Gehaltsübersicht für Senior Project Leader in Schweiz

 Tasks & Responsibilities:• Builds, maintains and innovates processes and tools for Data Science portfolio management, resource allocation and project tracking• Supports setting the goals, ways if working and daily operations for the team• Guides DS portfolio management• Support scoping of projects and efficient resourcing• Leads development of DS prototypes in close collaboration with RIS Customer Areas, RIS chapters as well as external research and commercial partners• Plans, tracks and controls execution of the portfolio and the budget to ensure best allocation of resources• Prepares communication materials for multiple stakeholders• Facilitates the effective sharing of experiences and knowledge within Data Services and other relevant Data Science teamsMust haves:• Minimum a master in business / economics / computer science / biology / chemistry / engineering / computer science / medicine or epidemiology and/or MBA • Minimum 5 years of work experience in strategy consulting • Minimum 5 years experience in healthcare or life science environment • Minimum 5 - 7 years of top management consulting Nice to haves:• PhD• Experience with data privacy respective regulatory environment• Familiarity with regulatory framework and guidelines for pharmaceutical/diagnostics productsPersonal requirements:• Solves problems in a hypothesis-driven, structured, analytical, pragmatic and end-product focused approach• Thinks broadly, strategically, and timely when preventing, solving or managing problems, thinks quickly under pressure• Possesses excellent leadership, planning, organizational and analytic abilities, manages multiple tasks• Has the ability to identify and resolve critical issues and to assess the impact of decisions• Is an excellent listener and can spot new ideas, directions and potential conflicts in DS team early on• Actively establishes and maintains effective working relationships with other functions; is co-operative, takes cultural and value differences into account in dealings with others• Communicates flawlessly and effectively in written reports, presentations and meetings• Transparent leadership style ensuring that DS goals, its roles, and responsibilities are well communicated to the team members

12-Month ContractDay Rate: 1,250 CHFLocation: Zurich, SwitzerlandWorkplace: On-site (1 day WFH)Language(s): Fluent in German & English (Mandatory) **12-Month Contract, With the option to extend up to 5 years. The role will be part-time to start on September 23 moving to full-time from October 23 (100% Occupancy).**Are you a seasoned leader in program management and project leadership, with a passion for driving innovation in the automotive industry? Our client is seeking a dynamic Program Manager / Senior Project Leader to spearhead transformative initiatives. If you're ready to leverage your expertise and lead cross-functional teams toward success, we invite you to apply. The Role:As the Program Manager / Senior Project Leader, you'll play a pivotal role in driving and overseeing complex projects within the automotive domain. Your responsibilities will include:- Leading end-to-end program management, ensuring alignment with strategic goals and operational excellence.- Orchestrating cross-functional teams to deliver innovative solutions on time and within budget.- Collaborating closely with stakeholders to define project scope, objectives, and deliverables.- Monitoring project progress, identifying potential risks, and proactively implementing mitigation strategies.- Providing mentorship and guidance to team members, fostering a culture of collaboration and excellence.- Utilizing your exceptional communication skills to liaise with internal and external partners. Requirements:- 10+ years of progressive experience in program management and project leadership roles within the automotive industry.- Proven track record in successfully managing and delivering complex projects on time and within budget.- Fluent in both German and English, with excellent verbal and written communication skills.- Strong analytical mindset, capable of navigating challenges and driving data-informed decisions.- Exceptional leadership abilities, including the capacity to inspire and lead cross-functional teams.- A strategic vision, coupled with the ability to align projects with overarching business objectives.- Proficiency in leveraging project management methodologies to achieve results.- Passion for innovation and an unwavering commitment to driving continuous improvement.  Our client organizations are at the forefront of innovation within the automotive industry. As a Program Manager / Senior Project Leader, you'll have the opportunity to lead transformative initiatives that shape the future of the industry. Your expertise will drive meaningful change and contribute to their success. If you're a dynamic leader with a proven track record in program management and project leadership within the automotive sector, we encourage you to apply. Please submit your CV highlighting your relevant experience, leadership capabilities, and language proficiency. Join our clients in leading the charge in the automotive industry.  Über das Unternehmen:Rec2Tech Ltd

