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- ...assessments, risk assessment, cleaning documents, WI) ·Coordinate, review and approve quality... ...to, such as deviations, CAPAs, change controls, qualification and validation... ...experience in Quality Assurance or Quality Control in a manufacturing environment within Pharmaceutical...Empfohlen
- ...collaboration with Clinical Development stakeholders, overseeing documentation and quality control, and management of outsourced partners when applicable.... ...company standards ~Writes all trial Data Management documents covering specifications for external data transfer, data...Empfohlen
- ...products and their eventual commercial supply through a strong control strategy. Main Responsibilities: ~Serve as the Analytical SME... ...execution and alignment. ~Author, review, and approve critical documents and regulatory dossiers (e.g., QIMPD, NDA) while ensuring...EmpfohlenHomeoffice
- ...Pharmacy, at least 3 years of professional experience in Quality Control, and very good GMP knowledge. This role is a 12 months... ...appropriate GMP standard in the laboratory ~Scientific and regulatory documentation of the work done Qualifications and Experience: ·...Empfohlen
- ...possesses at least 3 years of professional experience in Quality Control, and has excellent GMP knowledge. Main Responsibilitis: ~... ...QA, Scientists, Senior Management) ~ Facilitation and Documentation of Root Cause Analyses ~ Active Participation in Quality Review...EmpfohlenHomeoffice
- ...trial programmer. ~Responsible for the review of trial documentation and providing feedback from statistical programming perspective... ...trial programmer and/or the statistician. ~Performs and documents quality control (QC) activities as per company standard operating...Empfohlen
- ...well as preparing detailed regulatory documentation for submission to health authorities.... ...Responsibilities: ~Developing a phase-appropriate control strategy for drug substances and drug... ...activities at CLOs/CDMOs ~Plan and document experiments/results independently and...EmpfohlenHomeoffice
- ...the electronic Trial Master File (eTMF) documents owned by Regulatory Affairs. The role ensures eTMF-relevant regulatory documentation is complete, accurate, timely, and compliant... .... ~Prepare and perform ongoing quality control (QC) of regulatory eTMF documents for...Empfohlen
- ...ordinators on Contract Basis in the Stucki area, Switzerland. Main Responsibilities: ~Perform all pull (retrieval, labelling and documentation) activities for stability studies. ~Login and receive samples in LIMS. Close collaboration with different departments. ~...Empfohlen
- ...Accounting & Controlling Trainee (a) Fliegen Sie mit uns in die Zukunft und werden Sie Teil des Teams bei einem der innovativsten Flugzeughersteller der Welt.Dauer: 18 Monate ACCOUNTING / CONTROLLING / FINANCE CONTROLLING & BUCHHALTUNG Ihr Arbeitsort: Stans, Switzerland...Empfohlen
- ...resolve issues and ensure leak-tight, contamination-free systems. ~Support commissioning and validation (IQ/OQ/PQ) for audit-ready documentation. Qualifications and Experience: ~Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required. ~At least 10...Empfohlen
- ...Business Unit Controller (a) Fliegen Sie mit uns in die Zukunft und werden Sie Teil des Teams bei einem der innovativsten Flugzeughersteller der Welt. ACCOUNTING / CONTROLLING / FINANCE GROUP CONTROLLING Ihr Arbeitsort: Stans, Switzerland Ihre Aufgaben Berichterstattung...Empfohlen
- ...simple maintenance, inspection, and supporting production work ~Execution of auxiliary work in the plant or maintenance area ~Documentation of completed work as instructed ~Compliance with safety and quality regulations (GMP) Your Profile ~Student (preferably with...EmpfohlenSommerjob
- (Junior) Project Controller 80-100% (a) Flieg mit uns in die Zukunft und werde Teil des Teams bei einem der innovativsten Flugzeughersteller der Welt.Als (Junior) Project Controller stellst du gemeinsam mit dem vierköpfigen Team die betriebswirtschaftliche Unterstützung...Empfohlen
- ...planning, conduct, data review, and reporting of Phase II and III clinical trials ·Authoring and co-authoring of key clinical trial documents, including protocols, ICFs, study committee charters, guidelines, and CSR ·Collaboration with other teams to develop, refine, or...Empfohlen
- ...Construction Managers for a 12-month position based in the Stein area, Switzerland. Main Responsibilities: ~Coordinate and control the service providers and suppliers, the individual work steps as well as the material flows. ~Manage all of the client’s owned works...
- ...security, and regulatory compliance requirements. ·Design and document upstream and downstream system interfaces. ·Partner with... ...defining configuration vs. customization strategies. ·Strong documentation skills, including architecture diagrams and workflow models (...
- ...Responsibilities: ~Operation, maintenance, and further development of the Oracle database landscape (RAC, ASM, Data Guard) ~Monitoring and control of systems using monitoring, alerting, and capacity management (OEM) ~Analysis and resolution of incidents as well as performance...
- ...The perfect candidate is a pragmatic, hands-on servant leader who thrives in ambiguity and leads by enabling the team rather than controlling them. He maintains a high-trust, psychologically safe environment while remaining firm on scope and commitments. Balancing a...
- ...investigation and rectification, testing, validation and certification of electrical system and components Develop system requirement documents and certification engineering reports Technical & program lead of electrical projects for both, new development and...
- ...definition, in-service problem investigation and rectification, system test, validation and certificationDevelop systems requirement documents and certification engineering reportsAct as primary point of contact for equipment suppliersTechnical and program lead of...
- ...Line and base maintenance on Pilatus aircraft, mainly Trainer aircraftPerformance of routine and non-routine tasks and accurate documentation of the work carried outEnsure full adherence to maintenance contracts, company and customer procedures to high quality standards...
- ...What you do Responsibility for test planning and implementation of new materials and processesCompilation and revision of technical documents, i.e. Process Specifications or Engineering StandardsProcessing requests and support to engineering, production as well as...
- ...future and become part of the team at one of the most innovative aircraft manufacturers in the world. ENGINEERING & TRAINING SYSTEMS DOCUMENTATION Your place of work: Stans, Switzerland What you do Conduct training need analysis to define the learning objectives and key...
- ...manufactured and externally sourced goods (commodities / software / technology / services) in compliance with all applicable export control regulationsExecuting sanctioned party screenings and / or embargo & sanctions verificationsMaintaining SAP GTS software as well as...
- ...mechanical systemsProven detailed experience in the fuel systemExperience in additional mechanical systems (e.g. powerplant, flight control, landing gear etc.) will be a plusExperience in component life cycle and proven strong vendor management skillsData analysis &...
- ...management (CM) by creating the engineering bill of material (EBOM) and manufacturing bill of material (MBOM)Write and review technical documentation part of the project/product lifecycle, such as technical specifications, system requirements and system design specifications...Temporär