23 jobs found in neuchatel, neuchatel

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    • neuchâtel, neuchâtel
    • temporary
    For our client Philip Morris SA in Neuchâtel, we are seeking an :Laboratory TechnicianInitiale duration : 6 monthsPerform laboratory tests in order to generate accurate data on aerosol collection to support routine, special projects, method development and/or proficiency test studies.Maintain and basic troubleshoot simple and medium complexity aerosol equipment to ensure business continuity. Ensure sufficient quantities of supplies for continuous laboratory operation.Complete short term activities of a repetitive nature with a high level of quality and apply standard operating procedures and work instructions as instructed to support lab activities.Perform knowledge management via data compilation, review and storage in line with Company, ISO or any other equivalent accreditation authority requirementsAdhere to all EHS rules, policies and procedures.Perform his/her duties in accordance to Good Laboratory Practices (GLP) regulations when applicable, ISO 17025 and the respective PMI procedures and ensure that processes, documents and activities within team, comply with ISO 17025.Carry out all of the activities ensuring that PMI Compliance Policies, standards, and laws relating to these activities are fully respected, integrated and understood by stakeholders, and apply adequate processes to ensure the protection of information of a confidential nature.
    For our client Philip Morris SA in Neuchâtel, we are seeking an :Laboratory TechnicianInitiale duration : 6 monthsPerform laboratory tests in order to generate accurate data on aerosol collection to support routine, special projects, method development and/or proficiency test studies.Maintain and basic troubleshoot simple and medium complexity aerosol equipment to ensure business continuity. Ensure sufficient quantities of supplies for continuous laboratory operation.Complete short term activities of a repetitive nature with a high level of quality and apply standard operating procedures and work instructions as instructed to support lab activities.Perform knowledge management via data compilation, review and storage in line with Company, ISO or any other equivalent accreditation authority requirementsAdhere to all EHS rules, policies and procedures.Perform his/her duties in accordance to Good Laboratory Practices (GLP) regulations when applicable, ISO 17025 and the respective PMI procedures and ensure that processes, documents and activities within team, comply with ISO 17025.Carry out all of the activities ensuring that PMI Compliance Policies, standards, and laws relating to these activities are fully respected, integrated and understood by stakeholders, and apply adequate processes to ensure the protection of information of a confidential nature.
    • neuchâtel, neuchâtel
    • temporary
    Hallo! Es-tu à la recherche d'une opportunitée dans une entreprise qui se soucie de la transparence et la communication? Sie sprechen perfekt deutsch et Français ? Super, j'ai une bonne nouvelle à t'annoncer ! Nous sommes à la recherche d'une personne parfaitement Bilingue FRA/ALL pour occuper un poste de : Collaborateur au service client à 100% (H/F)
    Hallo! Es-tu à la recherche d'une opportunitée dans une entreprise qui se soucie de la transparence et la communication? Sie sprechen perfekt deutsch et Français ? Super, j'ai une bonne nouvelle à t'annoncer ! Nous sommes à la recherche d'une personne parfaitement Bilingue FRA/ALL pour occuper un poste de : Collaborateur au service client à 100% (H/F)
    • neuchâtel, neuchâtel
    • temporary
    Pour notre client Philip Morris, nous sommes à la recherche d'un : Technicien MDC Durée : indéterminée Si vous êtes désireux de travailler dans un environnement de travail en constante évolution et toujours prêt à relever de nouveaux défis, vous êtes celui que nous souhaitons dans notre équipe Prototypage au MDC Neuchâtel.En tant que technicien, vous planifiez, gérez et conduisez la production de prototypes de substrats avec une équipe d'opérateurs. Vous soutenez également les innovations de processus liées aux substrats et établissez des procédures pour faire fonctionner la production. Vos responsabilités:Donner du support à nos partenaires pour la définition et l'exécution des plans d'expériencePlanifier, gérer et conduire les productions de prototypes en fonction des demandes et contraintes des chefs de projetsSuivre les processus et proposer des améliorationsParticiper à la mise en place de solutions pour améliorer la qualité et l'efficacité des équipements et des processus.Assurer une bonne gestion des informations et de la documentationGérer les maintenances préventives des équipementsAppliquer toutes les règles et procédures en matière de qualité, d'environnement, de santé et de sécurité conformément à la législation et aux standards de l'entreprise.
