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    Reference number: 780583/1

    Testmanager (m/f/d)

    Freelance/Contracting project
    North Rhine-Westphalia
    • Continuous improvement of software quality processes
    • Identification, documentation and reporting of quality defects
    • Promoting a proactive quality culture within the team
    • Participation in code reviews for early detection of quality issues
    • Develop effective testing strategies and perform manual and automated testing at various levels
    • Collaborate with various business teams to create relevant test cases
    • Executing test plans and scripts to validate software functionality
    • Understanding and familiarizing yourself with complex business processes and reducing process complexity
    • Supporting the team in the consideration of design and implementation decisions
    • Acting as a quality coach within the agile team 
    • Analysis, troubleshooting and problem solving
    • Teamwork with developers
    • Use of collaboration and tracking tools (Azure, DevOps)
    Online since: Thu Aug 29 13:21:55 CEST 2024
    Reference number: 779597/1

    Digital Sales Manager (m/f/d)

    Permanent employment with our customer
    Denmark
    • Drive digital sales success by negotiating contracts with current and potential customers in the metal casting segments
    • Spot new business opportunities and exploit them to the fullest with both current and new customers
    • Lead customer acquisition and support initiatives for the digital Monitizer products 
    • Foster strong, lasting relationships with customers, partners, and management
    • Meet and exceed your sales targets and revenue goals for Monitizer products
    • Support and train sales colleagues, representatives, and customers to ensure their success with our digital solutions
    Online since: Wed Aug 28 12:53:19 CEST 2024
    Reference number: 780419/1

    Scientist Immunology and Cardiovascular/Metabolic Disease (LSW) - BS (m/f/d)

    Freelance/temporary employment for a project
    Basel Stadt
    • Carefully design, organize, and manage externally run studies in collaboration with internal scientists, procurement and contract research organizations in a timely manner
    • Act as an advisor for study design: Define scientific rationale, success metrics and monitor progress
    • Provide high quality analysis of conducted studies and summarize, present and discuss study results with project teams
    • Ensure excellent interaction with vendors and maintain overview on activities and capabilities of relevant CROs
    • Work on a flexible schedule to meet deadlines
    Online since: Tue Aug 27 11:29:41 CEST 2024
    Reference number: 780194/1

    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
    • Represents 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
    • Maintains 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
    • Ensures timely escalation of potential technical, compliance or safety issues to the MS&T team and partners with internal MS&T resources to remediate
    • Ensures 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: Mon Aug 26 14:29:30 CEST 2024
    Reference number: 778924/1

    Area Sales Manager (m/f/d)

    Permanent employment with our customer
    Denmark
    As an EssilorLuxottica Area Sales Manager covering all lenses distribution in Denmark, you are responsible for the delivery of targeted sales for your products for your territory, including follow-up, training of customers and campaign launches assigned to the Area Manager’s portfolio. All tasks must be completed in compliance with the framework and agreements that exist between the customer/chain and the Company:
    • Main responsibility for sales and development of sales, information, follow-up and training in EssilorLuxottica products during agreed store visits. 
    • Build relationships with existing customer base and support them throughout all life cycles. 
    • Independently identify market and customer potential through analysis of the customer, market and competitive structure. 
    • Responsibility for the success-oriented development of our market position and our customers in North Europe. 
    • Stay abreast of market changes / trends as well as competitors within the industry. 
    • Proactively acquire new customers. 
    • Represent our fast-growing company at trade fairs and events. 
    • Represent EssilorLuxottica in a positive way according to normal business practice and ethics. 
    • Weekend work must be expected in connection with trade fairs, meetings or other activities, approximately 4-5 weekends per year. 
    • Reporting weekly visits according to agreed targets. 
    • Bring energy to colleagues and contribute to creating a world class team.
    Online since: Mon Aug 26 10:15:30 CEST 2024
    Reference number: 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 since: Mon Aug 26 09:40:22 CEST 2024
    Reference number: 780106/1

    Biotechnologist (m/f/d)

    Freelance/temporary employment for a project
    Visp, Valais, Switzerland
    • Executes manufacturing activities in the area of Drug Product according to cGMP guidelines, ensuring batch execution, evaluating test results, resolving issues, troubleshoot manufacturing equipment and make recommendations for resolution.
    • Provides front line technical and procedural support, working with the manufacturing team.
    • Securing each batch is manufactured safely, on time, in compliance with the batch instructions and quality requirements
    • Responsible for establishing timely and with high quality the required production documentation (preparation, execution and review of batch records) or other relevant GMP documents for the assigned production area.
    • Supports process related investigations and assists in decision making?on production issues
    • Supports process changes and CAPAs related to processes within required timelines
    • Performs training activities of relevant areas as operator and supports others and new joiners.
    • Operating, setting up and cleaning production equipment and premises for the production of liquid and freeze-dried drug forms (e.g.:compounding, parts washing, autoclaving, filter integrity testing, visual inspection)
    Online since: Fri Aug 23 16:57:39 CEST 2024
    Reference number: 779854/1

