Gehaltsübersicht für in Kanton Neuenburg

Pour une manufactue horlogère de renom située au Val-de-Travers, nous recherchons, pour un poste fixe, un (e) constructeur mouvementConstructeur mouvement (H/F) Votre mission Développement complet de mouvements, modules et complications mécaniques Responsabilité technique de tous vos projets Suivi des mises au point et homologation laboratoire jusqu'à la série 0 Validation des dossiers techniques et suivi de l'amélioration continue Recherche de nouvelles idées, force de propositions Veille technologique Votre profil Ingénieur/technicien en microtechnique (option conception horlogère) ou titre jugé équivalent Expérience significative dans le développement de mouvements horlogers Excellentes connaissances de la construction de mécanismes horlogers Bonnes connaissances de produits Autodesk (Inventor 2D/3D, Vault, etc.) Connaissances des outils de créativité (Design Thinking, Triz, etc.), un plus ! Très bon esprit d'équipe, aisance relationnelle et leadership Créatif, polyvalent et autonome Stéphane BerthoudPlace de la Gare 1 / 2114 Fleurier+41 32 860 15 15 Écrire un email

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary: The QC Specialist is part of the Sample Management Management & Incoming testing Packaging team in the Quality Control department at BMS Boudry. This team is responsible for the management of all QC samples, visual testing of samples, preliminary investigations on samples associated with product complaints as well as support activities for the QC department. The main responsibilities of the position will be to ensure the follow-up of laboratory samples (raw material, stability samples) from receipt to destruction, performed and review \"visual control\" laboratory tests, and provide logistical support to the logistical support to the Analytical QC group (e.g., stock management and ordering of consumables and laboratory equipment). QC analyst will also participate in projects relating to laboratory safety, new products, and continuous improvement. All activities will be performed in full compliance with laboratory procedures and safety rules (EHS) as well as Good Documentation and Good Manufacturing Practices (GDP and GMP). Duties/Responsibilities: Reception, reconciliation, destruction, referencing (...) of samples such as semi-finished products incoming raw materials, stability, standard, retention or special samples Perform the reception, testing, and raw data review for all primary and secondary packaging materials Execution and review of analyses such as AQL visual inspection of pharmaceutical products and of pharmaceutical products and referencing of semi-finished/finished products (...) Visual examination of Stability and Reference samples Preliminary investigation of complaint samples Management of Laboratory material orders (\"Kanban\" system, creation of order supplier contact, follow-up, reception and storage) Execution of actions (CAPA action, Change action, Deviation action...) associated with Quality Systems Participation in projects and implementation of continuous improvement actions in the laboratory Management of samples for external sites Participation and presentations at team meetings Team scheduling Drafting and updating procedures or work instructions Support during regulatory inspections Approval of Oracle Sampling Plan Master Data Management Launch and Variation Deviation opening Qualifications: Federal certificate in science or equivalent combination of education training and experience Minimum 5 years' experience in a GMP environment or in a regulated industry Good knowledge of quality control operations in a GMP-regulated environment Expertise of laboratory safety rules, general organization and workflows of a quality control laboratory Ability to perform, document and review simple tests following applicable procedures (use of simple equipment, visual inspections, etc… General computer literacy including MS Office. Good knowledge and ability to familiarize themselves quickly with new software and computerized systems Good knowledge of data integrity principles Effective verbal communication skills. Ability to interact with different levels of the organization: peers, team members, supervisor and other departments Good technical writing skills, experience writing GMP documents (procedures, and protocols) as well as deviations (be able to open a deviation) Fluent in French, professional command of English, written and verbal (B2) Strong organizational skills: ability to set and focus on priorities Capable of independent problem-solving Ability to work collaboratively and cross-functionally in project teams Ability to train peers; willingness to share knowledge and expertise Strong attention to details Flexible, able to adapt to change If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