    Pour notre client Philip Morris, nous sommes à la recherche d'un : Technicien MDC Durée : indéterminée Si vous êtes désireux de travailler dans un environnement de travail en constante évolution et toujours prêt à relever de nouveaux défis, vous êtes celui que nous souhaitons dans notre équipe Prototypage au MDC Neuchâtel.En tant que technicien, vous planifiez, gérez et conduisez la production de prototypes de substrats avec une équipe d'opérateurs. Vous soutenez également les innovations de processus liées aux substrats et établissez des procédures pour faire fonctionner la production. Vos responsabilités:Donner du support à nos partenaires pour la définition et l'exécution des plans d'expériencePlanifier, gérer et conduire les productions de prototypes en fonction des demandes et contraintes des chefs de projetsSuivre les processus et proposer des améliorationsParticiper à la mise en place de solutions pour améliorer la qualité et l'efficacité des équipements et des processus.Assurer une bonne gestion des informations et de la documentationGérer les maintenances préventives des équipementsAppliquer toutes les règles et procédures en matière de qualité, d'environnement, de santé et de sécurité conformément à la législation et aux standards de l'entreprise.
    • neuchâtel, neuchâtel
    • temporary
    Nous sommes activement à la recherche, pour l'un de nos clients sur le bas du canton de Neuchâtel, d'un/e:Chauffeur poids lourds avec permis CE à 100% (H/F)Pour une mission temporaire du 28.09.2020 à 31.12.2020
    Nous sommes activement à la recherche, pour l'un de nos clients sur le bas du canton de Neuchâtel, d'un/e:Chauffeur poids lourds avec permis CE à 100% (H/F)Pour une mission temporaire du 28.09.2020 à 31.12.2020
    • neuchâtel, neuchâtel
    • temporary
    Randstad Professionals is currently looking for a Project Leader - Vision who will be assigned an interesting challenge for a major client working in the tobacco industry in Neuchatel:Contract: 6 months with possibility of extensionPurpose of the job:Lead projects related to testing equipment design, manufacturing as well as method development and qualification stages to assess and control Reduced Risk Products quality.Accountabilities:Develop new technologies & solutions for testing quality parameters of novel RRPs and its componentManage multiple projects from the stage of proof of concept up to designing and manufacturing high throughput testing equipmentDevelop, plan, execute and qualify/validate test equipment and its methodsInitiate and build up collaborations with external centers of expertise (universities, suppliers, laboratories, etc.)Qualifications:University degree in Engineering, Computer Science, Material Science, PhysicsExperience in project and people (direct/indirect) management is mustExperience in vision system and image analysis software is mustExperience in non-destructive testing technologies is preferred.Experience in machine learning, deep learning is preferred.Metrology knowledge, developing new test methods for sophisticated consumer goods is plusExperience in mechatronics and robotics is a plus.Experience in automation & pharmaceutical standards is plusFluency in English, both oral and written are must. French is a plus.OK to travel up to 20% Skills / Competencies:Leadership, communication, drive, action oriented, planningAbility to deal with ambiguity, collaboration, teamwork, consumer focus, creativity Please note a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position. 
    Randstad Professionals is currently looking for a Project Leader - Vision who will be assigned an interesting challenge for a major client working in the tobacco industry in Neuchatel:Contract: 6 months with possibility of extensionPurpose of the job:Lead projects related to testing equipment design, manufacturing as well as method development and qualification stages to assess and control Reduced Risk Products quality.Accountabilities:Develop new technologies & solutions for testing quality parameters of novel RRPs and its componentManage multiple projects from the stage of proof of concept up to designing and manufacturing high throughput testing equipmentDevelop, plan, execute and qualify/validate test equipment and its methodsInitiate and build up collaborations with external centers of expertise (universities, suppliers, laboratories, etc.)Qualifications:University degree in Engineering, Computer Science, Material Science, PhysicsExperience in project and people (direct/indirect) management is mustExperience in vision system and image analysis software is mustExperience in non-destructive testing technologies is preferred.Experience in machine learning, deep learning is preferred.Metrology knowledge, developing new test methods for sophisticated consumer goods is plusExperience in mechatronics and robotics is a plus.Experience in automation & pharmaceutical standards is plusFluency in English, both oral and written are must. French is a plus.OK to travel up to 20% Skills / Competencies:Leadership, communication, drive, action oriented, planningAbility to deal with ambiguity, collaboration, teamwork, consumer focus, creativity Please note a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position. 
    • neuchâtel, neuchâtel
    • temporary
    For our client Philip Morris SA in Neuchâtel, we are seeking an :CSV Engineer : Computer system validation Initiale duration : 6 months Lead computerized system validation project approach. Participation inthe establishment of validation strategy of computerized system and QAreview all documentation produced by the project SME. Maintain and insure proper validation state of system within his scope of competency. Ensure training of project team members and users of the system regarding validation and data integrity. Insure that projects plan and change management activities are properly scheduled and are adequately staffed. Participate in the creation and maintenance of the risk assessments (Project and Change) Validation Plan and Validation Report of new and existing system. Ensure that all validation activities are carried out, reported and closed according to plan provided by the Validation Lead. Perform QA Review of SME documentation produced to support the system validation. Participate in the development and improvement of QMS procedures and practices for data integrity and CSV as it relates to the area of responsibility.Advice project manager and service manager for validation activities and workload to ensure proper planning and workforce mobilization to perform the activities. Train and coach on the validation and data integrity strategy and practices as well as practices related to CSV and data integrity.
