Developing a phase-appropriate control strategy for pharmaceutical dosage forms, encompassing the active ingredient and its precursors
    • Collaborating effectively with stakeholders across various departments, including drug substance and drug product process development and manufacturing, Technical Regulatory Affairs, Quality Assurance, and both internal and external analytical partners (such as service providers and commercial manufacturing/testing/packaging sites)
    • Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls, generating packaging-specific stability data, and ensuring thorough documentation
    • Coaching technicians on project work and serving as a central point of contact for project-related information
    Online since: Wed Jul 30 15:59:46 CEST 2025
    Reference number: 832999/1

    Senior Scientist Monitoring (m/f/d)

    Freelance/temporary employment for a project
    Lengnau, Berne
    • Setting up and maintaining systems for monitoring clean media and environmental conditions
    • Contact person for projects in the field of monitoring
    • Creating and maintaining SOPs, work instructions, and templates for qualification and monitoring
    • Performing risk analyses to define sampling points
    • Support in the creation of qualification protocols and reports
    • Development and implementation of monitoring and trending programs
    • Cooperation with internal interfaces for the efficient implementation of monitoring activities
    • Support in the introduction of LIMS and other IT tools
    • Participation in the processing of deviations in the monitoring area
    • Presentation of strategies and documents during audits and inspections
    Online since: Wed Jul 30 15:55:27 CEST 2025
    Reference number: 833271/1

    Medical Information Manager (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Ensure appropriate, quality and timely responses to requests for medical information in EMEA for therapeutic areas of responsibility 
    • Develop or adapt available medical information content to be used globally 
    • Support novel channels for dissemination of medical information 
    • Support new digital technologies and systems in accordance with GMI digital strategy 
    • Manage medical information providers •Develop and implement medical information support materials in coordination with Global Medical Teams and Medical Communications, as well as Local Medical Information teams, where appropriate 
    • Ensure reporting of potential adverse events and product quality complains to appropriate teams
    Online since: Wed Jul 30 15:35:55 CEST 2025

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