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    Reference number: 809837/1

    IMP Quality Manager clinical packaging (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Support all quality-relevant packaging processes and collaborate with packaging operations and all relevant interfaces with regard to GMP topics
    • Partner with stakeholders and provide GMP support to ensure successful delivery of the company goals
    • Review and release of manufacturing specifications and Batch Records (BR) of finished and semi-finished goods
    • Manage actively Deviations and Changes
    • Collaboration through to the management of local and global projectsActively engage in optimization activities and improvements within IMP Quality Clinical Packaging Switzerland. 
    • Coordinate improvement projects and engage in corrective and preventive measures (CAPA) 
    • Build, verify and implement standard documents (SOPs)
    • Joy in a human-centered and self-managed way of working based on NewWork, with a key focus to support the ongoing cultural and organizational change towards collaboration, agility and innovation mindset
    Online since: Tue May 20 16:02:28 CEST 2025
    Reference number: 822302/1

    Project Engineer Black Utilities (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Verification of ideas and requests, feasibility and conceptual studies for projects until the internal approval for execution together with the internal and external team members (Electrical-, Measurement- and Controls Engineering, Civil Engineering, HVAC-Engineering, 3D-Planning and Field Engineering/Construction Management, Fire protection, General Planners, and other Subject Matter Experts)
    • Plant Design and execution of projects, together with and coordinating of internal and external engineering partners until and including successful plant start-up
    • Support/accompaniment of 3D coordination, resolution of collisions, adjustments, etc.
    • Responsibility for commissioning and acceptance of the systems and participation in integral tests with general designer/architect, Lonza internal engineering disciplines, piping contractors, etc. incl. collection/control/handover of the as-built technical documentation to the end user and handover of the systems to the future owner and operator
    • Additional tasks as required by the Global Engineering Team
    Online since: Mon May 19 16:03:44 CEST 2025
    Reference number: 821515/1

    Technical Author (m/f/d)

    Freelance/temporary employment for a project
    Basel
    • Create and maintain technical documentation in the aviation sector
    • Aircraft Maintenance Supplements
    • Illustrated Parts Supplements
    • Cabin Crew Manuals
    • Passenger Safety Cards
    • Support and drive the transition from FrameMaker/Illustrator to a structured SGML/XML-based documentation system
    • Collaborate closely with internal teams and external tech doc providers
    • Option to take on deputy or full managerial responsibilities within the department
    Online since: Mon May 19 16:00:02 CEST 2025
    Reference number: 821958/1

    Global Study Manager (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Project/Study managers will be responsible for study supply leadership to ensure timely planning and execution of supply strategy for continued supply of clinical finished goods (supply drugs) to patients
    • Study managers provides inputs in clinical study protocol, understand study design and are responsible for optimal clinical trial supply strategy in terms of packaging design, pro- active planning following a risk-based approach
    • Represent Global Clinical Supply as a single point of contact (SPOC) at trial level for the integrated Clinical Trial team (iCTT)
    • Reviews overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule
    • Creates and maintains complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems
    • Creates and drives finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial
    • Defines clinical supply parameters for NIRT set up and initiates subsequent updates throughout the duration of the clinical trial
    • Develops and executes a trial-level project plan together with all other relevant roles
    • Identifies, assesses and proactively communicates supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
    • Collaborates with all relevant line function partners for country submission and approval timelines (including INDIMPD
    Online since: Mon May 19 10:28:06 CEST 2025
    Reference number: 821396/1

    Senior Process Validation Specialist (m/f/d)

    Freelance/temporary employment for a project
    Valais
    • Develop the strategy for the process-specific validations in biotechnology processes with focus on Mammalian Large Scale (ORCA) / Issue process validation/ study protocols and reports following VMP and SOPs (e.g. hold time studies, resin lifetime studies, buffer hold studies mixing studies, etc.) 
    • Participate in or moderate cross-functional Risk Assessments (RA) to define the scope of validation/ study activities / Assess validation data for conformance to protocol acceptance criteria and support the investigation and evaluation of deviations from the plans as well as the definition of associated corrective measures
    • Collaborate with QA in the definition of the standard for content, wording and scope of the validation documents and ensure that all validation documents comply with this standard
    • Issue, review or approve project related documents (RA, , TT documents, FMEA, etc.) and records (DR, CR, TCR)
    • Assessment of validation related technical change requests (TCR) and process-specific change requests (CR). Assessment of whether additional / new validation is required
    • Ensure the collaboration with QA Ops for batch release of process in validation, inclusive the approval of deviation reports and change request of validated processes
    • Coordinates preparation, processing, control and approval of CPV plans, CPV reports and PQRs as process validation specialist
    • Assist process development (PD) during process characterization studies and risk assessments
    • Act as a key member (i.e. technical lead) in cross-functional technical project teams and ensure the organization of meetings for an efficient collaboration with MSAT, QA Validation, Cleaning Validation and QA Qualification (as required)
    • Support (as requested) the establishment of a culture of continuous improvement throughout the organization
    Online since: Fri May 16 16:42:35 CEST 2025
    Reference number: 821813/1

