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Jobs by e-mail

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    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: 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
    Reference number: 831001/1

    Bioprocess Engineer DSP (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Oversees, plans and supports execution of manufacturing campaigns in the area of microbial fermentation
    • Responsible to prepare and execute SHE, EM, operation and cleaning risk analysis for the assigned products and the implementation and control of defined measures
    • Responsible to establish timely and with high quality the required production documentation (preparation and review of electronic batch records) specific to the assigned production area
    • Perform manufacturing activities according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution
    • Reviews production documentation and works on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards
    • Working as production expert in Capital investment projects for building and commissioning of the manufacturing units
    • Responsible for delivering all input required for the specific set-up, commissioning and qualification of the manufacturing suites and equipment including automation
    • Prepares changes and reviews DeltaV recipes for equipment and facility parts
    • Coordinates and supports Engineering and workshops for campaign preparation and change-over activities in the facility
    • Responsible for training of the operators for the manufacturing of the assigned products
    Online since: Mon Jul 28 16:16:17 CEST 2025
    Reference number: 804403/1

    Clinical Development Lead Oncology (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Serve as a subject matter expert for Liver Oncology, clinical study design and evidence generation strategies for internal and external stakeholders in the assigned indication area.
    • Responsible for critical review of study results, protocol and report generation to support new product development.
    • Works with colleagues from Business, Medical Affairs, Clinical Operations, Regulatory Affairs, Biometrics, Development, Quality, and other functions to ensure appropriate implementation of clinical development strategies.
    • Builds and maintains strong, collaborative relationships with cross-functional leaders, key internal and external stakeholders and other alliance partners, in meeting business goals and ensuring operational excellence.
    • Act as an ambassador and representative of Clinical Development establishing effective collaborative relationships with key functions for new and existing products, incl. clinical utility, intended use and claim extensions.
    • Play a leadership role in maintaining clinical, regulatory, and scientific expertise as it relates to IVD product development and regulatory documentation. Leads medical/scientific input and preparation of regulatory submissions as well as responses to reviewers from regulatory agencies.
    • Drives competitive differentiation, innovation and early pipeline activities and develops intellectual property strategy.
    • Responsible for comprehensive literature reviews, supervises collation of relevant clinical and scientific information from different sources, and creates new scientific content (without guidance/direction).
    • Demonstrate leadership skills; ability to mentor and provide an environment for personal and professional growth.
    Online since: Wed Jul 23 10:45:58 CEST 2025
    Reference number: 830982/1

    Trail Master File Specialist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Strategic management of the document lifecycle in eTMF: creation, versioning, review, approval and archiving - always in line with regulatory requirements and study timelines
    • Quality control (QC) and review of study documents to ensure GCP compliance
    • Participation in the development and optimization of SOPs, work instructions and forms in the eTMF environment
    • Regular review of the completeness and quality of the TMF in accordance with the TMF plan
    • Support with audits and inspections
    • Coordination of digitization and integration of paper-based and external TMFs
    • Administrative tasks in the eTMF system, e.g. user administration and maintenance of global directories
    Online since: Thu Jul 17 16:07:00 CEST 2025
    Reference number: 830730/1

    Clinical Research Associate (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures, good clinical practices and other applicable regulatory requirements
    • Validating product performance claims
    • Supplying data for critical Regulatory submissions
    • Defining the functional and clinical utility of investigational products
    • Obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders
    • Interfacing with cross functional staff to support post launch activities
    • Reviewing cases with investigators to resolve discrepancies
    • Ensuring that studies adhere to FDA regulations, Good Clinical Practices, IVD directives, and Roche policies and procedures
    Online since: Thu Jul 17 14:37:50 CEST 2025
    Reference number: 830174/1

    Clinical Quality Assurance Specialist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Support in clinical GCP QA activities
    • Development of protocols and review of studies
    • Evaluation from the QA perspective
    • Creation and review of SOPs in the clinical team
    • Pragmatic thinking and innovative problem solving
    • Remote and on-site work as required
    Online since: Mon Jul 14 10:35:45 CEST 2025

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    Reference number: 829983/1

    CMMS SME Specialist (m/f/d)