    AWS Cloud Platform & Fullstack Developer (m/f/d)

    Freelance/Contracting project
    Baden-Wurttemberg
    • Development in Micro-Service-Architecture and Cloud-Architecture
    • AWS Cloud Development and CI/CD, ECS / Fargate, Lambda, Redis, CloudFront, S3, Route53, Github Actions
    • Development with Infrastructure as code tools, especially Terraform
    • Work on / built-up infrastructure and applications running in the cloud 
    • Implementing backend applications and APIs
    • Handle API Management with Apigee
    • Refine features
    • Develop technical solutions based on defined requirements and user stories
    • Consult product owner and other ART stakeholder in solution design/ concepts
    • Develop/ code solutions
    • Perform code reviews
    • Support test concept development, end-to-end integration tests
    • Develop automated test routines
    • Document solutions
    Online since: Thu Aug 22 14:19:36 CEST 2024
    Reference number: 779130/1

    Client Operations Onboarding, Maintenance, Quality Control Analyst (m/f/d)

    Freelance/temporary employment for a project
    Geneva
    • Process new account opening requests in a timely and efficient manner, with the highest standards of quality and care. Ensure the business is compliant with all Bank policies and global regulatory / legal requirements 
    • Perform documentation updates for existing clients within the agreed timeframes 
    • Enter data into various databases and check to ensure the accuracy of the data inputted 
    • Perform quality reviews of new account openings and KYC periodic reviews in a timely and efficient manner, with the highest standards of quality and care 
    • Prepare client KYC analyses, interacting with the Bankers to obtain KYC and other compliance information and documentation 
    • Perform remediation exercises as requested, including remediation of digital and physical records 
    • Follow up on all outstanding issues / escalations with relevant partners in the Bank including
    • Risk / Controls team and ensure a good relationship with key stakeholders to ensure the best client experience
    Online since: Thu Aug 22 14:16:05 CEST 2024
    Reference number: 779690/1

    Drupal Developer (m/f/d)

    Freelance/temporary employment for a project
    Bern and Remote
    • Collaborate with the development team to implement challenging and high-quality projects using Drupal 10
    • Take responsibility for the architecture and implementation of modular and reusable extensions
    • Work with the open-source community to improve our own modules as well as third-party modules
    • Support customer projects, support requests, and updates as part of a project team
    • Experience integration, deployment, and automated testing as part of software development
    Online since: Thu Aug 22 11:44:12 CEST 2024

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    Reference number: 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 since: Wed Aug 21 16:18:41 CEST 2024
    Reference number: 779339/1

    Senior Scientist Validation (m/f/d)

    Freelance/temporary employment for a project
    Neuchatel
    • Develop, implement and manage the site process validation, and revalidation strategies to meet cGMP and quality requirements on time and on budget to ensure that programs are compliant with Regulatory Authorities’ expectations and related SOPs
    • Collaborate with cross functional teams to define the interfaces to equipment qualification / utilities qualification, system qualification and analytical method validation.
    • Establish and maintain the Validation Master Plan for process validation. Ensure that all manufacturing processes are validated, overview on state of validation at site is maintained.
    • Participate in transfers and launches, liaise with technical development for new products and align on the product validation approach. Contribute to provide experimental data obtained during the validation activities, which will be used to prepare the related registration documentation
    • Author or reviewer for routine validation protocols and reports, associated change controls and supports the execution at the shop floor
    • Develop the strategy for continued process verification that ensures all critical process parameters and quality attributes are monitored or analysed, and actions are defined and taken in case of trends or deviations. Reviews plans for CPV
    • Lead and drive investigation for validation related matters and implement corrective and preventive actions
    • Contribute to all relevant audit inspection and ensure inspection readiness for the site. Ensure compliance with relevant regulatory requirement, GMP, and other industry standards
    • Initiate, drive and implement continuous improvement initiatives to optimize processes, enhance produce performance and drive operational excellence for better quality, safety and efficiency
    Online since: Wed Aug 21 16:05:05 CEST 2024
    Reference number: 743269/1

    Laboratory Analyst / Lab Technician (m/f/d)

    Freelance/temporary employment for a project
    Neuchatel
    • Perform analytical chemistry testing that is required for release of drug products, stability samples and raw materials. Additional responsibilities may include support to analytical method transfers and validations, stability studies, revision of documents, handling of deviations and implementation of change controls
    • As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory
    • Performs analytical testing of solid oral drug products for release and stability testing, HPLC / UPLC, GC, UV/VIS, dissolution, etc.
    • Performs associated laboratory work preparation of solutions, waste disposal, etc.
    • Supports testing of raw materials according to pharmacopeia requirements
    • Performs peer review of analytical data
    • Respects EHS rules at all time
    • Respects 5S principles and proposes ideas for continuous improvement to lab processes
    • Can be assigned special tasks and project work
    Online since: Wed Aug 21 15:41:57 CEST 2024
    Reference number: 778328/1