    Project Manager Non IT (m/f/d)

    Freelance/temporary employment for a project
    Lucerne
    • Plan and manage project schedules (instrument/equipment qualification, software rollouts)
    • Provide routine status updates to stakeholders
    • Coordinate with US teams to standardize project templates and prioritization processes
    • Support budget tracking and purchase order preparation
    Online since: Thu May 15 16:19:05 CEST 2025
    Reference number: 821707/1

    Global Payer Value & Access Manager (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Refine global pricing, reimbursement, and access strategies that balance affordability, value, and sustainability across diverse markets
    • Define payer segmentation and engagement frameworks, considering procurement structures such as PAHO Revolving Fund, GAVI, UNICEF, national tendering systems, and private markets
    • Support with global pricing scenario analysis, accounting for factors such as competitor entry (e.g., pipeline vaccines, alternative technologies or shifting procurement trends), tendering strategies, and volume-based contracting
    • Support in refining life cycle pricing strategies, considering items such as multi-dose vial introduction, new evidence, policy shifts (e.g. new WHO recommendation) etc.
    • Monitor global market trends, competitor dynamics, and policy shifts that impact vaccine access (e.g., WHO guidance, HTA policy changes, and pandemic preparedness initiatives)
    • Support LOCs in defining, refining, and executing market access and pricing strategies, ensuring alignment with global guidance and best practices
    • Support NITAG engagements, including proactive and reactive responses, ensuring strong advocacy for vaccine inclusion in National Immunization Programs (NIPs)
    • Utilize AI-driven pricing analytics, real-world data (RWD), and forecasting models to optimize access strategies and anticipate shifts in procurement and reimbursement trends
    Online since: Thu May 15 15:24:45 CEST 2025
    Reference number: 821188/1

    Professional/Senior System-/Infrastructure Engineer (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • IT ownership of the business process area: Retail & Commerce B2C & Marketplaces. Owning the solutions (TechStack) and process area and driving it forward
    • Proactively collaborate with the business and product owners in analyzing, designing and planning requirements. Develop potential solutions for business needs or problem
    • Identify opportunities for customer-centric process improvements, while being responsible for the end-to-end process 
    • Define the value of improvements and adaptions of our solutions and measure the success of the implementation
    • Coordinate the external development suppliers in designing scalable and reliable technical solutions that will meet the business requirements in the best way
    • Coordinate and manage the quality, security and reliability (monitoring, testing, release management) of our solutions and the end-to-end business processes
    • Collaborate with colleagues to ensure smooth integrations of new digital solutions into the existing architecture
    Online since: Tue May 13 10:45:55 CEST 2025
    Reference number: 821190/1

    Profession/Senior Solution Architect Business Solutions (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • IT ownership of the business process area: Commercial B2B (Wholesale), including EDI. Owning the solutions (TechStack) and process area and driving it forward
    • Proactively collaborate with the business and product owners in analyzing, designing and planning requirements. Develop potential solutions for business needs or problem
    • Identify opportunities for customer-centric process improvements, while being responsible for the end-to-end process 
    • Define the value of improvements and adaptions of our solutions and measure the success of the implementation
    • Coordinate the external development suppliers in designing scalable and reliable technical solutions that will meet the business requirements in the best way
    • Coordinate and manage the quality, security and reliability (monitoring, testing, release management) of our solutions and the end-to-end business processes
    • Collaborate with colleagues to ensure smooth integrations of new digital solutions into the existing architecture
    Online since: Tue May 13 10:45:25 CEST 2025
    Reference number: 821192/1

    Professional/Senior Solution Architect Omnichannel Solutions (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • IT ownership of the business process area: Retail & Commerce B2C and Marketplaces
    • Owning the solutions (TechStack) and process area and driving it forward
    • Proactively collaborate with the business and product owners in analyzing, designing and planning requirements. Develop potential solutions for business needs or problem
    • Identify opportunities for customer-centric process improvements, while being responsible for the end-to-end process 
    • Define the value of improvements and adaptions of our solutions and measure the success of the implementation
    • Coordinate the external development suppliers in designing scalable and reliable technical solutions that will meet the business requirements in the best way
    • Coordinate and manage the quality, security and reliability (monitoring, testing, release management) of the solutions and the end-to-end business processes
    • Collaborate with colleagues to ensure smooth integrations of new digital solutions into the existing architecture
    Online since: Tue May 13 10:44:36 CEST 2025

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    Reference number: 821141/1