    Freelance/temporary employment for a project
    Neuchatel
    • Management of CMMS datas
    • Equipment / Measure instrument / TAGs creation
    • Spare-parts creation and codification
    • Creation / Modification / delation of Equipment Part-list
    • Creation / Modification / delation of preventive and predictive maintenance Work-order
    • Creation / Modification / delation of preventive calibration Work-order
    • Hierarchy management of equipment in the systems
    • Parameters modification and management of the documentation and formation support linked to the CMMS systems
    • Dispense formation to all employees who need to have access to the CMMS System 
    • Participation on CAPEX project as needed
    • Management of all project linked to the CMMS system
    Online since: Fri Jul 11 14:08:05 CEST 2025
    Reference number: 829942/1

    Automation Leader (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Provide design support for the generation and configuration of the DeltaV system configuration for the following utility and process systems which are monitored and controlled by the DeltaV DCS
    • Black and Clean Utility generation, storage and distribution systems; Heating Ventilation and Air Conditioning for the classified and non-classified areas within the site manufacturing and utility areas; Environmental Monitoring System;Compounding and SIP/CIP system
    • Review and approve Automation Requirements, Design, Test, Qualification and Validation documentation
    • Provide guidance and technical direction to the external System Integrator for the generation and testing of the DeltaV DCS software configuration
    • Support software FATs and SATs by approving documents and witnessing on behalf of Lonza as the Lonza Automation Representative
    • Support the integrated commissioning of the DeltaV system software, hardware and interfaces to the various process and utility systems listed above
    • Support the 3rd Party Package Unit (PU) integration into the overall Project Dolphin Automation / OT landscape, including mapping the data interface and data exchanges between DeltaV and the PUs
    • Support the reliable operation of the various control systems by providing hands on support to trouble shoot control system software and hardware issues
    • Support the overall Dolphin Project Team to collate supporting information to allow timely decisions to be made that will minimize cost, timeline and quality impact on the Project
    • Collaborate with the MES team to facilitate deployment of electronic log books eLogs, and integration with DeltaV
    Online since: Thu Jul 10 12:09:40 CEST 2025
    Reference number: 829916/1

    Research Associate Mass Spectrometry (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • In this lab based role, you will implement, optimize and use LC-MS workflows for metabolites, lipids and proteins, including sample preparation, measurement, data analysis and reporting
    • You will prepare and analyze samples from cell culture and tissue using mass spectrometry
    • You present and discuss your data and findings with colleagues
    • You work collaboratively with your colleagues to contribute to general laboratory operations within the MS team, including instrument maintenance, and troubleshooting
    Online since: Thu Jul 10 12:04:16 CEST 2025
    Reference number: 829639/1

    Supply Chain Planning System Adoption Lead (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Develop and deliver comprehensive training programs for system users
    • Conduct change assessments and surveys to gauge system adoption readiness
    • Create and maintain detailed documentation including process flows, training guides, and user manuals
    • Impact Analysis: Assess how changes to the planning system will affect various business units, processes, and roles. Create mitigation strategies for potential resistance
    • Identify areas for continuous improvement and recommend adjustments to enhance efficiency and user experience
    • Behavioral Reinforcement Plans: Design initiatives to reinforce desired behaviors post-implementation, including coaching, mentoring, and feedback loops
    Online since: Wed Jul 09 15:50:37 CEST 2025
    Reference number: 825238/1

    Medical Director (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Overseeing of medical monitoring of clinical trials is a must (robust experience)
    • Medical Data Reviewing to ensure data quality and integrity in ongoing studies (robust experience)
    • Management and medical-scientific responsibility for clinical development programs, especially in phases II and III
    • Close collaboration with clinical operations, regulatory affairs, safety and other internal stakeholders
    • Supporting the creation and review of medical content for study related documents, e.g. protocols, medical monitoring plans, clinical study reports
    Online since: Tue Jul 08 15:51:54 CEST 2025
    Reference number: 829417/1

    Scientist Lab Technician Assay Development (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Working with high throughput lab – analyzer
    • Routine lab work with infectious samples and leading of own experiments including the analysis of them
    • Plan and execute different work packages for the development of molecular diagnostics test
    • Participation in project meetings and presentation of experimental data
    • Precise documentation of experiments using electronic lab journals according to GMP Standards
    • Equipment handling and maintenance
    • Statistical data analysis using different software and tools (e.g. JMP)
    • Author official documents (e.g. Design History Files)
    Online since: Tue Jul 08 15:51:26 CEST 2025
    Reference number: 829428/1