    For our client Philip Morris SA in Neuchâtel, we are seeking an :CSV Engineer : Computer system validation Initiale duration : 6 months Lead computerized system validation project approach. Participation inthe establishment of validation strategy of computerized system and QAreview all documentation produced by the project SME. Maintain and insure proper validation state of system within his scope of competency. Ensure training of project team members and users of the system regarding validation and data integrity. Insure that projects plan and change management activities are properly scheduled and are adequately staffed. Participate in the creation and maintenance of the risk assessments (Project and Change) Validation Plan and Validation Report of new and existing system. Ensure that all validation activities are carried out, reported and closed according to plan provided by the Validation Lead. Perform QA Review of SME documentation produced to support the system validation. Participate in the development and improvement of QMS procedures and practices for data integrity and CSV as it relates to the area of responsibility.Advice project manager and service manager for validation activities and workload to ensure proper planning and workforce mobilization to perform the activities. Train and coach on the validation and data integrity strategy and practices as well as practices related to CSV and data integrity.
    • neuchâtel, neuchâtel
    • temporary
    Randstad Professionals is looking for a Product Surveillance Scientist  for a major client in the tobacco industry based in Neuchâtel.Start Date: ASAPContract Duration: one yearYour tasks would be to manage assigned safety surveillance activities occurring in a post-market setting for all applicable reduced-risk-products. Leveraging well-established standards, methods and knowledge acquired in the highly regulated drug/medical device environment to the new area of tobacco product assessment requires great agility and excellent detail orientation while working in a dynamic environment.Your responsibilities:Ensuring the collection of all adverse event complaints throughout the different collection channels set-up and ensuring timely transfer to the case processing teamActing as a key player for any needed case clarification for case processing activities and managing follow-up requests by liaising with the marketMonitoring and tracking of cases requiring submission to local competent authorities and ensuring timely transfer to Regulatory Affairs departmentPerforming regular case monitoring for potential escalation of safety cases of concern to internal stakeholdersOrganizing and conducting safety trainings for successful implementation of post-market safety surveillance activitiesSupporting in routine data quality monitoring of safety data received from markets and implementing corrective actions as neededPerforming data analysis and producing results to communicate information as needed to internal stakeholdersKeeping working documents for operational activities up-to-date If you are interested to take on these responsibilities you should have the following requirements:Graduated with a BSc or MSc in Life SciencesUp to 2 years experience in a Safety/Pharmacovigilance (PV), Quality or Regulatory affairs roleExperience in developing/maintaining Safety processes is an assetGood knowledge in EU pharmacovigilance (GVP)Experience in working with Safety Database (e.g. Argus and/or Arisg) would be an advantageBasic training in coding with MedDRAIf you are willing to learn new things and interested in working in a regulated environment we are waiting for you. We are looking forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    Randstad Professionals is looking for a Product Surveillance Scientist  for a major client in the tobacco industry based in Neuchâtel.Start Date: ASAPContract Duration: one yearYour tasks would be to manage assigned safety surveillance activities occurring in a post-market setting for all applicable reduced-risk-products. Leveraging well-established standards, methods and knowledge acquired in the highly regulated drug/medical device environment to the new area of tobacco product assessment requires great agility and excellent detail orientation while working in a dynamic environment.Your responsibilities:Ensuring the collection of all adverse event complaints throughout the different collection channels set-up and ensuring timely transfer to the case processing teamActing as a key player for any needed case clarification for case processing activities and managing follow-up requests by liaising with the marketMonitoring and tracking of cases requiring submission to local competent authorities and ensuring timely transfer to Regulatory Affairs departmentPerforming regular case monitoring for potential escalation of safety cases of concern to internal stakeholdersOrganizing and conducting safety trainings for successful implementation of post-market safety surveillance activitiesSupporting in routine data quality monitoring of safety data received from markets and implementing corrective actions as neededPerforming data analysis and producing results to communicate information as needed to internal stakeholdersKeeping working documents for operational activities up-to-date If you are interested to take on these responsibilities you should have the following requirements:Graduated with a BSc or MSc in Life SciencesUp to 2 years experience in a Safety/Pharmacovigilance (PV), Quality or Regulatory affairs roleExperience in developing/maintaining Safety processes is an assetGood knowledge in EU pharmacovigilance (GVP)Experience in working with Safety Database (e.g. Argus and/or Arisg) would be an advantageBasic training in coding with MedDRAIf you are willing to learn new things and interested in working in a regulated environment we are waiting for you. We are looking forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    • neuchâtel, neuchâtel
    • temporary
    Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.The Process Excellence Engineer is responsible for implementing key business improvement initiatives for manufacturing lines. He/She defines opportunities, analyzes data, designs manufacturing line flows, and improves business processes. Improvement initiatives are led by enlisting and influencing cross-functional teams that deliver tangible business results through the application of Lean and Six Sigma principles, methodologies and tools. Utilizing business, leadership and technical skills, the Process Excellence Engineer will both execute projects and mentor all groups (associate to management) at the site, developing a continuous improvement culture.Main Responsibilities :Responsible for developing a strategy and executing a plan to deliver process performance improvements related to Quality, Delivery, and Cost of a manufacturing line or business unit within a plantManages project portfolio activities such as prioritization, resource allocation, performance measurement, and change management plansSupport the process for New Ideas pipeline, to deliver sustainable cost savingsDevelops strategy and execution plan to improve flow of products from suppliers to distribution centers for a value streamLeverages process knowledge to identify opportunities / solutions to improve throughput capacity by reducing impact of constraintsIs responsible for driving associates' engagement and for developing Lean and Six Sigma capabilities through coaching and mentoring at various level (associate to professionals) within the siteSustains business improvement results through the application of Lean, Six Sigma, JJPS business standards and other continuous improvement methodologiesFacilitates PEx trainings, certifications, business case definitions, and results presentations; as requiredFollows and observes all regulatory requirements (GMP's, ISO, FDA, internal policies, …) applicable to area of responsibilityComplies with J&J safety requirements and safe working conditions and practices in the departmentResponsible for communicating business related issues or opportunities to next management levelFor those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicableResponsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and proceduresPerforms other duties assigned as needed
    Caring for the world … one person at a time inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that is anchored in the internationally applicable Credo. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 134,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.The Process Excellence Engineer is responsible for implementing key business improvement initiatives for manufacturing lines. He/She defines opportunities, analyzes data, designs manufacturing line flows, and improves business processes. Improvement initiatives are led by enlisting and influencing cross-functional teams that deliver tangible business results through the application of Lean and Six Sigma principles, methodologies and tools. Utilizing business, leadership and technical skills, the Process Excellence Engineer will both execute projects and mentor all groups (associate to management) at the site, developing a continuous improvement culture.Main Responsibilities :Responsible for developing a strategy and executing a plan to deliver process performance improvements related to Quality, Delivery, and Cost of a manufacturing line or business unit within a plantManages project portfolio activities such as prioritization, resource allocation, performance measurement, and change management plansSupport the process for New Ideas pipeline, to deliver sustainable cost savingsDevelops strategy and execution plan to improve flow of products from suppliers to distribution centers for a value streamLeverages process knowledge to identify opportunities / solutions to improve throughput capacity by reducing impact of constraintsIs responsible for driving associates' engagement and for developing Lean and Six Sigma capabilities through coaching and mentoring at various level (associate to professionals) within the siteSustains business improvement results through the application of Lean, Six Sigma, JJPS business standards and other continuous improvement methodologiesFacilitates PEx trainings, certifications, business case definitions, and results presentations; as requiredFollows and observes all regulatory requirements (GMP's, ISO, FDA, internal policies, …) applicable to area of responsibilityComplies with J&J safety requirements and safe working conditions and practices in the departmentResponsible for communicating business related issues or opportunities to next management levelFor those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicableResponsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and proceduresPerforms other duties assigned as needed
    • neuchâtel, neuchâtel
    • temporary
    Randstad Professionals is looking for a Computational Biologist  for a major client in the tobacco industry based in Neuchâtel. Contract period: 4 monthsStart date: 01.09.2020 As a key part of a highly skilled multidisciplinary team that executes scientifically and technically challenging projects, you will bring your computational skills and your experience in network biology to the analysis and interpretation of a broad range of omics data. This requires that you interact closely with a wide range of experts, including computational biologists and experimental scientists. Your responsibilities:Support the development of biological network model relevant to our toxicological assessment studiesProcess gene expression datasets, perform  analyses, and support the biological interpretation of the resultsContribute to the integration of multi-modality systems biology dataDevelop computational tools and workflows that support these activities If you are interested to take on these responsibilities you should have the following requirements:PhD in computational biology, applied mathematics, computational toxicology, bioinformatics or a related fieldExperience in applying and developing network biology computational methodologiesExperience in processing Affymetrix  