Senior Project Coordinator SAP Sep 19, 2023 2 min read Senior Project Coordinator SAP Updated: Jan 24 For our client a global pharmaceutical company we are looking for a SAP Senior Project Coordinator. The Company Our client is a global biopharmaceutical company located near Neuchatel, Switzerland Focused on R&D and delivery of innovative medicines across several therapeutic areas, including oncology, hematology, immunology, and CVD. The Role The objective is to implement or migrate from Oracle ERP to the new corporate SAP solution for the company's site in Switzerland. The position holder will oversee the ERP Integration Project (SAP), and support the Site Project Manager in planning and execution to deliver intended outcomes: Setup of site project management and governance structure in collaboration with IT Business Partners (ITBPs) and Global Digital Capability Managers (DCMs). Plan, track and deliver the targeted objectives of site & external manufacturing (ExM) project. Serve as a bridge between the Global Program Manager and Local site Project Management team for local activities. Build a schedule with the Program Manager and site stakeholders. Identify dependencies, evaluate risks/issues, and communicate status to appropriate levels of management and stakeholders across the project. Ensure site & ExM project deliverables, schedule, and financials adhere to established norms and are managed in alignment with best practices of GPS/GMO and IT GPS PMO. Support site & ExM project team to deliver according to the plan. Conduct or moderate site & ExM team (IT & Business) meetings and share minutes. Prepare project status reports and documentation to keep the Program Manager and Onsite project sponsors informed of project progress and potential risks/roadblocks so they can take appropriate action. Raise Project Change Request when scope, timelines, or budget change. Proactively remove obstacles to drive assigned projects’ momentum and progress. Engage and energize the project team and provide actionable insights to key stakeholders. Plan and recommend necessary resources to ensure successful completion of the assigned project. Advise and consistently apply Project Management best practices (including Agile, SDLC) and tools. Continuously improve our adoption and maturity of best practices across IT. Provide support to IT BPs and DCMs in the management of project financials, vendor management and procurement. You Our client is looking for someone who has: Computer science/Information Technology degree or equivalent. Minimum 5+ years’ experience as a Sr. Project Coordinator in Pharma, ERP Systems implementation – Preferably SAP and GxP Systems Implementation from requirements to delivery of final product and documentation included. Pharmaceutical, Biotechnology, Life Science industry experience. Experience in ERP Systems (Preferably SAP) implementation. Proficiency into System Development Lifecycle (SDLC) and Computer System Validation (CSV). Awareness of 21-CFR Part 11, Eudralex and other Regulatory compliance requirements. Familiar with Change Management processes and tools and regulated document authoring. Strong accountability in driving Project Coordination. Strong capability to facilitate Waterfall, Agile and Hybrid projects. Agile, flexible, autonomous in analysis, problem-solving and achieving deliverables. Service-oriented mindset. Business acumen. Strong relationship and collaboration skills (verbal and written) with IT and Business both Global and Onsite stakeholders. Constructive influencing of colleagues to a positive outcome. The below skills are a plus: PMP certification or equivalent. Business Analysis (BA) experience. ServiceNow PM module knowledge. Implementation of other standalone and interconnected computerized systems supporting Production activities. Only applicants eligible to work in Switzerland will be considered e.g. Swiss national, current Swiss work permit holder or cross-border EU citizen. ***We are no longer considering applications for this position, please contact [email protected] to be informed of future similar positions*** Consultants • Vacancies For our client a global pharmaceutical company we are looking for a SAP Senior Project Coordinator. The Company Our client is a