Jobsuche und Projektbörse für Fach- und Führungskräfte

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724 Ergebnisse

Senior Electrical Engineer (m/f/d)

Freelance/temporary employment for a project

Rotkreuz

Collaborate in a diverse and interdisciplinary team of electronics, mechanics, optics and software experts participate in defining work packages, their effort estimation, planning and implementation within the development team
Execute work packages with respect to budget, timeline, scope and quality
Develop PCBAs, firmware, wirings and cables for diagnostic systems (eCAD, Microcontroller programming) based on technical requirements including design verification and maintenance
Write or contribute to concepts and specifications, risk management, verification and validation as well as technical investigations
Analyze technical problems and elaborate solution proposals
Support product hand-over from development to production towards launch and beyond
Co-author relevant documentation based on the development process

Online seit: Thu Sep 26 14:57:45 CEST 2024

Senior C-Cure Developer (m/f/d)

Freelance/temporary employment for a project

Remote

Implementation of the internal customer application system into the Johnson Library Control System
Programming and development of the architecture for the specific control system (adapter)
Consulting and supporting the customer with technical questions
Participation in a large customer implementation project

Online seit: Wed Sep 25 14:06:56 CEST 2024

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: Fri Sep 20 15:09:36 CEST 2024

MSAT Product & Process Engineer (m/f/d)

Freelance/temporary employment for a project

Rotkreuz

Continuous Improvement Tasks within the sensor production process (screen printing, dispensing, chemistry lab and materials)
Scientific Root Cause Analysis and problem solving
Support with establishing new production lines and processes

Online seit: Thu Sep 19 13:39:37 CEST 2024

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: Thu Sep 19 13:37:59 CEST 2024

CSV Specialist (m/f/d)

Freelance/temporary employment for a project

Neuchatel

Support and interface with process owners of systems and take part in daily activities upon request (provide technical and statistical support)
Execute and documents Equipment & Software validation
Oversee validation and qualification activities executed by analysts, provide training and support
Ensure cGMP compliant and timely implementation and maintenance of validated status of systems
Conduct/participate in risk assessments, root cause analysis and investigations
Identify, lead and drive improvements or change
Provide technical assessments on protocols deviations and investigations
Serve as SME for internal technical group discussions

Online seit: Thu Sep 19 13:27:24 CEST 2024

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: Thu Sep 12 10:59:27 CEST 2024

Senior ServiceNow Developer and Implementation Specialist (m/f/d)

Freelance/temporary employment for a project

Geneva

Design ServiceNow solutions that align with business goals and processes
Develop, configure, and improve core and custom applications and work directly with end users to resolve support issues
Configure and customize ServiceNow applications and modules
Develop workflows, business rules, UI policies, client scripts, and other customizations
Integrate ServiceNow with other enterprise systems and third-party applications
Utilize APIs, web services, and middleware tools for seamless integration
Implement and deploy ServiceNow solutions in various on prem environments (development, testing, production)
Conduct and support unit testing, system testing, and user acceptance testing (UAT). Expand and promote ATF
Create and maintain comprehensive documentation, including design documents, configuration guides, and user manuals
Monitor and maintain ServiceNow instances post-implementation

Online seit: Wed Sep 11 14:58:00 CEST 2024

Senior Group Technical Accounting and Reporting Specialist (m/f/d)

Freelance/temporary employment for a project

Baden

Responsible for operational execution and processes, including definition of the standards and policies for A&R, validation and processing of subsidiaries’ inputs and preparation of Group public reports
Subject matter expert on specific A&R topics including, but not limited to, restructuring, revenue recognition, inventories and provisions for industrial companies
Researching on technical accounting matters and preparing technical accounting memos for internal stakeholders and the external auditors
Leading role in group-wide projects with focus on accounting, A&R including the implementation of updates to US GAAP standards
Organizing and facilitating internal and external training on accounting and reporting related matters
Designing and maintaining internal controls over financial reporting and performing control activities in the respective area of responsibility in compliance with Sarbanes-Oxley requirements
First point of contact for the group external auditor

Online seit: Wed Sep 11 13:33:07 CEST 2024

Requirement and Test Automation Engineer 100% (m/f/d)

Freelance/temporary employment for a project

Zurich

You work autonomously in an Agile team and in continuous improvement spirit
You collaborate with the systems end users and other teams to understand business needs and functional specifications
You read and understand regulation rules and quality level that the products need to comply with
You read and understand Functional System Requirements provided by the Business Analyst
You write, review, and update the Equipment Requirements and perform the traceability to the Functional System Requirements
You can create and maintain some test cases providing coverage of Equipment Requirements
You review and test against the Software Requirements Specification and establish test traceability
You create and maintain automated tests using Python and Java Custom Junit frameworks using JAVA are advantageous
You execute manual and automatic tests and report results and describe issues/bugs in the issues Database
You synchronize and update the Test Results Management tool and perform formal system tests (Factory Acceptance Test)

Online seit: Thu Sep 05 15:38:23 CEST 2024

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Commissioning Engineer (m/f/d)

Freelance/temporary employment for a project

Aargau

Provide assistance in the commissioning and qualification of the following utility and process systems 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
Execute and Review Commissioning and Qualification test protocols (using KNEAT electronic documentation system)
Support the integrated commissioning of the DeltaV system software, hardware and interfaces to the various process and utility systems listed above
Support the reliable operation of the various automated systems by providing hands on engineering support to troubleshoot control system process control and operational issues
Support the overall Project Team to collate supporting information to allow timely decisions to be made that will minimize cost, timeline and quality impact on the Project
Guiding and supporting field execution ensuring that all equipment is commissioned according to standards and procedure and in line with cGMP
To ensure that any issues found are documented through KNEAT and raising project changes as required to ensure resolutions can be implemented in a timely manner
Provides coaching and training to team members to develop overall team knowledge to ensure fast track commissioning can be achieved
Ensures C&Q field execution is completed in a safe manner and following HSE standards, this will include overall oversight of Lock-Out-Tag-Out preparation, RAMSpreparation, PSHR completion, Method Statements, and Start-up activities

Online seit: Wed Sep 04 16:07:13 CEST 2024

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: Fri Aug 30 13:21:55 CEST 2024

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 seit: Tue Aug 27 11:29:41 CEST 2024

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 seit: Mon Aug 26 14:29:30 CEST 2024

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: Mon Aug 26 09:40:22 CEST 2024

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 seit: Fri Aug 23 16:57:39 CEST 2024

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 seit: Thu Aug 22 14:16:05 CEST 2024

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: Wed Aug 21 16:18:41 CEST 2024

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 seit: Wed Aug 21 16:05:05 CEST 2024

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 seit: Wed Aug 21 15:41:57 CEST 2024

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