    Senior Research Associate (In vivo) in Non Malignant Hematology (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Work with transgenic mouse models to support different projects (injections, tissue collection and processing)
    • Run downstream ex vivo assays (e.g., multi color flow cytometry, qPCR, western blotting)
    • Work with cell lines, primary cells and tissues including patient-derived material
    • Collaboratively design, execute, and interpret data from different studies and contribute to assay optimization
    • Contribute to data analysis, maintain detailed documentation and effectively communicate findings to the research tea
    • Work closely with all members of the group, share duties, maintain a clean work environment and actively contribute to the positive work atmosphere within the group 
    Online since: Mon May 12 15:30:44 CEST 2025
    Reference number: 821075/1

    Senior Research Associate (In vitro) in Non Malignant Hematology (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Work with cell lines, primary cells and tissues including patient-derived material
    • Evaluate the efficacy and safety of novel therapeutic targets or compounds through genetic manipulation assays, ex vivo differentiation cultures, and various molecular assays (e.g., multi color flow cytometry, qPCR, western blotting)
    • Occasional work with transgenic mouse models to support different projects (tissue collection and processing)
    • Collaboratively design, execute, and interpret data from different studies and contribute to assay optimization
    • Contribute to data analysis, maintain detailed documentation, and effectively communicate findings to the research team
    • Work closely with all members of the group, share duties, maintain a clean work environment and actively contribute to the positive work atmosphere within the group
    Online since: Mon May 12 15:15:12 CEST 2025
    Reference number: 821149/1

    Senior Regulatory Affairs Specialist (m/f/d)

    Freelance/temporary employment for a project
    Luzern
    • Ensure timely preparation and submission of new local Marketing Authorization applications for assigned products as well as appropriate follow-up with the local authorities
    • Track process and manage answers to objections from the regulatory authorities on products registration and major new indications, involving negotiations to achieve best conditions
    • Participate in subsidiary product and launch teams to provide regulatory input and strategy advice
    • Ensure maintenance of assigned, authorized products through timely submission of variations, renewal applications and supplemental marketing authorizations
    • Ensure timely preparation and maintenance of local labels and packaging materials
    • Ensure high quality translations and check of labels
    • Ensure efficient and consistent implementation and use of internal and external regulatory databases and systems in Switzerland
    Online since: Mon May 12 15:06:15 CEST 2025
    Reference number: 820549/1

    Senior Manager Internal Engagement and Communications (m/f/d)

    Freelance/temporary employment for a project
    Bern
    • Through deep understanding of enterprise, business unit and site strategy and goals and partnering with other CEA and functional colleagues in the country, develop and own the country internal engagement strategy, and support of local external relations
    • Serve as the Swiss lead for Internal Engagement ensuring alignment with corporate messaging across all Swiss sites / Partner closely with HR, Operations, and Business Leaders to drive internal engagement initiatives that strengthen employee connection to the company’s mission and performance objectives
    • Provide regional perspective and insights for global enterprise communications / Develop and manage site communications for the Bern site ensuring that employees understand the company strategy and business unit objectives and fostering values-based culture
    • Participates in site leadership, assisting with planning, budgeting, and communications initiatives / Provides strategic counsel to Bern site leaders to ensure aligned messaging and increase internal and external engagement, community relations and media opportunities
    • Develops and executes strategic and leadership communications plans / Enhances company reputation and positioning in the community through local, site- specific media relations, community engagement, and digital communications
    • Customizes and implements site communications of global change initiatives to ensure they are timely, relevant and site-specific
    • Lead communications capability-building initiatives for site leaders to enhance their effectiveness as internal influencers and strengthen their ability to engage and motivate their teams
    • Acts as a primary communications lead for key site initiatives like office moves, consolidations and change initiatives
    • Develop and execute site-specific engagement activities, including town halls, leadership fire-side chats, and feedback mechanisms
    • Ensure site-level crisis communications are managed effectively in partnership with Corporate Affairs and the global reputation COE and the relevant business teams
    Online since: Fri May 09 12:07:42 CEST 2025
    Reference number: 820076/1

    CQV Leader Fill & Finish (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Filling and semi-stoppering (filling, dose control, closing (stoppering), sampling and rejection of vials) using Peristaltic and Piston pump dosing systems for Lyophilized vials.
    • Filling Isolator (Internal environment Grade A (Iso 5), HVAC system, H2O2 decontamination process and Glove integrity tester, Rapid transfer ports for transfer of materials). 
    • Lyophilizers with mass spectrometer and dedicated loading and unloading isolator each. 
    • ATEC Stopper treatment station and loading arm into the isolator
    • Ensure that CQV activities are executed in accordance with the C&Q Plan and supporting Validation Plans.
    • Overall planning and execution of the commissioning activities related to allocated areas or systems.
    • Leading and coordinating the C&Q execution effort supported by C&Q EPC teams, Engineering, Operations, and external vendors and contractors
    • Planning and scheduling the commissioning activities according to the C&Q strategy and supporting Validation Plans. 
    • Support the updates of Master C&Q Plan and supporting plans during project execution lifecycle. 
    • Support development of C&Q schedule by including the activities relevant for the preparation of commissioning test plans and test specifications
    • Coordinating the planning and scheduling of commissioning activities with the construction interface and with other disciplines (HSE, Automation, Electrical, Instrumentation, Operation and Engineering, etc.)
    Online since: Mon May 05 14:52:43 CEST 2025
    Reference number: 819896/1