global biopharmaceutical company located near Neuchatel, Switzerland Focused on R&D and delivery of innovative medicines across several therapeutic areas, including oncology, hematology, immunology, and CVD. The Role The objective is to implement or migrate from Oracle ERP to the new corporate SAP solution for the company's site in Switzerland. The position holder will oversee the ERP Integration Project (SAP), and support the Site Project Manager in planning and execution to deliver intended outcomes: Setup of site project management and governance structure in collaboration with IT Business Partners (ITBPs) and Global Digital Capability Managers (DCMs). Plan, track and deliver the targeted objectives of site & external manufacturing (ExM) project. Serve as a bridge between the Global Program Manager and Local site Project Management team for local activities. Build a schedule with the Program Manager and site stakeholders. Identify dependencies, evaluate risks/issues, and communicate status to appropriate levels of management and stakeholders across the project. Ensure site & ExM project deliverables, schedule, and financials adhere to established norms and are managed in alignment with best practices of GPS/GMO and IT GPS PMO. Support site & ExM project team to deliver according to the plan. Conduct or moderate site & ExM team (IT & Business) meetings and share minutes. Prepare project status reports and documentation to keep the Program Manager and Onsite project sponsors informed of project progress and potential risks/roadblocks so they can take appropriate action. Raise Project Change Request when scope, timelines, or budget change. Proactively remove obstacles to drive assigned projects’ momentum and progress. Engage and energize the project team and provide actionable insights to key stakeholders. Plan and recommend necessary resources to ensure successful completion of the assigned project. Advise and consistently apply Project Management best practices (including Agile, SDLC) and tools. Continuously improve our adoption and maturity of best practices across IT. Provide support to IT BPs and DCMs in the management of project financials, vendor management and procurement. You Our client is looking for someone who has: Computer science/Information Technology degree or equivalent. Minimum 5+ years’ experience as a Sr. Project Coordinator in Pharma, ERP Systems implementation – Preferably SAP and GxP Systems Implementation from requirements to delivery of final product and documentation included. Pharmaceutical, Biotechnology, Life Science industry experience. Experience in ERP Systems (Preferably SAP) implementation. Proficiency into System Development Lifecycle (SDLC) and Computer System Validation (CSV). Awareness of 21-CFR Part 11, Eudralex and other Regulatory compliance requirements. Familiar with Change Management processes and tools and regulated document authoring. Strong accountability in driving Project Coordination. Strong capability to facilitate Waterfall, Agile and Hybrid projects. Agile, flexible, autonomous in analysis, problem-solving and achieving deliverables. Service-oriented mindset. Business acumen. Strong relationship and collaboration skills (verbal and written) with IT and Business both Global and Onsite stakeholders. Constructive influencing of colleagues to a positive outcome. The below skills are a plus: PMP certification or equivalent. Business Analysis (BA) experience. ServiceNow PM module knowledge. Implementation of other standalone and interconnected computerized systems supporting Production activities. Only applicants eligible to work in Switzerland will be considered e.g. Swiss national, current Swiss work permit holder or cross-border EU citizen. ***We are no longer considering applications for this position, please contact [email protected] to be informed of future similar positions*** IT Senior Project Manager - Contract - Neuchatel Project Manager, Capital Engineering Global QA Patients Operations Manager - Japanese

Project Leader SAP PP & Supply ChainÜber unseren KundenFür unseren Kunden, der sich kontinuierlich weiterentwickelt und damit einen einzigartigen Mehrwert schafft, suchen wir:Ihr AufgabenbereichLead and contribution in conceptual system and process designResponsible for planning and worldwide implementation of the complex processes in the specific scope of the project (e.g. IBP – Integrated Business Planning)Customizing, implementation and rollout of global production and supply chain processesMonitoring of global business processes/workflows Documentation and TrainingActive support for digital transformation within production and the supply chain3rd level Support SAP Customer Competence Center (CCC)Close collaboration with global