    SAP Consultant (m/f/d)

    Freelance/temporary employment for a project
    Winterthur
    • Verantwortung über SAP FICO 4 Hana-Module
    • Koordination von Tickets, Changes und Anfragen mit externen Partnern
    • Aufbau und Koordination der Infrastruktur für MM-/SD-Module
    • Dokumentation und Sicherstellung der Tracability von Changes
    • SAP-Optimierung in Zusammenarbeit mit externen Partnern
    • Erstellung von Reports und Analysen
    Online since: Wed Aug 21 11:24:42 CEST 2024
    Reference number: 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 since: Fri Aug 16 17:00:18 CEST 2024
    Reference number: 778889/1

    Scientist Product Characterization (m/f/d)

    Employment with Hays Professional Solutions GmbH
    Marburg
    • Develop and qualify robust, fit-for-purpose analytical mass-spectrometry methods and optimize existing LC-MS and LC-MS/MS methods to support development activities of Recombinant Product Development
    • Execute method development, qualification and/or optimization studies following QbD principles where applicable
    • Prepare assay test procedures and assay qualification protocols for new test methods for approval by a Senior Scientist/Manager (e.g. peptide mapping, intact mass and middle down)
    • Plan and execute analytical studies/ routine MS-analyses to support process development activities, product comparison and physico-chemical characterization activities (e.g. Comparability Studies, Forced Degradation Studies)
    • When required perform routine analysis of samples using assays such as (but not limited to) SDS-PAGE, Western Blots, HPLC based assays (e.g. SE-HPLC, RP-HPLC, AIX-HPLC), glyco-profiling
    • Prepare scientific reports detailing assay development and qualification studies or other analytical studies and present analytical data to key stakeholders
    • Implement and support quality systems within the group and ensure department compliance with scientific standards
    • Support the maintenance of laboratory and analytical equipment. Liaise with instrument engineers and/or external service providers for maintenance of equipment
    • Participate in the selection of equipment for purchase, write user requirements and prepare purchase orders
    • Follow safety standards as governed by local, state and federal regulations, laws and policies as well as companiy policies and directives.
    Online since: Fri Aug 16 14:17:17 CEST 2024
    Reference number: 768761/1

    Senior Fullstack Developer (m/f/d)

    Permanent employment with our customer
    Hamburg
    • Design and deploy innovative features for the Sellers Center to enhance the online retail experience
    • Collaborate with product managers, UI/UX designers, and fellow engineers to brainstorm and create effective solutions
    • Utilize the SCAYLE platform to manage product and order information efficiently
    • Enhance application performance through strategic SQL Query optimizations
    • Engage in code reviews to uphold high standards of code quality and foster ongoing improvement
    • Offer technical support, and troubleshooting issues to ensure consistency
    Online since: Thu Aug 15 19:51:33 CEST 2024
    Reference number: 778450/1

    Business Development Manager – Services (m/f/d)

    Freelance/temporary employment for a project
    Zug
    • Acquisition of new customers in the area of IT services for enterprise customers
    • Building and maintaining trusting business relationships
    • Conducting successful first contact sales meetings
    • Technical understanding of the customer's requirements and the ability to understand and explain technical aspects
    • Working with project-oriented teams in one or more areas of expertise such as Data Warehouse, Data Lakehouse, Data Platform, Data Engineering, Azure Databricks, Microsoft 365 or Microsoft Dynamics 365 Sales
    Online since: Wed Aug 14 14:57:39 CEST 2024
    Reference number: 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 since: Wed Aug 14 11:21:03 CEST 2024
    Reference number: 778218/1

    Electrical Lead Engineer (m/f/d)

    Freelance/temporary employment for a project
    Zurich
    • Requirements definition at electronics board level
    • Detailed design including trade-off, analysis, schematics capturing
    • Verification of electrical circuits by review, analysis and simulation
    • Coordination of Unit Interface Equipment (UIE) / EGSE definition and commissioning
    • Prototype and Flight electronics commissioning and testing
    • Assembly, Integration and Testing (AIT) support
    • Control and monitor the team mates in PCB/CCA domain
    • Ensure process adherence in the electronics development
    • Timely reporting/flagging to team leaders
    • Preliminary internal design reviews (schematics, layout, manufacturing files), checkpoint to release for project review teamEstablish and maintain engineering plans and activities schedules (e.g. in MS Project)
    • Coordination of a small team of development engineers 
    Online since: Tue Aug 13 16:49:50 CEST 2024
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