Quelle est ma fonction ?A ce poste à responsabilités vous exécutez des opérations manuellement ou sur robot de protection d'usinage, de vernissage sur différentes matières selon les demandes. Ensuite vous contrôlez les résultats finaux, vous réalisez des tests dans le but d'améliorer et annoncez les différentes anomaliesDe quoi ai-je besoin pour réussir ?Vous êtes polyvalent sur différentes opérations, vous avez le goût des finitions, vous savez vous vous adaptez à l'évolution des produits et techniques ce métier est donc parfaitement fait pour vous. De Formation de base peintre en carrosserie, vous avez de l’expérience dans le vernissage horlogerie exigée et aisance dans la manipulation des produits chimiques.Qu'est-ce qui fait l'entreprise ?Appartenant à un grand groupe international, cette entreprise est spécialisée dans la fabrication de cadrans, la décoration de surfacesLanguesFrançais: C2 – MaîtriseLieu de travailLa Chaux de fonds N° de poste vacantBYM-9K2

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary In this role you will share oversight of Quality Control (QC) activities related to Drug Product and Incoming Material to ensure compliance with internal policies, procedures, and regulatory requirements. This position will provide support for design, execution, troubleshooting and monitoring of QC process and testing activities pertaining to raw material (including sampling), stability, in-process, and bulk product. You will be responsible for cGMP compliance of the laboratory area and operations under your responsibility as well as for applying and ensuring staff complies with Environmental Health & Safety applicable procedures. Key Responsibilities Manage team and ensures cGMP compliance of the laboratory area and operations under responsibility. Create a positive and collaborative team environment and ensure that Bristol Myers Squibb standards are met. Manages performance and provides technical guidance, coaching and support to team members. Assigns training requirements and monitors training status of assigned team members. Create team plans to ensure resources are properly allocated and utilized effectively. Ensures all equipment used for GMP testing is in a qualified state. Authors, reviews, and approves complex GMP documentation such as laboratory procedures, work practices, plans, protocols, and reports. Support and sustains Lean Lab initiatives such as 5S, deviation reduction, Right First Time, and inspection readiness. Actively participates in inspections by Health Authorities. Report metrics to monitor schedule progress and help identify risk areas. Supports budget definition and adherence to budget target. Support purchase requisitions and purchase orders are managed as appropriate to ensure business needs are met in timely manner. Oversee QC incoming material, stability, in-process and bulk product testing activities. Collaborate cross-functionally and interdepartmental to define testing priorities, assign work to team members, and monitor progress against schedule. Ensure timely completion of stability samples in compliant with company procedures. Review and approve documentation as required by laboratory procedures. Perform final approval and disposition of QC results. Provide technical support to QC team members. Ensure compendial compliance of excipients (USP, Ph. Eur., JP and JPE as applicable) and evaluates any non-compendial supplier test methods against in-house methods and specifications. Defines incoming testing requirements of Incoming Materials, including specifications. Oversee sampling plan and testing regimes for all Incoming Materials. Provides oversight of testing contracted to external laboratories. Represents QC in cross-functional teams supporting New Product Introductions, Qualification and Risk Assessments. Support Deviations, Investigations and Change Control Management Ensures Deviations, CAPAs and Change controls are handled appropriately and in a timely manner. Initiates and/or implement changes in controlled documents. Own or lead investigations in collaboration with internal and external functions, as required. Approve laboratory investigations, checklists, and deviations as SME/Area Manager. Work with impacted QC area functions to define appropriate and effective corrective and preventive actions (CAPAs). Ensure timely and compliant closure of QC deviations/investigations and CAPAs according to Bristol Myers Squibb procedures. Promotes safe practices and behaviors. Report immediately incidents to Environmental Health and Safety (EHS) department, participate in investigations and identify measures to prevent similar accidents in the future. Ensures that staff (including short duration and temporary contracts) is properly informed on hazards and trained to act in consequence. Promotes safe practices and behaviors, assure that EHS requirements are implemented and respected. Demonstrate Bristol Myers Squibb values. Performs other tasks as assigned. If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