and RNAseq dataGood  statistical knowledge (estimation methodologies, experimental design)Proficiency in R programming, ShinyApp development is a plusBasic understanding of molecular biology mechanismsComputational data mining expertise and ability to interrogate, interpret, and visualize biological and toxicological dataFluency in both written and spoken English is a must. If you are good at leading a wide variety of studies and taking ownership, you enjoy learning while operating in an inquisitive and changing environment working collaboratively with cross-functional teams, you are excellent in delivering results in a timely manner and have an effective and impactful communication style, you are the one we want for this position as a Computational Biologist. We look forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    Randstad Professionals is looking for a Computational Biologist  for a major client in the tobacco industry based in Neuchâtel. Contract period: 4 monthsStart date: 01.09.2020 As a key part of a highly skilled multidisciplinary team that executes scientifically and technically challenging projects, you will bring your computational skills and your experience in network biology to the analysis and interpretation of a broad range of omics data. This requires that you interact closely with a wide range of experts, including computational biologists and experimental scientists. Your responsibilities:Support the development of biological network model relevant to our toxicological assessment studiesProcess gene expression datasets, perform  analyses, and support the biological interpretation of the resultsContribute to the integration of multi-modality systems biology dataDevelop computational tools and workflows that support these activities If you are interested to take on these responsibilities you should have the following requirements:PhD in computational biology, applied mathematics, computational toxicology, bioinformatics or a related fieldExperience in applying and developing network biology computational methodologiesExperience in processing Affymetrix  and RNAseq dataGood  statistical knowledge (estimation methodologies, experimental design)Proficiency in R programming, ShinyApp development is a plusBasic understanding of molecular biology mechanismsComputational data mining expertise and ability to interrogate, interpret, and visualize biological and toxicological dataFluency in both written and spoken English is a must. If you are good at leading a wide variety of studies and taking ownership, you enjoy learning while operating in an inquisitive and changing environment working collaboratively with cross-functional teams, you are excellent in delivering results in a timely manner and have an effective and impactful communication style, you are the one we want for this position as a Computational Biologist. We look forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    • neuchâtel, neuchâtel
    • temporary
    For our client Philip Morris SA in Neuchâtel, we are seeking an : Education & Training Pillar CoordinatorInitial entry date : as soon as possibleDuration : 6 months In this role you will have the following tasks:Support E&T pillar team to coordinate the master plan execution for capability building in MSMaintain the Fuse page for MS with available training to employees and provide necessary information about sessionsEnsure proper maintenance of training needs assessment and identify skills or knowledge gaps that need to be addressedAssess instructional effectiveness and determine the impact of training on employee skills and KPIs. Assess training effectivenessGather feedback from trainers and trainees following deployment of a specific skill learning interventionPartner with internal stakeholders and liaise with experts regarding instructional designMaintain Qualification Matrix and training records
    For our client Philip Morris SA in Neuchâtel, we are seeking an : Education & Training Pillar CoordinatorInitial entry date : as soon as possibleDuration : 6 months In this role you will have the following tasks:Support E&T pillar team to coordinate the master plan execution for capability building in MSMaintain the Fuse page for MS with available training to employees and provide necessary information about sessionsEnsure proper maintenance of training needs assessment and identify skills or knowledge gaps that need to be addressedAssess instructional effectiveness and determine the impact of training on employee skills and KPIs. Assess training effectivenessGather feedback from trainers and trainees following deployment of a specific skill learning interventionPartner with internal stakeholders and liaise with experts regarding instructional designMaintain Qualification Matrix and training records
    • neuchâtel, neuchâtel
    • temporary
    Pour notre client Philip Morris, nous sommes à la recherche d'un : Technicien de laboratoire6 mois renouvelable Le candidat rejoindra le département « Testing Laboratories » chez Philip Morris International. Le groupe se focalise non seulement sur la caractérisation des matériaux et substrats utilisés dans le contexte des Produits à Risque Réduit (RRP's) pour supporter les activités de prototypage du département « Product Development » mais aussi sur l'évaluation des produits de la compétition, etc. Responsabilités: Gestion des échantillons et communication avec les différents intervenants.Analyses chimiques principalement (GC-MS, headspace, GC-FID, viscosity, pH, KF, etc) mais aussi physiques selon les besoins (compression, titrations, etc.) d'une nature répétitive dans le but de générer des données de haute qualité.Assurer la « business continuity » en maintenant, calibrant et effectuant les réparations usuelles des équipements de laboratoire. Planifier les maintenances externes selon le planning. Assurer une quantité suffisante de fournitures de laboratoire.Assurer et monitorer les conditions environnementales du laboratoire lorsque requis.Supporter la mise en place et maintenir le système qualité en appliquant les procédures en vigueur au laboratoire.
