Gehaltsübersicht für Engineering in Neuchâtel

Expleo Life Sciences Switzerland assist the industry in the realization of their projects through engineering services and project management, safety and security, compliance and performance and through a specific offer \"digital transformation\". We are looking for a : Commissioning & Qualification (C&Q) Lead As part of the creation of a new dry form building, the C&Q Lead has the overall management responsibility of the C&Q Firm who will be responsible for Design Qualification, Factory Acceptance Tests, Site Acceptance Tests, Commissioning, Qualification, Hand Over, and Close Out. Key Responsibilities The C&Q Lead will provide oversight of the site commissioning and qualification organization in support of capital projects. The incumbent in this role will lead and manage an experienced team of colleagues and contractors focused on commissioning and qualifying facilities, utilities, dry forms process equipment and Computerized System The individual oversees C&Q work activities of major complexity to ensure on time and within budget completion. Responsible for driving the commissioning and qualification activities of a new facility (incl. Utilities, equipment, CSV, ...) according to standards and regulatory requirements. Lead a team of colleagues and contractors to achieve C&Q objectives aligned with capital project milestones and site goals. Approval the C&Q Firm deliverables. Effectively manages assigned resources to address priorities, meet schedules, maximize productivity, reduce costs, and increase efficiencies. Interface with multiple sites and departments (Engineering, Technical Services, MS&T, end user groups, QA, suppliers, Architectural / Engineering Contractor, Construction Management contractor, Asset Care Management contractor, and C&Q contractor) to accomplish predefined goals and to provide technical guidance including but not limited to facilities, utilities, building equipment, production dry forms equipment, automation, cleaning approach and Computerized System validation. Design and author the validation/qualification approach (plan), provide the scientific rationale and acceptance criteria, generate and review/approve commissioning, validation/qualification protocols/reports. Conduct, and assist others, in industry and regulatory research including research into industry standards/FDA guidelines for validation equipment / processes and make determinations regarding acceptance criteria and testing. Lead/support the project team, coordinate the execution of C&Q of the project, prepare project schedules and provide presentations to senior management / stakeholders on project status. Lead/support the completion of complex investigations, initiate change controls (incl. assessing impact of the change) and managing corrective action plans associated with C&Q activities Lead/Support the implementation of structures, tools, and processes to actively manage C&Q activities. Participate when required during internal and external audits forwhich they are a SME, by answering questions, reviewing qualifications and validations with auditors, and providing documentation Qualifications & Experience Minimum of 10 years of relevant pharmaceutical industry experience (with a focus on dry forms pharmaceutical application validation in a GMP environment). Minimum 10 years ‘experience in managing personnel and/or complex projects, including direct experience in managing different Commissioning/Qualification/Validation contractors and activities for large and complex projects. Strong problem-solving skills, strong verbal and written communication skills. Ability to work independently and to influence and work across organizational boundaries. Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required. Excellent command of English and preferably French language. Project and change management experience. Experience with Product Life Cycle Management. Experienced in Health Authority inspections (preparation, process, presentations, responses drafting, etc.) with direct interactions including face to face interaction and response to audit questions. The successful C&Q Lead candidate should have around 10+ years of industry experience, with project experience including green and/or brownfield projects in the pharmaceutical dry forms industry. In general, the selected C&Q Lead will be directly collaborating with the rest of the project core team, project controls, and site validation teams to direct the implementation of the project. Experience with the similar project management process, documents, and deliverables is advantageous. While the capital project manager will remain responsible for seeking funding approvals within the team and overseeing the success of the project, the C&Q Lead will be responsible for executing required steps within the Stage Gate project management process and ensuring successful collaboration with the rest of the project team. Additionally, the C&Q Lead will be the key driver in developing and updating the C&Q project budget/estimate and schedule, especially in the design phase and into the construction and C&Q phases. Our positions are accessible to people with disabilities Neuchâ2000 Neuchâtel