    Expert Chemicals Management & Lab Workflow Lead (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Ordering chemicals & drugs for PCR AD
    • Chemical inventory management / Chemical safety responsible / Chemical room responsible / Chemical waste management: empty bins, expired materials / Chemical training responsible (e.g. chemical spill trainings)
    • Maintain a chemical storage concept (Lagerkonzept) in AD
    • Collaborate with stakeholders to shape, test, and continuously improve new digital chemical inventory solutions, ensuring seamless integration with lab workflows and adherence to safety standards
    • Collaboration with stakeholders within the department (e.g. Development Project Teams) and outside of the department (e.g. Site SHE, RnD Services, Site Services, Site Logistics, Procurement, Service technicians, Medicals, etc...)
    • Responsible for a small chemical support team (2-3 people) and involved in hiring activities of new team members, onboarding activities and development of chemical team members, in collaboration with the AD People Leaders
    • Audit support
    • Proactively Identify areas for lab workflow improvements in the biosafety level 2 laboratories of Assay Development and drive the implementation in the function as Lab Workflow Lead in collaboration with department internal and external stakeholders
    Online since: Tue Jul 08 15:45:22 CEST 2025
    Reference number: 829507/1

    Global Project Manager (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Sets up and manages structures for product development and care, covering timelines, budgets, resources, and communication
    • Creates and maintains integrated project plans to support efficient teamwork and delivery
    • Leads milestone and capacity reviews, drives process consistency, and shares best practices
    • Applies project methodologies, including Agile and hybrid approaches, and supports teams in using them effectively
    • Facilitates meetings, encourages knowledge sharing, and builds strong team dynamics
    • Defines and tracks KPIs, OKRs, and other metrics to improve project quality and efficiency
    • Advises teams and leadership with planning, risk management, and scenario analysis to support decision-making
    • Identifies risks, gaps, and delays, proposes solutions, and communicates proactively with stakeholders
    • Manages project data to support teams and leadership with planning and portfolio decisions
    • Collaborates with cross-functional partners to ensure smooth delivery and coaches peers for growth
    • Identifies improvement opportunities and suggests solutions within the project management function
    Online since: Tue Jul 08 15:03:08 CEST 2025
    Reference number: 813894/1

    Design Engineer - Environmental Safety (m/f/d)

    Freelance/temporary employment for a project
    Visp
    • Lead the implementation of EHS standards and practices throughout the project lifecycle
    • Collaborate with design teams to ensure safety, environmental, and sustainability aspects are embedded into project designs
    • Participate to risk assessments, including HAZOP, ATEX, containment, and fire safety evaluations during the different project phase (from feasibility to detail design)
    • Maintain accurate records of basic container data to facilitate on-demand reporting and dashboard creation, including regular inspections to verify current conditions
    • Ensure compliance with local, national, and international EHS regulations and standards (e.g., SUVA)
    • Ensure preparation of documentation for apply for necessary approvals for project execution
    • Maintain documentation to support regulatory audits and compliance checks
    • Act as the primary EHS representative for projects, working closely with engineering teams
    • Develop and manage EHS deliverables, including initial assessments, CAR reviews, and operational safety plans
    • Monitor project progress against defined EHS milestones, providing updates to stakeholders
    Online since: Wed Jul 02 16:20:28 CEST 2025
    Reference number: 828731/1

    Senior Scientist Tech transfer (m/f/d)

    Freelance/temporary employment for a project
    Neuchatel
    • Responsible for supporting commercial manufacturing performance at the external manufacturing site
    • Represent MS&T external manufacturing team to provide technical support to the biological drug substance tech transfer process including deviation resolution, change management, delivery of yield targets and process optimization
    • Maintain strong working relationships with external and internal partner
    • Interface with internal functions such as MS&T, Quality, and Supply Chain
    • Develop and maintain strong technical familiarity with process and process equipment, process optimization evolution and technical problem solving
    • Tracks progress of routine manufacturing against schedule, provides routine updates and proactively identifies operational risks and remediation
    • Ensure timely escalation of potential technical, compliance or safety issues to the MS&T team and partners with internal MS&T resources to remediate
    • Ensure effective communication between technical transfer internal and external team
    • Support technology transfer activities as a primary duties
    • Implement and maintain high standard of quality and regulatory compliance to meet and exceed regulatory agency and quality requirements
    Online since: Wed Jul 02 16:12:02 CEST 2025
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