stakeholdersSupervising and coordination of external SAP consultantsIhr ProfilCertified computer scientist FH / HF or equivalent educationExpert Know How, experience and competence about opportunities and practical operation within specific processesKnowledge and Customizing in SAP PP / MM / QM / WM (SAP PI Process Industries, SAP Intercompany Processes, SAP PM, SAP S/4HANA)Project Management skillsFluent in German and EnglishPotential in leading a team, interdisciplinary, disciplinary and functionalConceptual thinker – strategic as well as pragmaticWilling to take responsibilityDeveloping of training concepts and execution of trainingsIhre ChanceFür unseren Kunden, der sich kontinuierlich weiterentwickelt und damit einen einzigartigen Mehrwert schafft, suchen wir:Ort:ZürichSpezialisierung: Sprachen: Job ID: 8704 |

Job Description: At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world. Every person at Ferring works together to change lives and help people build families. Our corporate teams offer empowering, innovative, challenging and rewarding careers – we are motivated to make a difference. To reach our full potential we collaborate, and respect and value diverse contributions so that we can grow as an organisation and as professionals. Together we can influence the world around us to make life and work better. Ferring+You As part of the Global Engineering Team, the Senior Project Engineering Manager will be responsible for planning, leading and managing the engineering, EHS, construction, commissioning and qualification of a new biotech facility project in close collaboration with other involved departments and stake holders (Site Head, Production, QA, Finance, legal, procurement, …) in a matrix organization. True leader with a strong technical experience and expertise in the pharma industry and mainly biotech, he/she will be the representative of Ferring Global Engineering for the day-to-day management of the projects, coordination with local Engineering Contractors, Control of the Budget & Schedule, reporting of the project health, monitoring the Engineering, Construction, Commissioning and Qualification Activities. The Senior Project Engineering Manager will report to Ferring Global Engineering for the Technical and financial parts of the Project. Your day at Ferring Lead projects from Engineering and Design through to Construction, Commissioning, and Qualification phases in collaboration with Local & Global Engineering, Contractors, and Ferring departments until Operational Qualification is achieved, including conducting after-action reviews. Provide Engineering Expertise and be the interface between Ferring Global Engineering, Program Lead, local Engineering / Maintenance, Contractors, and other Ferring departments according to the project organization set-up. EHS responsible for the duration of the project, provide technical support for the installation checks during the construction of the new facility, provide support for the commissioning and start-up of the new facility, provide qualification support for the new assets. Manage all contacts with local authorities for permitting, environmental, waste disposal, construction zone and facility cleaning etc. in close collaboration with the site organization. Oversee on-site execution activities in close collaboration with the site project team, site management, Global Project Management Office (PMO), and applying LEAN principles and construction tools. Coordinate activities with the site Engineering & Maintenance Department Support preparation of future maintenance plan, including calibration, and assist in the procurement and management of critical spare parts. Ensure effective coordination among all relevant Ferring departments, including MSAT, LQA & GQA, Legal, procurement, Production, LSC & GSC, as required. Coordinate the training of Engineering & Maintenance Personnel for the new Facility. Behind our innovation…There’s you Degree in Engineering, Pharmacy, Chemistry or Chemistry Engineering Approximately 10 years of project management experience, preferably within pharmaceuticals or life sciences, particularly in API manufacturing and biotech requirements. Experience in managing complex projects, budgets, timelines, and Broad technical knowledge of the Various Engineering Disciplines in the Pharmaceutical environment, both on clean and black utilities, process and packaging equipment, automation, Instrumentation and Civil Engineering Strong project management skills encompassing principles, methodologies, and best practices, including planning, scheduling, budgeting, risk management, and change control. Able to handle multiple projects concurrently. Proficient in various engineering disciplines within the pharmaceutical