In Vitro Diagnostics ScientistWe are seeking an In Vitro Diagnostics Scientist to develop surface immunoassays and be a core member of our engineering team. The candidate will join a multi-disciplinary team dedicated to developing high-quality products. The ideal candidate is a team player, likes overcoming difficult challenges, enjoys learning new skills, and has a “hands-on” problem solving approach. This is an outstanding opportunity for a self-motivated individual to make a key contribution and increase their responsibilities in a high-growth start-up environment. Job responsibilities: As part of the 1DROP team, the candidate will develop diagnostic assays on the biosensor platform and will be expected to perform the following:• Take ownership of the development, optimization and commercialization of a range of diagnostic assays.• Functionalize diagnostic chips using surface modifications, deposition of capture reagents, detection reagents, and analytes, passivation from non-specific binding.• Characterize the developed assays using blood and serum samples and statistical analysis (sensitivity, specificity, accuracy).• Assist in writing technical requirements, design specifications, verification test plans and reports, and risk management plans. Our ideal candidate: • Bachelor, Master or PhD degree in biomedical engineering, biomaterials, molecular biology, biochemistry, life sciences or related field.• Experience integrating biological reagents (proteins, nucleic acids) with medical devices• Experience developing IVD assays and developing medical devices.• Understand the requirements for manufacturable devices and associated processes.• Demonstrated record of achievement and professional maturity in a corporate environment.• Excellent planning and problem solving skills.• Ability to balance multiple assignments simultaneously.• Effective communication skills and ability to communicate with all levels of the organization. Nice to have skills and experience: • Product development experience using and working with many of the following: microfluidics, molecular biology techniques including, biophotometer, fluorescence microscopy, protein and DNA microarrays.• Optimization and characterization of surface chemistry for biological systems.• Experience depositing proteins on surfaces using microarray spotters such as Arrayit, Bio-Rad, Agilent, Sonoplot.• Biological inkjet printers such as MicroDrop, GeSiM, Scienion.• Statistical analysis tools such as R, Julia, Python.• Experience working with a quality system in a regulated industry, preferably medical diagnostics or medical devices.

Biochip Platform DeveloperWe are seeking a Biochip Platform Developer to participate in the overall development, implementation, maintenance and extension of 1DROP’s microfluidics platform. The candidate will join a multi-disciplinary team dedicated to developing high-quality products. The ideal candidate is a team player, likes overcoming difficult challenges, enjoys learning new skills, and has a “hands-on” problem solving approach. This is an outstanding opportunity for a self-motivated individual to make a key contribution and increase their responsibilities in a high-growth start-up environment. Job responsibilities: • Investigating and solving the current challenges related to the industrialization of the microfluidics platform• Planning and analysing scenarios to characterize and improve the performance of 1DROP’s microfluidics platform, taking into account current constrains• Organizing timelines and taking responsibility for the platform development according to milestones and deadlines• Synchronizing with reader development and assay development to optimize manufacturability and to minimize design transfer time• Communicating results and progress to 1DROP’s team• Ensuring the rigorous implementation of the processes as per established procedures (SOPs) defined in the Quality Management System (QMS)• Contributing to the Technical Documentation with specifications, protocols, test scenarios and project reports, etc. and building up a Design History documenting all phases of the biochip platform development.• Following the market, the industry and 1DROP’s competitors, to investigate and evaluate novel or alternative technologies with potential benefits for the microfluidics platform, maximising product value and in alignment with 1DROP’s product and business strategy• Implementing laboratory best practices and ensuring compliance to the applicable General Safety and Performance Requirements (GSPR) list according to the In Vitro Diagnostic Medical Device Regulation (IVDR) with focus on microfluidics platform• Interacting, assisting and advising purchasing decisions Required competences for the position: • Master’s or PhD degree in mechanical, chemical or biomedical engineering or similar field, preferably with a focus towards microfluidics technologies for biosensing• 5+ years success record in microfluidics platform development, preferably in the medical technology industry• Advanced understanding of production requirements for device manufacturability and associated processes• Excellent project management skills and experienced in reporting on key microfluidics platform metrics• Strong ability to transfer microfluidic concepts with differentiated advantages over on-market competitor products into a viable product• Demonstrated in-depth knowledge working with many analytical & diagnostic instrumentations such as microfluidics, fluorescence imaging systems, photo-spectrometer and processes such as homogenous assay engineering or surface coating• Knowledge and experience working in a biochemistry laboratory with hazardous chemicals and biological samples• Ability to act decisively with strong negotiation skills to obtain materials within budget and on schedule and solve staff or equipment-related issues• Experienced in microfluidic design using AutoCAD, Solidworks, Rhino, or similar• Knowledge with image processing, statistical analysis and experimental planning, such as design of experiment, process design, characterization, and optimization and associated tools such as ImageJ, R, Python• Ability to work in a regulated environment with design control and compliance to ISO 13485, FDA cGMP, IVDR 2017/746• Independent and self–driven to improve processes and achieve targets• Analytical and structured workflow with attention to detail to ensure high levels of quality• Excellent English written and verbal communication and presentation skills and ability to communicate with all levels of the organization• Highly creative and inventive problem solver with a ‘hands-on’ personality and a can-do attitude• Calm under pressure, can thrive in a high-volume, continuously changing, fast-paced environment• Demonstrating flexibility and openness to execute tasks beyond the job description