Ces tâches t‘attendentEn tant que conseiller de mode dans le magasin, tu assumes le rôle d'hôte et d'ambassadeur de notre marque. C’est important que le client se sente à l'aise et satisfait. Cela comprend les tâches suivantes: Service et conseil à la clientèleActivité de caisseAide à l'analyse générale de la boutiqueVisual merchandising et l’organisation des vitrinesEntretenir et gérer les produitsAssurer un espace de vente attrayantCe que tu apportesLa motivation et le plaisir en tant que vendeur sont au centre de nos priorités. Bien qu'une formation et l’expérience dans le commerce de détail soient un avantage, elles ne sont pas nécessaires. Nous serions heureux de voir les éléments suivants: Passion pour la modePersonnalité orientée vers le serviceSociabilitéHaute flexibilité et fiabilitéUn engagement personnel supérieur à la moyenneMaîtrise du français commercialNous t‘offrons les avantages suivantsFais partie de notre équipe et profite de possibilités de développement rapide et de conditions de travail équitables. Il s'agit notamment de : Formation sur les produits et les ventesResponsabilité précocePossibilités de développementDes conditions d'emploi modernesDes remises intéressantes pour les employésNouvelles tenues saisonnièresEnvironnement de travail jeune et dynamiqueTu es prête à relever un défi passionnant dans une entreprise de mode internationale? Alors postule dès maintenant à l'adresse suivante:https://careers.calzedoniagroup.com/fr-CH/carriere/dettaglio-annuncio?JobID=176880204(Seulement les candidatures en ligne seront prises en considération)

We are currently seeking a Senior Quality System engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.This is an open ended temporary contract.Please note this vacancy requires fluency in French. Your responsibilities:QMS:Participate to procedure creation and updateEnsures GMP, GDP rules are known, understood and respected in the siteEnsure Quality System support to all departmentsEscalates quality issues and makes sure that appropriate actions are in place to fix the issue in acompliant manner.Manages or participates to quality projects CAPA:Act as CAPA Process OwnerEnsure CAPAs are managed in compliance with internal procedures as well as applicable standardsFollow up CAPA process and ensure CAPA are handled and documented adequatelyEnsure Audit process support to all departments AUDIT:Participates and supports internal and third party audits / inspectionsPerform internal auditsEnsure internal Audit planning is implemented and follow upEnsure Audit process support to all departments QUALITY PLAN:Ensure QP are managed in compliance with internal procedures as well as applicable standardsParticipates and supports the QP processEnsure QP process is implemented and follow upKPI, QMREnsure KPI and QMR are handled in compliance with internal procedures as well as applicablestandardsParticipates and supports the KPI, QMR processEnsure QP process is implemented and follow up Your profile:A minimum of a Bachelor Degree is required, preferable in Engineering, a Life Science or a related technical discipline.Minimum Experience of 5 years working in a Medical Device manufacturing environment is preferred.Fluent in French and EnglishKnowledge of Medical device standards and regulations such as ISO13485, 93/42 EEC, EUMDR 2017/47, 21 CFR part 820Good communication, organizational, negotiation and interpersonal skillsGood analytical problem-solving skills.Use of Agile, Oracle, EtQ, TWDUse of Microsoft office toolsGood knowledge of statistical techniques Those lines sound interesting ? We are looking forward to receiving your application.

StellenbeschreibungGleichen Sie hier die Stellenbeschreibung mit Ihren Job-Präferenzen ab. Sie können die Job-Präferenzen jederzeit in Ihrem Profil verwalten.Anstellungsart100%Arbeitsort2300 La Chaux-de-Fonds, NEVotre mission ? Communiquer les orientations qualité aux équipes de production ? Former la production aux critères qualité ? Assurer la mise à disposition, la formation, l’application et le respect des procédures/instructions en production ? Statuer sur les demandes de dérogation ? Réaliser des audits de processus et de postes de travail selon les référentiels internes ? Synthétiser et présenter les résultats des audits et suggérer les axes d’amélioration ? Enregistrer et assurer la gestion des avis internes, décider des actions curatives en collaboration avec les responsables concernés ? Analyser et présenter les indicateurs qualité internes et suggérer les actions correctives prioritaires à mettre en place ? Participer au groupe de résolution de problème et d’amélioration des processus ? Gérer les réclamations liées à la sous-traitance ? Mettre à jour la documentation qualité Votre profil ? Technicien en micromécanique, horlogerie ou qualité? A l’aise avec les critères esthétiques? Outils informatiques bureautiques? Lecture de plans et cotation ISO? Connaissance de métrologie générale? Méthodes de résolution de problèmes ? Autonome, entreprenant et force de proposition? Esprit analytique, logique et structuré? Dynamique et flexible? Esprit d’équipe et bon relationnelErstellen Sie ein Indeed-Konto, bevor Sie zur Website des Unternehmens weitergeleitet werden.2300 La Chaux-de-Fonds, NE