environment, including utilities, equipment, automation, instrumentation, and civil engineering. Strong knowledge of quality assurance, cGMP, DS, DP manufacturing, GMPs, and FDA regulations. Familiar with Lean methodologies and Value Engineering. Proficient in software such as MS-Word, Excel, Autocad, Product Design Specification (PDS), and project management tools (e.g., MS Project), with PPM experience being a plus. Ability to lead project teams, motivate team members, foster collaboration, and resolve conflicts to ensure a cohesive and productive working environment. Task orientated, analytical person who is very comfortable working towards set objectives and has a track record of achieving results in this regard. Strong ability to plan, organize and set priorities. Team player happy to be in an international and multicultural environment, with a track record of achieving results in a cross-cultural environment, open to international and multicultural settings, willing to travel for business and relocate as needed Excellent communication and presentation skills and able to communicate with stakeholders at all levels. Good knowledge of various types of pharmaceutical dosage form, in particular sterile products. Good command of English, French and any other language (verbal & written) Proficient in negotiating and influencing stakeholders to achieve project objectives and secure resources. Strong commitment to ethical practices and compliance with organizational values and standards. People come first at Ferring Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role Parental leave for both birthing and non-birthing parents Extended support on family building journey Making a difference in the lives of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You. Behind our purpose… There’s you If our mission and your vision are aligned, please apply! We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status. Location: Switzerland HQ - St-Prex Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical group committed to helping people around the world build families and live better lives. Ferring is a leader in reproductive medicine and maternal health, and in specialty areas within gastroenterology and urology. Ferring employs over 7,000 people worldwide. The company has operating subsidiaries in more than 50 countries and markets its products in over 100 countries. Learn more at www.ferring.com, or connect with us on us on Twitter, Facebook, Instagram, LinkedIn and YouTube. At Ferring, we'll give you the tools to shape a career build on purpose. Join us and help People around the world to build families and live better lives. Empowerment We create leaders and entrepreneurs We empower, we boost our teams, we incite learning. Innovation We experiment and build our future We search for new solutions, we take risks for innovation, we learn. Accountability We own everything we do with courage We seize responsibilities, we are accountable for our decisions. Collaboration We are in this together We work together across teams, functions and geographies. Transparency We listen and share We communicate honestly, we do it often, we make it simple. Purpose We share one Mission, we are guided by the Ferring Philosophy We know why we are here, we inspire each other. Don't see the dream job you are looking for? Drop off your contact information and resume and we will reach out to you if we find the perfect fit!Über das Unternehmen:ferring

Company / Business Unit: Hamilton Medical AG more information Responsibilities: Hamilton Medical is seeking a highly skilled and experienced Project Leader to be an integral part of our team and play a pivotal role in leading the FDA approval process of our technology. The Project Leader at Hamilton Medical AG will be responsible for defining the plan and organize the project, including efficient management of resources and budget throughout the cycle of the medical device’s approval process starting from technical documents preparation and/or revision, including Clinical Trial Management up to securing FDA approval. You will work closely with cross-functional teams (CRO, R&D, Regulatory, Clinical Affairs and Clinical Research) to ensure our products meet global regulatory standards, enabling us to provide safe and effective solutions to healthcare providers and patients. Join our team in making a positive impact on healthcare worldwide. Your tasks, which you can perform office-based with a possibility of up to 60% home office after a 3-month probationary period, include the following: Develop project plan, set goals and budget as well as identify and manage resources. Monitor, track and report on progress and performance, including budget. Partner with external stakeholders