Votre avenir est notre job ! L'entreprise HANS LEUTENEGGER SA est une entreprise suisse leader depuis 1965 dans l'industrie, l'ingénierie et la construction. En qualité de spécialistes de l'engineering, montage, travaux en régie et travail temporaire, nous profitons de la confiance d'une clientèle de première classe au niveau national et international. Afin de soutenir notre client, nous sommes à la recherche d'un Polymécanicien Polymécanicien monteur Vos responsabilités Montage de nouvelles machines Travaux d’usinage Mise en train des machines Etre garant de la qualité des produits finis Participer aux démarches d’améliorations continues Nous offrons Un environnement de travail et des conditions d'engagements motivants. La possibilité de rejoindre une société innovante et tournée vers le futur. Entrée De suite ou à convenir Votre profil CFC mécanique Maitrise des méthodes d’usinage Horaire à convenir Personne autonome et rigoureuse Hans Leutenegger SAFiliale NeuenburgAv. du 1er Mars 20,Case postale 2633CH-2001 Neuchâtel&+41 32 723 77 44

Software Integration EngineerAktiia was founded out of a passion to create the best solution for the diagnosis and management of hypertension. We are a venture-backed startup that recently closed a new financing round. Our technology is based on (15+) years of research by our founders at the prestigious Swiss research institution, CSEM. Aktiia's solution has been validated through extensive trials in acute and low-acute settings, with its accuracy receiving worldwide acknowledgment from medical and scientific experts. The Aktiia team (45 employees) is smart and driven, with colleagues who are all focused on bringing to market an innovative and impactful solution. To strengthen our team, we are looking for a: SOFTWARE INTEGRATION ENGINEER To lead the industrialization process of Aktiia Blood Pressure algorithms Responsibilities Lead the definition, implementation, testing and maintenance of interfaces between Aktiia Blood Pressure algorithms and different services running on our cloud servers. Maintain and improve the existing pipeline for deployment of Aktiia Blood Pressure algorithms into the cloud-based backend (C, Matlab). Design, implement and test new pipelines for deployment of new-generation Aktiia Blood Pressure algorithms into the cloud-based backend (Python). Work closely with the algorithm R&D team on the generation and maintenance of test scenarios and test cases for the Aktiia Blood Pressure algorithms. Act as the bridge between the R&D and Backend teams, ensuring smooth technical integration. Take the lead on documentation of all deployment and V&V related activities. Your profile BSc, MSc in computer science, electrical engineering or equivalent Excellent programming skills in C Significant experience in Matlab and Python Signal processing background is a plus 3+ years of experience in regulated environment is a major plus Strong analytical skills Proficient communication skills in English (written and spoken) Detail oriented Creative and hands-on approach to problem-solving Motivated, proactive, curious, enthusiastic, team player, structured, solution oriented and willing to learn Willingness to work with a multidisciplinary, multicultural and diversity-oriented team Swiss-located Are you passionate in solving problems with visionaries and innovative approaches? In this case you are ready to rock with Aktiia team. We look forward to receiving your application by email ([email protected]). Only fully documented applications (CV, motivation letter, diplomas, transcripts) will be considered for the recruitment process. If you should not hear back from us within two weeks, your application has unfortunately not been successful for this role.