Tenir la comptabilité en conformité avec les règles comptables et fiscales en vigueur.Supervision de la trésorerie.Supervision des bouclements.Établir et soumettre les déclarations fiscales dans les délais impartis.Gérer les immobilisations et suivre les investissements de l'entreprise.Établir les comptes statutaires en conformité avec les normes comptables.Préparer et faciliter les audits internes et externes.Mettre en place et assurer le suivi du contrôle interne financier.Participer activement aux projets d'amélioration continue de la performance financière de l'entreprise.Formation supérieure en comptabilitéBrevet fédéral de spécialiste en finance en comptabilité un plusExpérience managériale un atoutExpérience de 3 à 10 ans dans un poste similaireUne expérience dans le secteur de l'industrie un plusDe très bonnes connaissances de Ms Office (Word, Excel, Outlook, etc.)De nature dynamique, engagé/eFrançais courant à l'oral et à l'écrit

Investment Support OfficerThe position reports to the Group Head of Investment Support team in Neuchâtel. Other working relationships include all members of Group Operations, FO, Dealing and Treasury, Banking and various external business contacts (Financial institutions). OVERALL PURPOSE The individuals will be responsible for executing instructions and various administrative tasks around investment management in an accurate way and by respecting appropriate deadlines. PRINCIPAL ELEMENTS & ACCOUNTABILITIES - Dealing of Single Hedge Funds and Private Placements - Managing and executing instructions like corporate actions, proxy votes, conversions, capital calls and distributions - Inputs prices and revaluations of assets in the systems - Keeping line by line clients investment accounting up to date - Collating KYC, FATCA and compliance documentation for fund administrators and other third parties - Preparing SWIFT payment instructions - Inputting investment transactions and maintaining & updating records in our in house integrated database systems - Reconciliation of data QUALIFICATIONS AND EXPERIENCE - Diplôme de l’Ecole de Commerce, CFC d’employé de commerce or equivalent. - HEG – a real plus - Min 2 years’ experience in a Financial environment SKILLS - English level equivalent to B2 - Good knowledge of MS office - Knowledge and understanding of Double Entry Bookkeeping and Multi-Currency accounting - Knowledge and understanding of Financial Products - Understand basic information re Trust and Company and the relationship between Trust and Company, Trustee and Beneficiaries. COMPETENCIES AND BEHAVIOURS - Communication Skills: Communicate openly, clearly and concisely - Teamwork: Support & work towards team goals - Teamwork: Share information, is helpful & co-operative - Planning and Organizing: Manage time effectively, is able to prioritize - Planning and Organizing: Schedule & manage workload effectively Rue du Puits-Godet 12 2000 Neuchâtel

Votre profil: Vous êtes titulaire d’un diplôme de Polymécanicien ou formation jugée équivalente ainsi qu’une formation TQ1/TQ2Vous pouvez justifier d’une expérience similaire concluanteVous avez d’excellente connaissances de l’usinage ainsi que de bonnes connaissances des équipements de mesureBonnes connaissances informatiques (MS Office, SAP)Vous êtes reconnu pour votre esprit d’analyse et de synthèseBon esprit d’équipe et très bon sens de la communication Vos tâches: Vous serez responsable de la programmation des équipements de mesureVous serez en charge des programmes de contrôle des en-cours ainsi que du contrôle finalVous devrez garantir les systèmes de mesure au travers d’analyses statistiques appropriéesVous effectuerez le contrôle qualité final (dimensionnel et esthétique) et devrez créer les gammes de contrôle, confirmer les opérations et saisir les résultats.Vous réaliserez les rapports de mesure et communiquerez aux fournisseursVous devrez rédiger les instructions Contrôle Qualité et tenir à jour le tableau du suivi de contrôleVous participerez à divers projets d’amélioration continueVous travaillerez en étroite collaboration avec le secteur mécanique