    Pour notre client Philip Morris, nous sommes à la recherche d'un : Technicien de laboratoire6 mois renouvelable Le candidat rejoindra le département « Testing Laboratories » chez Philip Morris International. Le groupe se focalise non seulement sur la caractérisation des matériaux et substrats utilisés dans le contexte des Produits à Risque Réduit (RRP's) pour supporter les activités de prototypage du département « Product Development » mais aussi sur l'évaluation des produits de la compétition, etc. Responsabilités: Gestion des échantillons et communication avec les différents intervenants.Analyses chimiques principalement (GC-MS, headspace, GC-FID, viscosity, pH, KF, etc) mais aussi physiques selon les besoins (compression, titrations, etc.) d'une nature répétitive dans le but de générer des données de haute qualité.Assurer la « business continuity » en maintenant, calibrant et effectuant les réparations usuelles des équipements de laboratoire. Planifier les maintenances externes selon le planning. Assurer une quantité suffisante de fournitures de laboratoire.Assurer et monitorer les conditions environnementales du laboratoire lorsque requis.Supporter la mise en place et maintenir le système qualité en appliquant les procédures en vigueur au laboratoire.
    • neuchâtel, neuchâtel
    • temporary
    Randstad Professionals is looking for a Clinical Study Administrator for a major client in the tobacco industry based in Neuchâtel. Your tasks would be: Management of the Study Master File and support to Study Managers during conduct of assessment studies including set-up, maintenance of paper and/or electronic SMF Regular quality control of the SMFs to verify completeness and to check that CROs/sites and external vendors file documents as per agreed SMF structureProvide support in follow-up of invoices related to assessment studies conduct including the quality control of invoices against contracts as per work instructions and in agreement with Study Managers approve and file all invoicesSupport to Study Teams including co-ordination of reviews of SMFs by all functions involved in study conduct If you are interested to take on these responsibilities you should have the following requirements:1-2 yrs experience with Electronic Document Management System and/or electronic Study Master Files from pharma industry Experience in clinical studiesGood knowledge of MS Office Suite, capacity to learn the use of other IT toolsGood knowledge of Good Clinical Practice (GCP)Fluent English, knowledge of other languages is an advantage. If you are willing to learn new things and interested in new technologies we are waiting for you. We are looking forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    Randstad Professionals is looking for a Clinical Study Administrator for a major client in the tobacco industry based in Neuchâtel. Your tasks would be: Management of the Study Master File and support to Study Managers during conduct of assessment studies including set-up, maintenance of paper and/or electronic SMF Regular quality control of the SMFs to verify completeness and to check that CROs/sites and external vendors file documents as per agreed SMF structureProvide support in follow-up of invoices related to assessment studies conduct including the quality control of invoices against contracts as per work instructions and in agreement with Study Managers approve and file all invoicesSupport to Study Teams including co-ordination of reviews of SMFs by all functions involved in study conduct If you are interested to take on these responsibilities you should have the following requirements:1-2 yrs experience with Electronic Document Management System and/or electronic Study Master Files from pharma industry Experience in clinical studiesGood knowledge of MS Office Suite, capacity to learn the use of other IT toolsGood knowledge of Good Clinical Practice (GCP)Fluent English, knowledge of other languages is an advantage. If you are willing to learn new things and interested in new technologies we are waiting for you. We are looking forward to receiving your online application.Please note a Swiss Work permit or EU-citizenship is mandatory for this position.
    • neuchâtel, neuchâtel
    • temporary
    For our client Philip Morris SA in Neuchâtel, we are seeking an :Shift Leader EngineerInitial entry date : as soon as possibleDuration : Open endedSupervise and leads laboratory technicians in order to generate and provide scientific data to sustain the development of Reduce Risk product (RRPs) prototypes. You will be responsible for supervising, managing and motivating team members on a daily basis. Ensure the best laboratory practices are followed. Ensure safety and full compliance with policies and other relevant regulations in the laboratories.Responsibilities:Perform allocating resources to provide and maintain the capacity of the Lab. Set clear objectives and measure results (SMART goal setting) for direct reportsOversee day-to-day operation Monitor team performance and report on metricsMaintain Good understanding of different projects and partner's needs and maintaining a high level of RRPs business Identify any potential deviation and take corrective measures including appropriate reporting of such actions Collect Discover training needs and provide coaching Listen to team members' feedback and resolve any issues or conflicts Create an inspiring team environment with an open communication cultureRecognize high performance and reward accomplishments, encourage creativity and risk-taking
    For our client Philip Morris SA in Neuchâtel, we are seeking an :Shift Leader EngineerInitial entry date : as soon as possibleDuration : Open endedSupervise and leads laboratory technicians in order to generate and provide scientific data to sustain the development of Reduce Risk product (RRPs) prototypes. You will be responsible for supervising, managing and motivating team members on a daily basis. Ensure the best laboratory practices are followed. Ensure safety and full compliance with policies and other relevant regulations in the laboratories.Responsibilities:Perform allocating resources to provide and maintain the capacity of the Lab. Set clear objectives and measure results (SMART goal setting) for direct reportsOversee day-to-day operation Monitor team performance and report on metricsMaintain Good understanding of different projects and partner's needs and maintaining a high level of RRPs business Identify any potential deviation and take corrective measures including appropriate reporting of such actions Collect Discover training needs and provide coaching Listen to team members' feedback and resolve any issues or conflicts Create an inspiring team environment with an open communication cultureRecognize high performance and reward accomplishments, encourage creativity and risk-taking
