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112 Ergebnisse

112 Ergebnisse

    Referenznummer: 785379/1

    Automation Engineer (m/f/d)

    Permanent employment with our customer
    Aargau
    • Participate in automation projects within a team consisting of Automation Engineers, CQV engineers, and CSV engineers, contributing as an essential member of the DeltaV team
    • Write code in a DeltaV System
    • Code testing
    • Commissioning
    • Apply Good Manufacturing Procedures (cGMP) principles
    • Support the definition, execution and documentation of qualification tests
    Online seit: 27.09.24
    Referenznummer: 783868/1

    Kubernetes Atlassian SecDevOps Engineer (m/f/d)

    Freelance/temporary employment for a project
    Visp, Valais, Switzerland
    • Responsible for designing and maintaing containerized solutions
    • Design and implement cloud or on-premise infrastructure for IT and OT together with the IT and OT infrastructure representatives which need to meet the highest levels of GxP requirements, IT security controls and reliability.Define cloud standards and frameworks in order to manage the entire infrastructure lifecycle with DevOps techniques and technologies like: Hardware provisioning (Infrastructure as code), CI/CD pipelines, Testing automation framework, Artifact repositories (Releases, images...), Logs management and aggregation, Events/Metrics management and aggregation, Alert system, Apps building and deployment and Authentication and security framework
    • Responsible for proper Design according to IT Security and QA standards and procedures conducting reviews against architecture standardsEnsure that forward looking architectures, including new applications, move to cloud native setups. In order to provide a single pane of glass for IT and OT management, strengthen business resilience, etc.
    • Ensure that forward looking architectures, including new applications, move to cloud native setups. In order to provide a single pane of glass for IT and OT management, strengthen business resilience, etc.
    • Define, drive and implement new working methodologies using modern agile approach in collaboration with relevant stakeholders.
    • Look for improvements and enhancements to infrastructure systems that will ultimately provide more efficient services to the business
    Online seit: 20.09.24
    Referenznummer: 783908/1

    RFQ LDC Adopt enablement Readiness manager (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Go-live Readiness Assessments: Design a strategy covering data migration, testing, training, and communications for smooth execution. Ensure a seamless transition by consolidating all moving parts and resolving gaps.
    • Cutover Strategy: Collaborate with the Cutover team and create a blueprint for system transition, ensuring minimal disruption and business continuity, including definition of Milestones & KPIs tracking for clear progress and transparency.
    • Cutover Execution: Responsible for the governance of cutover activities like system freezes, migration, validations, and final go-live, working together with the Cutover team, while maintaining global alignment.
    • Risk Mitigation: Identify risks and implement mitigation strategies to avoid delays.
    • Documentation: Ensure comprehensive cutover and hypercare documentation for future use
    • Hypercare Management: Responsible for the governance of post-go-live support, working together with the Hypercare team, resolving issues and stabilizing the system.
    • Business-IT Alignment: Ensure critical processes function smoothly post-cutover with IT and business coordination.
    • Stakeholder Communication: Keep stakeholders informed of Cutover/Hypercare progress, risks, and updates.
    • Resource Training: Manage resources and ensure teams are trained for cutover roles.
    • Automation Integration: Promote the use of tools and automation to streamline cutover activities.
    Online seit: 19.09.24
    Referenznummer: 777421/1

    Knowledge Engineer (m/f/d)

    Freelance/temporary employment for a project
    Basel region
    • Collaborate with various product teams to shape the development and integration of data models and standardization into the RIS product portfolio and enable FAIR (findable, accessible, interoperable, reusable) data services
    • Collaborate with engineering and business teams and co-drive projects to implement interoperability standards for Roche devices and digital products adhering to FAIR principles
    • Investigate innovative methods to generate new business insights from interlinked data sources (lab and clinical) that may mature into new features of RIS digital products
    • Drive the adoption and integration of interoperability standards including terminological resources (e.g. FHIR, HL7v2, LOINC, SNOMED) for RIS digital products
    • Engage with internal key customers and stakeholders to understand their business needs, pain points using a customer-centric approach
    Online seit: 12.09.24
    Referenznummer: 781052/1

    Senior Expert Science & Technology – Functional Lead in Biologics – Global Drug Development (m/f/d)

    Basel Stadt
    • Independently design, plan, organize and perform scientific experiments for the preparation and timely delivery of biologic drug products (DP), processes and procedures
    • Independently design, plan, organize and perform specific analytical tests related to the experiments as well as for related stability studies
    • Documentation of raw data from the scientific experiments including all conducted analytical tests as well as evaluation. interpretation and reporting of all results of the scientific experiments together with the project responsible (Functional Lead)
    • Interprets results including drawing relevant conclusions and delivers respective work packages to meet agreed objectives & timelines in the project team. Ensures and drives information exchange in DP sub-team
    • You will be a core member of the Drug Product development sub-team, representing the scientific and technical excellence and you might be a member of the CMC team ad-hoc if required
    • Based on the project status, participate in function-specific project sub team meetings and discussions
    • If required, support the compilation of scientific protocols / reports and lab procedures based on existing templates as well as contribute to compilation of SOPs
    • Take over responsibility for specific tools / equipment and utilize special tools / equipment or specialized facilities as an expert
    • Schedule and perform maintenance and qualification of tools / instruments / equipment as needed
    • Develop new methods or optimize existing laboratory methods/processes as well as contribute to development and implementation of new technologies
    Online seit: 30.08.24
    Referenznummer: 780127/1