    DevOps Engineer (m/f/d)

    Freelance/temporary employment for a project
    Fribourg
    • Designing, developing and operating effective and innovative functionalities for a customer- and agent- facing B2B billing system
    • Developing and refactoring complex parts for the backend of the system with Java, Spring Boot and OPA
    • Implementing user-friendly frontend elements with React
    • Refining and optimizing database queries to enhance the overall system performance
    • Conducting code reviews, ensuring that the team's output is of high quality and aligned with our overall technical objectives
    • Performing deployment and releasing activities as well as monitoring and managing system errors
    • Taking responsibility for high system availability also outside office hours as part of the on-call service
    Online since: Fri May 02 16:01:14 CEST 2025
    Reference number: 819578/1

    Country Manager Switzerland (m/f/d)

    Permanent employment with our customer
    Zürich
    • Establishing and leading the Swiss branch
    • Developing and managing strategic and operational business in the Swiss market 
    • Identifying new business opportunities
    • Developing and implementing sales strategies
    • Close cooperation with the Italian based parent company
    • Building and maintaining relationships with clients and partners
    • Preparing reports and tracking the company's performance in Switzerland
    Online since: Fri May 02 11:58:08 CEST 2025
    Reference number: 819812/1

    Electronics IVVQ Engineer (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Defining test setups for electrical applications, using both commercial test equipment and/or custom-designed test equipment
    • Assist for the definition, design, build and testing of custom test equipment and test electrical harnesses (Ground Support Equipment “GSE”) needed to operate the test item
    • Writing Test Plans, AIT Plans, test procedures and test reports to ECSS quality standards
    • Testing of the performance of the electronics test item (equipment) and of the system to achieve defined requirements (at both board level, equipment level and system level)
    • Handling of requirements verification by test
    • Implement automated testing using Python-based software to interface with custom-designed and commercial test equipment and the Device Under Test (DUT)
    • Definition and performing thermal tests (thermal vacuum and/or nitrogen gas environment thermal tests); mechanical testing (vibration and mechanical shock testing) for the electronics equipment item
    • Electromagnetic compatibility (EMC) testing to ECSS standards
    Online since: Wed Apr 30 14:43:51 CEST 2025
    Reference number: 819692/1

    Commercial Operations Director (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Support the commercialization of Qdenga in travel markets
    • Manage EUCAN sales report development with the input from LOCs and the support of a vendor. Initiate periodic format revisions and update accordingly
    • Develop and / or migrate data repositories with the purpose of creating a history bank for all key events including housing of meeting materials (VRLT; Community Forum) and presentations such as business reviews, LOC brand plans; listing and tracking of clinical recommendations etc.
    • Support EUCAN travel LOC engagements by scheduling, planning, coordinating and minuting meetings
    • Support key growth initiatives in line with the needs and requirements of travel LOCs
    • Support the logistics of coordinating activities related to key regional congresses in collaboration with the host EUCAN LOC
    • Liaise closely with VBU and EUCAN functional counterparts to support travel market needs, including medical, access, and marketing
    • Lead the EUCAN CSEE and the Wave 3 Launch LOC needs and oversee LOCs in identifying marketing and stock needs and support or channel requests to the appropriate persons
    Online since: Wed Apr 30 10:35:02 CEST 2025
    Reference number: 817609/1

    Engine Architect - Combustion Engine (m/f/d)

    Freelance/temporary employment for a project
    Fribourg
    • You define the architecture of new engine projects and monitor engine trends
    • You can solve the most complex technical issues by coordinating design, simulation, and testing
    • You design and optimize high-complexity components
    • You perform the 3D drafting of components and assemblies using CAD systems, and create and revise 2D drawings with GD&T
    • You generate 2D and 3D visualizations for clarifying technical content, including setting up technical presentations
    • You ensure reporting to top management on specific technical topics
    • You cooperate with component suppliers to clarify technical properties and engage in common component development (co-design)
    • You actively contribute to FMEA (Failure Modes and Effects Analysis
    • You coordinate other design resources while ensuring the quality of deliverables and collaborate with various departments within the project environment
    Online since: Tue Apr 29 15:54:34 CEST 2025
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