    • neuchâtel, neuchâtel
    • temporary
    For our client Philip Morris SA in Neuchâtel, we are seeking a Senior AnalystInitial entry date : as soon as possibleDuration : 6 monthsYou will join the Manufacturing Solutions (Engineering) department in Neuchatel, Switzerland, whose objectives are to develop solutions for solving chronical problems in our manufacturing technology, to industrialize new technologies for our portfolio of products, and to identify solutions for boosting our agility and ultimately to contribute to our objective of a step change in financial performance.You will be responsible for the financial and planning activities of Manufacturing Solutions department.Specifically, you will:Lead the preparation of Manufacturing Solutions department's budgets, ensure that they are analyzed, commented and presented in accordance with management requirements.Establish a routine process within Manufacturing Solutions departments for the original budgets (OB's) preparation and revised forecasts (RF's), covering Capex, Project Expenses and departmental expenditures.Periodically monitor the department's expenditures, control and adjust them in agreement with management.Plan and control Capex and Project Expenses for all Manufacturing Solutions projects.Prepare capital investment requests (650's) and high quality justifications / explanations (Business Case) for Manufacturing Solutions projects. Prepare and monitor relative cash flows in collaboration with project managers / leaders.Prepare ad-hoc financial estimates, analyses and reports.Be responsible and monitor all departments' goods and services purchases. Propose improvements of the reporting systems, methods of work and analysis and contribute to ensuring that they are continuously adapted to the business requirements.Support Projects Portfolio & Planning management related to other Engineering / Planning activities such as management presentations preparation, support to Project Management Office (PMO), inventory control of PMIE assets, etc.
    For our client Philip Morris SA in Neuchâtel, we are seeking a Senior AnalystInitial entry date : as soon as possibleDuration : 6 monthsYou will join the Manufacturing Solutions (Engineering) department in Neuchatel, Switzerland, whose objectives are to develop solutions for solving chronical problems in our manufacturing technology, to industrialize new technologies for our portfolio of products, and to identify solutions for boosting our agility and ultimately to contribute to our objective of a step change in financial performance.You will be responsible for the financial and planning activities of Manufacturing Solutions department.Specifically, you will:Lead the preparation of Manufacturing Solutions department's budgets, ensure that they are analyzed, commented and presented in accordance with management requirements.Establish a routine process within Manufacturing Solutions departments for the original budgets (OB's) preparation and revised forecasts (RF's), covering Capex, Project Expenses and departmental expenditures.Periodically monitor the department's expenditures, control and adjust them in agreement with management.Plan and control Capex and Project Expenses for all Manufacturing Solutions projects.Prepare capital investment requests (650's) and high quality justifications / explanations (Business Case) for Manufacturing Solutions projects. Prepare and monitor relative cash flows in collaboration with project managers / leaders.Prepare ad-hoc financial estimates, analyses and reports.Be responsible and monitor all departments' goods and services purchases. Propose improvements of the reporting systems, methods of work and analysis and contribute to ensuring that they are continuously adapted to the business requirements.Support Projects Portfolio & Planning management related to other Engineering / Planning activities such as management presentations preparation, support to Project Management Office (PMO), inventory control of PMIE assets, etc.
    • neuchâtel, neuchâtel
    • permanent
    Our client is a national company based in Neuchâtel. This is a great opportunity to live and work in one of the most interesting and financially stable cities in Switzerland. Randstad Professionals is actively looking for a Java Security Developer (French and German speaking) to join a dynamic and growing team. Your mission :- Within the IT team, you will develop secure applications in an Agile manner and with a wide choice of technologies around Java language. Your profile: - Good knowledge of Java languages- You have experience in application security and a strong motivation to work in this environment. You know the rules of the OWASP foundation as well as HP Fortify (Software security test) is a plus- Good knowledge in cryptography- Knowledge of the main frameworks (Spring, JPA, ...) 
    Our client is a national company based in Neuchâtel. This is a great opportunity to live and work in one of the most interesting and financially stable cities in Switzerland. Randstad Professionals is actively looking for a Java Security Developer (French and German speaking) to join a dynamic and growing team. Your mission :- Within the IT team, you will develop secure applications in an Agile manner and with a wide choice of technologies around Java language. Your profile: - Good knowledge of Java languages- You have experience in application security and a strong motivation to work in this environment. You know the rules of the OWASP foundation as well as HP Fortify (Software security test) is a plus- Good knowledge in cryptography- Knowledge of the main frameworks (Spring, JPA, ...) 