    QA Associate QMS (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Receives incoming documents e.g. executed batch records, work orders, vendor labels, packaging instructions etc.
    • Performs documentation in respective tools. Prepares documentation needed for the batch record review e.g. Analysis Reports, Specifications for clinical development, country label approval etc.
    • Support the timely release of GMP batches of labels, primary packed materials and Investigational Medical Products
    • Review and approve GMP relevant documents, e.g. work orders, packaging master documents, clinical study labels, Batch record review for both packed material from internal or contractors. Compiles, Notifications of Extension to be issued due to revised expiry dates. GMP relevant documents in own area of responsibility e.g. CoC's, BRR Checklists
    • Scan, file and archive documents owned by QA e.g. Certificate of Compliance, Batch Record Review Checklists
    • Write and review procedures and forms related to the QA Batch record Review Process
    • Contributes to Right First Time performance reports for release of IMPs
    • Supports and collaborates with QA & GCS Line Unit in process improvements, Quality & Compliance issues and in the use of GMP relevant IT tools and processes
    • Support the use, improvement, evaluation and implementation of GMP relevant IT tools and processes
    Online seit: 26.08.24
    Referenznummer: 779303/1

    Expert Science & Technology (Analytical Lab Technician) (m/f/d)

    Freelance/temporary employment for a project
    Basel City
    • We are looking for a highly motivated laboratory expert with the focus on development and optimization of analytical methods to control and monitor chemical manufacturing processes and products
    • Plan and perform development of analytical methods in a non-GMP environment
    • Utilize obtained analytical methods to generate data on development samples and prepare the method for transfer to a GMP lab. The focus of this position is on Mixed Modality technologies such as Radioligand Therapies, Antibody Drug Conjugates and Oligonucleotides
    • A key activity includes also the maintenance all relevant lab infrastructure and supports order and housekeeping of chemicals and reagents required
    Online seit: 21.08.24
    Referenznummer: 778863/1

    CQV Specialist (m/f/d)

    Freelance/temporary employment for a project
    Visp, Valais
    • Involved in all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others
    • Involved in the validation documentation including: URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ)
    • Prepare validation documents
    • Execution of IQ/OQ and PQ for equipment, systems and utilities
    • Write reports of completed validation activities. Work to identify efficiencies in the validation program approach
    • Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation
    • Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s
    • Write and/or revise procedures applicable to the Engineering activities
    • Support the Engineering group to prepare the validation, requalification, and maintenance program
    Online seit: 16.08.24
    Referenznummer: 778285/1

    PT KM Expert Sinequa / Search specialist (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Indexing and Content Management: Collaborate with data source owners and application owners to ensure that all relevant content is properly indexed and searchable in the context of a specific use case. This involves understanding business requirements, setting up indexing rules, and ensuring accurate and efficient content retrieval
    • Issue Monitoring and Troubleshooting: Monitor the search platform for any issues or anomalies and provide timely resolutions. Troubleshoot and resolve search-related issues, working closely with cross-functional teams and vendors if needed
    • Documentation and Best Practices: Develop and maintain documentation and best practices for the search platform, including configuration settings, indexing guidelines, troubleshooting procedures, and performance optimization techniques
    • Maintenance and Optimization: Regularly maintain and optimize the Sinequa search platform, ensuring it is up-to-date and performing at its best. This includes monitoring system health, implementing necessary upgrades and patches, and configuring platform settings for optimal performance
    Online seit: 14.08.24
    Referenznummer: 774908/1

    Global Project/Study Manager (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency and risk management
    • 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 comprehensivelabel 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. Develop and execute 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 amendment) to develop optimal supply strategy
    • Generates optimal distribution plans for investigational medicinal products (IMPs), jointly with partner functions. Triggers and tracks shipments of IMPs from central depot to regional hubs and local depots
    • Develops, maintains and executes an optimal resupply strategy with proactive planning, appropriate lead-time and replenishment quantities to ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies
    • Is responsible to consolidate, maintain and track the clinical trial budget with key stakeholders for overall GCS external cost (e.g. labels, packaging, distribution and comparators)
    Online seit: 24.07.24

    Sie möchten über relevante Jobangebote informiert werden?

    Referenznummer: 772087/1

    Master Production Scheduler DP (m/f/d)

    Freelance/temporary employment for a project
    Aargau
    • Drive optimization by proactively balancing demand priorities against optimal production and efficient resource utilization i.e. equipment, staff, materials, etc. within the respective Horizon.
    • Revise and maintain detailed planning and scheduling parameters i.e. calendars, productivity, utilization, fixed horizon etc. in the planning system to allow optimal use of system volume planning and detailed scheduling functionality.
    • Maintain an accurate production schedule, providing data for the MRP, Detailed Scheduling and Master Data processes to meet production demands.
    • Proactively communicate and resolve conflicts related to equipment capacity, staff capacity, materials requirements,etc.
    • Monitor production data, including volume, asset utilization, productivity, consumption of materials and quality control measures, using this information for Continuous Improvement activities and accuracy of planning parameters.
    • Revise, analyze and maintain planning parameters on a regular basis in the planning system to allow optimal use of system volume planning and detailed scheduling functionality.
    Online seit: 09.07.24
    Referenznummer: 768903/1

    Deployment DM Expert (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Serve as the deployment wave focal point for data objects within the migration/local data migration scope
    • Collaborate with Business Data Owners (BDOs), deployment Functional Experts, ETL team members, and legacy teams
    • Drive migration activities for deployment projects
    • Verify data transformation tools and outputs for deployment wave projects
    • Prepare and verify DMW load files
    • Execute DVT scripts
    • Coordinate defect resolution for assigned objects
    • Manage all aspects of data migration execution for global data migration scope
    • Align with functional experts on data-related topics
    • Design and test load programs for assigned objects
    Online seit: 21.06.24

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