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- ...get the right therapies in the right doses at the right time - a concept that we internally adopt as "There is a Patient Waiting." Our... ...Provide input into User Requirement Specifications of Interactive Response Technology (IRT) medication management module and complete User...SuggéréTravail à distanceTemps pleinRemote job
- ...Nous recherchons pour l'un de nos clients un Responsable achats Responsabilités ~ Définir et mettre en œuvre la stratégie achats de l'entreprise. ~Identifier, sélectionner et négocier avec les fournisseurs. ~Gérer les appels d'offres et analyser les propositions...Suggéré
- ...teams to ensure data integrity, patient safety, regulatory compliance, and inspection readiness throughout trial execution. Responsibilities Identify, assess, and advise on mitigation of quality risks affecting trial data integrity and patient safety Lead...Suggéré
- ...Responsibilities Lead statistical strategy for real-world evidence and health outcomes studies across departments Develop protocols, statistical analysis plans, and study reports ensuring scientific rigor Recommend optimal study designs leveraging administrative...Suggéré
- ...overseeing timely delivery, budget management, and cross-functional collaboration while serving as primary client contact. Responsibilities Manage end-to-end project coordination including study specifications, timelines, budgets, and documentation Foster communication...Suggéré
- ...compliance with regulatory guidelines and managing inventory systems. Standard Monday-Friday schedule in warehouse environment. Responsibilities Receive goods and post receipts in GPMS system; coordinate shipment handover to freight carriers Perform high-bay...Suggéré
- ...making sure our food is safe or helping find cures for cancer. Position Summary The Goods Receipt Specialist in Allschwil is responsible for the timely receipt, booking, and storage of materials. The role records deviations in the TrackWise system and supports...SuggéréTravail à distanceTemps plein
- ...Senior Quality Control Technician role at a pharmaceutical manufacturing facility responsible for ensuring compliance with GMP standards through inspection, monitoring, and documentation of production processes and materials in a cleanroom environment. Responsibilities...SuggéréTravail posté
- ...Zuverlässigkeit und die Verfügbarkeit seiner ICT-Umgebung zu erhöhen.Wir suchen zur Verstärkung unseres Cyber Security Incident Response Teams in Spreitenbach AG, Tagelswangen ZH oder Reinach BL eine initiative und kommunikative Persönlichkeit als Incident...SuggéréActivité indépendanteTravail de vacancesTravail à domicile
- ...PPE when needed Proficiency with Microsoft Office Suite applications Demonstrates commitment to company values of Integrity, Intensity, Innovation and Involvement Shift work and on-call responsibilities may be required Travel up to 20% may be required...SuggéréTravail à distanceTemps pleinTravail posté
- ...manages data standards programs, and serves as a key point of contact across clinical, statistical, and regulatory teams. Responsibilities Provide expert guidance on regulatory submission requirements and industry standards documentation Serve as point of contact...Suggéré
- ...ambient, refrigerated, and frozen shipments for global delivery while maintaining GMP/GDP compliance and quality standards. Responsibilities Process and prioritize daily standardized shipping orders independently Pick and pack complex clinical trial materials...Suggéré
- ...regulatory compliance for pharmaceutical and biotech clients. Responsibilities Design and implement inventory management plans to... ...trial drug supply globally Review and optimize Interactive Response Technology settings to support supply and demand strategy...Suggéré
- ...ensure GMP compliance, and coordinate cross-functional teams to meet safety, quality, delivery, and financial objectives. Responsibilities Direct strategic and daily operations of manufacturing, packaging, and warehouse functions Ensure compliance with GMP standards...Suggéré
- ...Responsibilities Direct Phase 1-3 clinical trials and develop study protocols aligned with company procedures Lead selection of clinical investigators and manage ongoing investigator relationships Assess adverse events and evaluate safety of compounds throughout...Suggéré
- ...functional activities from study setup through completion while serving as the primary point of contact for clients. Your responsibilities: • Manage end-to-end project coordination, including study specifications, timeline development, budget management, and...Travail à distanceTemps plein
- ...project coordination, documentation management, and stakeholder communication within a regulated manufacturing environment. Responsibilities Coordinate clinical trial project activities and manage associated documentation Support supply chain operations and...
- ...Senior manufacturing equipment maintenance technician at a pharmaceutical facility responsible for timely setup, maintenance, calibration, and repair of production equipment. The role requires independent work within GMP and regulatory guidelines, technical support to...Travail posté
- ...regulations. They develop improvement proposals and always communicate proactively and in a solution-oriented manner. The mechanic is responsible for the timely changeover/setup of machines as well as technical support of Operations during order execution. They are...Travail à distanceTemps pleinTravail posté
- ...expertise, you will identify new opportunities, shape market strategies, and support profitable growth across global markets. Your Responsibilities Drive business development activities across Industrial Testing markets, owning market analysis, identifying and converting...Temps plein
- ...Responsibilities Develop clinical QA strategy and establish stakeholder relationships to achieve GCP compliance Build and lead quality management team to implement systems and ensure study compliance Lead preparations for regulatory inspections including mock...
- ...Responsibilities Lead regulatory strategy and execution across product lifecycle for therapeutic area programs Represent regulatory perspective at therapeutic area and enterprise governance forums Provide strategic oversight and hands-on execution for programs...
CHF 90000 - CHF 115000 par année
...Nous recherchons un(e) Responsable Ingénierie de Production – Usinage de Précision pour rejoindre un acteur industriel suisse reconnu, évoluant dans un environnement technique exigeant et orienté haute précision. Vous occuperez un rôle clé dans l’amélioration des performances...- ...project leadership, focusing on automation, process improvement, and adoption of cutting-edge tools across global operations. Responsibilities Lead technical strategy and innovation initiatives within Clinical and Statistical Programming functional area Identify,...
- ...the PM client portfolio to ensure successful completion and supply maintenance over the life cycle of each project. Key Responsibilities: Partners with the internal project management team to help support the success of a study in any way possible. Assists...Travail à distanceTemps plein
- ...Responsibilities Develop clinical pharmacology and quantitative strategies for assigned therapeutic areas supporting development decisions Oversee pharmacokinetic and pharmacodynamic activities for clinical development compounds across portfolio Provide small...
- ...leadership, client portfolio oversight, and process improvement to ensure timely project delivery and customer satisfaction. Responsibilities Develop, mentor, and evaluate project managers and support staff; implement performance improvement plans Direct project...
- ...health data across multiple functions and geographies, establishing standardized metadata and discoverable data inventories. Responsibilities Lead EHDS Data Inventory and Cataloguing workstream; coordinate data owners to identify in-scope datasets and holdings...
- ...Fisher Scientific in Allschwil. The Senior Project Manager, Client Services Distribution leads all aspects of leadership and is responsible for the actions of project managers and project support associates. You will work closely to guarantee the timely and flawless delivery...Travail à distanceTemps plein
- ...Leader position overseeing in-process inspection operations within a press manufacturing environment at a life-science company. Responsibilities include leading inspection teams, ensuring GMP compliance, coordinating cross-functional activities, and driving continuous...Travail posté