    • neuchâtel, neuchâtel
    • contract
    For an international tobacco company in Neuchâtel, we are looking for an: Senior Method Development Scientist (Chemical) Contract start date: immediatelyContract length: 6 monthsYou will be responsible for ensuring the delivery and quality of new and improved physical methods to test materials and, finished and semi-finished goods;  Responsibilities:  In collaboration with project teams, testing engineering, testing labs and CoE labs define and draft method development programs and project plans ensuring timelines, required resources and deliverables are aligned with relevant stakeholders. Ensures methods chosen are appropriate for end use and aligned to best practice. Deliver new and improved methods of the correct quality to agreed timelines. The role is expected to both deliver methods and supervise others to ensure delivery. As a subject matter expert in physical measurement sciences, the role holder is expected to supervise, train and mentor method development scientists and contractors to ensure the quality of delivered methods. Lead point of contact for Testing Labs and Centres of Excellence to advice, troubleshoot and improve methods deployed to the business.Use analytical expertise to review and renew the physical methods portfolio. Identify areas of the portfolio which no longer meet business needs or best practice and develop improvement plans. Contribute to cost benefit analysis of improvement plans. In collaboration with lab governance identify suitable external method development partners, identify appropriate opportunities and, initiate and manage external method development projects to ensure delivery on time and correct quality. Technical management of the method transfer from external suppliers to the customer laboratory. Skills and Competencies: Education College/University<>Degree in Mechanical or Materials Engineering or equivalent skills through demonstrated experience (PhD or Master level or equivalent). Ideally formal project management qualifications.Work Experience>10 years’ experience in physical measurement with a minimum 5 years’ experience in applying physical measurement sciences in an industrial setting, ideally in the tobacco, FMCG and/or pharmaceutical industries. Extensive knowledge of the Tobacco industry and RRP and their development, testing and characterisation is preferred. Knowledge and experience of analytical sciences in a certified environment, ISO17025 and/or cGxP. Experience of method development is required, with a preference experience in the analysis of RRP materials and products is preferred Experience managing people and specifically physical engineers. Experience in project management in an R&D setting.Functional Skills Excellent written and presentation skills. Fluent in English. Expertise in at least one and experience and/or knowledge of a broad techniques to evaluate physical properties including but not limited to strength, mechanical, electrical, magnetic, imaging, others Ability to balance short term delivery and long term development. Ability to delivery in a pressured and fluid environment. Evidence of supervision and mentoring scientist. Proven ability to develop and delivery programs and projects. Other Competencies Action oriented, Problem solving, Dealing with ambiguity, Innovation management, Informing, Business Acumen, Motivating and influencing others, Customer focus, Organizational agility.  Please note a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position 
    For an international tobacco company in Neuchâtel, we are looking for an: Senior Method Development Scientist (Chemical) Contract start date: immediatelyContract length: 6 monthsYou will be responsible for ensuring the delivery and quality of new and improved physical methods to test materials and, finished and semi-finished goods;  Responsibilities:  In collaboration with project teams, testing engineering, testing labs and CoE labs define and draft method development programs and project plans ensuring timelines, required resources and deliverables are aligned with relevant stakeholders. Ensures methods chosen are appropriate for end use and aligned to best practice. Deliver new and improved methods of the correct quality to agreed timelines. The role is expected to both deliver methods and supervise others to ensure delivery. As a subject matter expert in physical measurement sciences, the role holder is expected to supervise, train and mentor method development scientists and contractors to ensure the quality of delivered methods. Lead point of contact for Testing Labs and Centres of Excellence to advice, troubleshoot and improve methods deployed to the business.Use analytical expertise to review and renew the physical methods portfolio. Identify areas of the portfolio which no longer meet business needs or best practice and develop improvement plans. Contribute to cost benefit analysis of improvement plans. In collaboration with lab governance identify suitable external method development partners, identify appropriate opportunities and, initiate and manage external method development projects to ensure delivery on time and correct quality. Technical management of the method transfer from external suppliers to the customer laboratory. Skills and Competencies: Education College/University<>Degree in Mechanical or Materials Engineering or equivalent skills through demonstrated experience (PhD or Master level or equivalent). Ideally formal project management qualifications.Work Experience>10 years’ experience in physical measurement with a minimum 5 years’ experience in applying physical measurement sciences in an industrial setting, ideally in the tobacco, FMCG and/or pharmaceutical industries. Extensive knowledge of the Tobacco industry and R