to ensure robust collaboration, Clinical Research Organizations (CROs) and Key Opinion Leaders (KOLs). The initial focus of this role will be to ensure that technical files and clinical trial submission package are compiled and ready for 510K, de Novo, IDE and PMA submissions. Compliance Oversight: Maintain compliance with relevant regulations, standards, and guidelines throughout the development of clinical trial documentation and conduct of the clinical trial. Assist in preparing response to US regulatory authorities’ questions within assigned timelines. Describes and recommends strategies to senior management for earliest possible approvals of clinical trials applications in US in close collaborations with our Regulatory team. Ensures that submission packages are ready for clinical trial site ethics review board/FDA applications for investigational device trial(s). Ensures and contributes to the development of interim or final reports for trial site ethics boards/FDA review/submission, coordinates review processes. Will serve as main point of contact in case of involvement of a CRO for clinical trial management and will oversee document development for clinical trial submission, conduct and close out. Will be responsible for CRO selection, contract management and evaluation. Will be leading Project Team (P-Team): providing functional expertise and leading P-Team. defining and executing strategic implementation plans. interfacing with other workstreams and cross-functional stakeholders. Performs coordination and preparation of document packages for audits and inspections from all areas of company in close collaboration with regulatory team input to minimize potential for findings of non-compliance. Qualifications: Bachelor's degree in a relevant scientific or equivalent in one of the disciplines related to clinical practice/health care, life sciences, or medical device development. Knowledge of FDA regulations (21 CFR 812, 814 and 820), ISO standards (ISO 13485: 2016, ISO 14971: 2019, ISO14155:2020), Regulation (EU) 2017/745. Proficiency in clinical trial management Class III or Class IIb - (EU) 2017/745 or IDE 21CFR 812. Minimum of eight years of Project planning, risk management, time management and other project management skills in the medical device industry . Ability to work collaboratively in a cross-functional team environment. Project management qualification (PMP), Certified associate in project management (CAPM), or equivalent experience as a project manager. Excellent communication skills. Problem-solving and leadership skills. Contract negotiation and conflict resolution experience Project planning, risk management, time management and other project management skills. Fluency in the English language; German and any other language is an advantage. Applications will be accepted until mid-February (15.02.2024). We look forward to receiving your documents! Are you interested? Then please apply online by clicking on the \"Apply\" button. If you have any questions, please do not hesitate to contact [email protected] with the following details: Reference: JR-2918-fjm/Contact: Julius Thomann Applications by post or e-mail can unfortunately not be considered. For more information on employment conditions at Hamilton, such as development opportunities and benefits, please visit our career page https://jobs.hamilton.ch/en/. «We drive innovation to improve people’s lives.» Improving and saving lives: that and nothing less is what Hamilton does - during and outside of pandemic times. As a leading and internationally active high-tech company in the life science sector, Hamilton drives state-of-the-art innovations in the development and production of intelligent respiratory equipment, laboratory robots, biopharma sensors, sample management solutions and other precision instruments. Our customers are hospitals, laboratories, research and industry around the globe. In addition, Hamilton has a strong presence in the growth markets of genetics, robotics, food and environment. The group currently employs around 3,000 people worldwide, more than half of them in Bonaduz and Domat/Ems in the beautiful Graubünden Rhine Valley. A further 15 sites are located in Zurich, Basel, Rapperswil, as well as in the United States, China, Romania and seven other countries in Europe. If you have any difficulties with the application or questions, please contact [email protected]. Applications by post or e-mail can unfortunately not be considered.Über das Unternehmen:Hamilton Medical AGWebsite:http://www.hamilton-medical.com