Notre client, une société industrielle leader dans son domaine d’expertise, nous a mandatés afin de lui présélectionner son/sa futur/e Ingénieur R&D / Process (H/F) Dont la mission principale sera de réaliser l’analyse des procédés critiques (process à haut niveau de risque technique ou critique pour le produit du client) et concevoir des solutions pour le développement, le suivi du montage, la mise au point et la validation de ces procédés en s’appuyant sur les autres départements de l’engineering. Vos principales responsabilités consisteront à : • Pour les process critiques, définir les concepts mécatroniques et dimensionner théoriquement les éléments en accord avec les différents départements. Organiser et suivre les activités du process sur un ou plusieurs projets client. S’assurer que les activités et délivrables process sont planifiés de manière adéquate dans le planning projet. • Rédiger les protocoles et rapports de tests, exécuter ou organiser leur exécution. Réaliser la calibration des process critiques : design, procédures, exécutions et rapports. • Proposer et rédiger les offres process pour répondre aux besoins du client. Participer au chiffrage des heures nécessaires au process pour la réalisation du projet puis présenter au client les concepts de base du process et s’accorder avec lui sur la stratégie de contrôle. • Acquérir des connaissances des nouveaux process stratégiques. Suivre l’évolution technologique du marché et faire évoluer les choix techniques liés au process. Développer et utiliser les simulations numériques pour prédire et optimiser les process. Votre profil : • Master en ingénierie électronique/ électrotechnique/ mécanique /science des matériaux /physique ou informatique industrielle. • Au minimum une expérience au préalable dans la conception et le développement de procédés de fabrication. • Solides connaissances techniques pluridisciplinaires. Bonnes compétences organisationnelles. Capacité à planifier, coordonner et suivre plusieurs projets en parallèle ainsi que des sous-projets de manière autonome. • Excellentes compétences en communication afin de participer aux discussions techniques avec les clients et de pouvoir rédiger des présentations et des rapports, le plus souvent en anglais. • Très bonnes connaissances en anglais (minimum B2). Intéressé/e ? Alors n'hésitez pas à faire parvenir votre dossier complet accompagné de vos certificats et diplômes à Donato Dufaux qui le traitera en toute confidentialité. Seules les candidatures correspondant aux critères requis seront traitées ! 2000 Neuchâtel

Votre avenir est notre job ! L'entreprise HANS LEUTENEGGER SA est une entreprise suisse leader depuis 1965 dans l'industrie, l'ingénierie et la construction. En qualité de spécialistes de l'engineering, montage, travaux en régie et travail temporaire, nous profitons de la confiance d'une clientèle de première classe au niveau national et international. Notre client, une PME située dans canton de Neuchâtel, est à la recherche d'un Monteur en chauffage / Soudeur TIG Monteur en chauffage / Soudeur TIG Vos responsabilités Installation de chauffage, pompes à chaleur Lecture de plan Soudure TIG Maîtrise des procédés de sertissage pour tuyaux Nous offrons Un environnement de travail et des conditions d'engagements motivants. La possibilité de rejoindre une société innovante et tournée vers le futur. Entrée A convenir Votre profil Formation dans le domaine du chauffage Maîtrise de la soudure TIG exigée. Plusieurs années d'expériences en Suisse dans le domaine du chauffage Permis de conduire et véhicule Hans Leutenegger SAFiliale NeuenburgAv. du 1er Mars 20,Case postale 2633CH-2001 Neuchâtel&+41 32 723 77 44

Senior Process Engineer Jobdescription Senior Process Engineer Location: Canton of Neuchatel Type of contract: temporary,open-ended If you'd like to work in a dynamic and friendly environment in the medical devices field then this position is made for you ! This position requires fluency in both French and English. Your responsibilities: Activity linked to Manufacturing Engineering / Project Management Organize work in a common approach to projects. Ability to define objectives. Decisions on technical decisions on projects. Ensure project management with the project team at the technical level / deadlines /delivery / quality / regulatory compliance / safety / environment. Ensures the delivery of savings according to the project schedule. Capital request management (Capex). Ensures project pipeline availability. Process development or improvement: Analysis of current process / needs / definition of the environment to be respected / justification of profitability / supplier management / internal project management / participation in FMEA development / validation. Coordinates discussions and interventions with external providers and suppliers. Responsibility for process validations: Develop validation strategy, VAF (Validation Assessment Form), VP (Validation Plan) Equipment Installation Validator (IQ) Technical leader for writing OQ/PQ validations Your profile: Education Engineering degree or equivalent Fluency in French and English, spoken and written At least 3-5 years' experience in a similar field and function Technical skills Project Management Team Management Industrial technical knowledge Process / Physics knowledge Quality / Safety / Environment knowledge Mastery of statistical tools (Minitab, etc.) Knowledge of microtechnology processes Computer skills (Office, Excel macro, etc.) Relational / organizational skills Able to work in a team and independently Project team management, leadership and team-building skills Ability to synthesize, rigor Presentation of results Participation and leading of meetings in French and English Report writing Ability to train operators and technicians Ability to interpret complex situations, problem-solving and decision making Knowledge of the medical field and regulatory affairs Lucie Nasshan