Bei Hamilton erwartet Dich ein dynamisches Umfeld. Wir bieten Dir eine spannende, verantwortungsvolle Tätigkeit in einem interessanten, international expandierenden Hightech-Umfeld. Dein Arbeitsplatz ist im schönen Bündner Rheintal und bietet Flexibilität dank Home-Office.Hierfindest Du einen Überblick unserer Benefits.Anforderungen:Abgeschlossenes Studium als Informatiker oder eine vergleichbare AusbildungAusgewiesene Berufserfahrung in der Entwicklung komplexer Windows Desktop SoftwareErfahrung in der Leitung von Projekten im regulierten UmfeldErfahrung in der Führung von MitarbeitendenSehr gute Deutsch und Englisch KenntnisseEngagierte, kommunikative und umsetzungsstarke PersönlichkeitBist Du interessiert? Dann bewirb Dich bitte gleich hier online mit Klick auf den "Jetzt Bewerben" Button. Für Rückfragen melde Dich bitte unter E-Mail schreiben mit folgenden Details:Referenz: JR-3452-fjb/Kontakt: Susanne BerndonnerBewerbungen per Post oder per E-Mail können leider nicht berücksichtigt werden.AdresseVia Crusch 87402 Bonaduz28.01.2024 80% - 100% Festanstellung Team Leader and Senior Project Leader Software 80 - 100 % (w/m/d)Firma / Business Unit:Hamilton Bonaduz AG - Business Unit RoboticsAufgaben:We drive innovation to improve people's lives! Arbeite mit uns an der Zukunft der Laborautomation.Als Senior Projektleiter bist Du verantwortlich für die Entwicklung innovativer Applikationen zur Programmierung, Steuerung und Optimierung von Labor-Platformen. Du leitest ein internationales Software Projektteam nach modernen agilen Entwicklungsprozessen und unter Einhaltung verschiedener regulatorischer Anforderungen (insbesondere IEC 62304).Leitung eines grösseren Software Projektes im regulierten, medizinischen UmfeldPlanung und Organisation der Aufgaben der TeammitgliederKoordination der Aufgaben mit internationalen TeammitgliedernUnterstützen des agilen EntwicklungsprozessesDokumentationAls Teamleiter bist du verantwortlich für 6 - 8 funktionsübergreifende Teammitglieder (Product Owner und DevOps Software Engineer). Du koordinierst die Aktivitäten deines Teams mit anderen Teams in derselben Organisationseinheit über mehrere Disziplinen.Hier erfährst Du mehr über unsere Liquid Handling Systeme:

Dein AufgabenbereichDu übernimmst die Leitung der anstehenden ERP-Implementierung auf Basis von Microsoft Dynamics, wobei Du bereits vorhandene Microsoft Dynamics Komponenten integrierstDu inspirierst die Projektleiter und Unternehmensleiter, um gemeinsame Ziele mit Begeisterung und Entschlossenheit zu verwirklichenDu kommunizierst aktiv mit dem Auftraggeber und den beteiligten Teammitgliedern, um eine effektive Kommunikation sowohl Bottom-Up als auch Top-Down sicherzustellenIn enger Abstimmung mit dem Applikationsmanagement koordinierst Du die Stakeholder und behältst Qualität, Fortschritt und Budget im AugeDeine SkillsDu bringst einen erfolgreichen Hochschulabschluss in BWL oder (Wirtschafts-)Informatik mit und mehr als 3 Jahre Berufserfahrung in der Leitung von anspruchsvollen ProjektenDie Anwendung von Projektmanagementinstrumenten beherrschst Du souverän und bringst idealerweise Erfahrung in der Microsoft Dynamics Suite mitDu verfügst über Kenntnisse im Changemanagement sowie im Requirement Engineering und setzt diese stetig umLangjährige Erfahrung in der Steuerung von Projekten unter Anwendung von Azure DevOps und agilen Projektmethoden (Agile, CMMI, SCRUM) runden dein Profil abDeine Deutschkenntnisse sind verhandlungssicher und Du beherrschst auch die englische Sprache gutBenefitsHomeofficeAttraktive Weiterbildungs- und EntwicklungsmöglichkeitenKomfortables Büro mit moderner InfrastrukturInteressante und abwechslungsreiche Tätigkeiten/ProjekteEingespieltes und dynamisches Team

Leitung eines grösseren Software Projektes im regulierten, medizinischen Umfeld Planung und Organisation der Aufgaben der Teammitglieder Koordination der Aufgaben mit internationalen Teammitgliedern Unterstützen des agilen Entwicklungsprozesses Dokumentation Als Teamleiter bist du verantwortlich für 6 – 8 funktionsübergreifende Teammitglieder (Product Owner und DevOps Software Engineer). Du koordinierst die Aktivitäten deines Teams mit anderen Teams in derselben Organisationseinheit über mehrere Disziplinen. Hier erfährst Du mehr über unsere Liquid Handling Systeme: Bei Hamilton erwartet Dich ein dynamisches Umfeld. Wir bieten Dir eine spannende, verantwortungsvolle Tätigkeit in einem interessanten, international expandierenden Hightech-Umfeld. Dein Arbeitsplatz ist im schönen Bündner Rheintal und bietet Flexibilität dank Home-Office. Hier findest Du einen Überblick unserer Benefits. Anforderungen: Abgeschlossenes Studium als Informatiker oder eine vergleichbare Ausbildung Ausgewiesene Berufserfahrung in der Entwicklung komplexer Windows Desktop Software Erfahrung in der Leitung von Projekten im regulierten UmfeldErfahrung in der Führung von Mitarbeitenden Sehr gute Deutsch und Englisch Kenntnisse Engagierte, kommunikative