Role Summary: The Legal Counsel is responsible for providing appropriate and responsive legal support and advice to the Company globally on a variety of legal matters, particularly in drafting, reviewing, and negotiating a broad range of contracts, domestic and international. This position must have a solid business orientation and focus on practical problem solving, while upholding the Company’s strong ethics, culture, and principles of integrity. Legal Counsel Duties & Responsibilities: Draft, review, and negotiate various types of agreements, from standard to complex, including commercial contracts, such as tenders, distribution, reseller and direct sales contracts, services agreements, vendors’ contracts and T&Cs, data privacy, and other agreements; Draft and maintain form sales contracts for all supported markets; Coordinate with and seek feedback and input from subject matter experts across Masimo to complete contract reviews and approvals; Identify legal risks and recommend and implement risk mitigation strategies: Support and advise Company on compliance matters, especially those relating to anti-corruption and data privacy; Provide responsive and effective legal support and guidance to all of Masimo’s business units as needed, including sales, marketing, supply chain, engineering, clinical research, and business development departments; Manage and direct outside counsel as necessary, including supervising their work and managing spend; Ensure compliance with U.S., EU and other international laws and regulations and Masimo policies and procedures; Support business initiatives and special projects, as assigned, including in areas of, intellectual property, compliance and competition law Minimum & Preferred Qualifications and Experience: Minimum Qualifications: Master’s degree in Law or equivalent as required to practice law in Europe or one of its countries; Three years of experience working in-house or a combination of in-house and reputable law firm: Significant experience drafting, reviewing, and negotiating a wide variety of contracts; Excellent analytical and creative problem-solving skills; Proficiency in English; Excellent written and verbal communication, research and presentation skills; Practical, logical, and efficient problem solve able to work cross-functionally; Strong work ethic, team player and positive attitude; Organized and keen attention to detail; Results oriented, self-motivated, and self-directed; Able to handle multiple concurrent assignments and assume personal responsibility for deliverables under tight deadlines, working well under pressure in a rapidly changing environment Preferred Qualifications: Knowledge of and experience with data protection and privacy laws, especially GDPR Experience working within a highly regulated industry such as medical device, biotechnology, or pharmaceuticals; Working knowledge of competition law Knowledge of and experience with laws and regulations applicable to medical technology companies, such as U.S. FCPA and UK Bribery Act, and other laws, regulations, and ethical codes that apply to medical device manufactures; Speak multiple languages, like German, Spanish and French (in addition to English); Experience managing and working with outside counsels. Route de Pierre-à-Bot 972000 Neuchâtel

Management des équipes - Piloter, suivre et coordonner l'équipe selon les objectifs définis - Gérer le développement des compétences - Assurer une communication ascendante et descendanteDéveloppement produit : de la faisabilité au lancement - En phase de faisabilité : proposer des solutions techniques, coordonner et valider les propositions - En phase de prototype : proposer une gamme de fabrication, superviser la fabrication du prototype - En phase de présérie/lancement : veiller au bon déroulement, identifier les modifications, assurer un support actifAmélioration continue - Travailler sur la performance de chaque poste de charge - Mettre en place le processus de résolution de problèmes - Proposer des solutions pour améliorer les processus existants - Capitaliser les propositions d'améliorationIntégration des nouveaux processus et investissements - Participer à la construction de la politique d'investissement - Être support lors de l'intégration de nouveaux équipements- Idéalement diplôme d'Ingénieur en microtechnique ou équivalent- Expérience de 3 ans minimum dans le secteur du luxe, idéalement dans l'habillage horloger - Bonne connaissance des techniques d'usinage, traitements de surface, et métallurgie- Connaissance de base des systèmes automatisés- Expérience managériale et leadership naturel- Sens de l'analyse, esprit d'initiative, et capacité à proposer des solutions pragmatiques- Personnalité dynamique, positive, rigoureuse, et orientée terrain- Capacité à communiquer de manière transverse et concise sur les projets et activités.