und umsetzungsstarke PersönlichkeitArbeitsort: 7402 Bonaduz Home Office möglichBist Du interessiert? Dann bewirb Dich bitte gleich hier online mit Klick auf den "Jetzt Bewerben" Button. Für Rückfragen melde Dich bitte unter [email protected] mit folgenden Details: Referenz: JR-3452-fjb/Kontakt: Susanne Berndonner Bewerbungen per Post oder per E-Mail können leider nicht berücksichtigt werden.BewerbungsservicesBewerber-Cockpit anlegenZum RatgeberZurückZurückwww.suedostschweizjobs.chHamilton Bonaduz AGTeam Leader and Senior Project Leader SoftwareZurückJetzt Bewerben12.01.2024Team Leader and Senior Project Leader Software7402BonaduzFestanstellung 80-100%Home Office Merken druckenMeinen Arbeitsweg berechnen Jetzt BewerbenJetzt BewerbenBewerbungsservicesBewerber-Cockpit anlegenZum Ratgebermehr Infos zu diesem JobTeam Leader and Senior Project Leader SoftwareAufgaben: We drive innovation to improve people's lives! Arbeite mit uns an der Zukunft der Laborautomation. Als Senior Projektleiter bist Du verantwortlich für die Entwicklung innovativer Applikationen zur Programmierung, Steuerung und Optimierung von Labor-Platformen. Du leitest ein internationales Software Projektteam nach modernen agilen Entwicklungsprozessen und unter Einhaltung verschiedener regulatorischer Anforderungen (insbesondere IEC 62304).

At Sulzer, you are empowered to deliver superior results. As a pioneer in industry we have a proud heritage of innovation and continue to evolve for the future. Join our story and create your own impact by developing your expertise and building solutions that help make our lives safer, smarter and more sustainableSenior Project Controller CT_HQ & SBD-E122 Senior Project Controller - Full Time - Winterthur, Switzerland At Sulzer, you are in charge of your career and continued development. Take the opportunity to broaden your skills by seeking new roles that reflect your experience. Create your own impact by building solutions that help make lives safer, smarter and more sustainable. Join our team within Chemtech division in Switzerland as Senior Project Controller to help us take Project Controlling to the next level. Your main tasks and responsibilities: Globally manage all financial aspects of the individual projects/contracts Support Project teams in organizing the contacts with banks and any financial institution to execute contracts in compliance with Sulzer rules Support foreign exchange hedging, bonds and guarantees Optimize Project cash and manage foreign currency risk Perform pertinent analysis on financial data (achievements, target, forecasts) to help ensure achievement of Project objectives and propose appropriate solutions to mitigate risks Ensure that Project Reviews are held in accordance with relevant procedures and ensure consistency and compliance with Sulzer accounting rules Properly account for risks in the Project financials Build the contract accounting, including cash, based on data collected through ERP systems and from data on the Projects Liaise with accounting for correct revenue recognition Ensure reporting consistency with operations / manufacturing / sourcing, including participating entities Properly report risks, opportunities, and mitigation plans, as well as monitor the cash flow of the contracts Help build Business forecasts, based on the forecast of their individual Project(s) What you bring to Sulzer: Degree in Finance or a related field Proven experience with 10+ years Experience in project accounting, project cost planning, scheduling, and reporting Strong business partnering; proper oral and written communication is a must Strong analytical and problem-solving skills Good project background and technical writing skills IT Skills: MS Office, SAP a must What we offer you : Above average holiday entitlement Attractive pension scheme Employee Assistance Program On-site car parking Access to a wide range of discounts on Everyday Shopping, Entertainment and Lifestyle No visa or work permit support can be provided for this role. Have a question about the role? Reach out to Mirjam Städeli at Write an email. We are looking forward to hearing from you! Sulzer is an equal opportunity employer. We believe in the strength of a diverse workforce and are committed to offering an inclusive work environment. At Sulzer, you are empowered to deliver superior results. As a pioneer in industry we have a proud heritage of innovation and continue to evolve for the future. Join our story and create your own impact by developing your expertise and building solutions that help make our lives safer, smarter and more sustainable We are proud to be recognized as a Top Employer 2023 in Brazil, China, Switzerland, the United Kingdom and the United States. Come and join our story!