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Gehaltsübersicht für System in Kaiseraugst

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Gehaltsübersicht für System in Kaiseraugst

13 440 ₣ Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "System in Kaiseraugst"

Währung: CHF USD Jahr: 2020
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der System Branche in Kaiseraugst

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Kaiseraugst

Währung: CHF
Das Balkendiagramm vergleicht das Durchschnittsgehalt für die Abfrage "System" mit dem Durchschnittsgehalt in den Verwaltungszentren des letzten Monats.

Empfohlene Stellenangebote

Utilities Manager
Randstad (Schweiz) AG, Kaiseraugst
Do you want to work in a big pharmaceutical company? Do you have a first experience in GMP environment in production? You should then read the following lines!Our client, based in Kaiseraugst, is looking for a Utilities Manager for a 1 year contract. Das Team Utilities als Teil des Supportbereichs ES&T (Engineering, Science and Technology) ist verantwortlich für die Instandhaltung der Produktionsgebäude und für die Sicherstellung der zugehörigen Medienversorgung unter Einhaltung aller regulatorischen Vorgaben. Ziel ist die bestmögliche Unterstützung der Wertströme um eine unterbruchsfreie Produktion zu ermöglichen. Aufgaben & Verantwortlichkeiten:• Ansprechpartner für alle Belange betreffend Medien- und Reinstmedienversorgung (z.B. Lüftungsanlagen, WBI/WFI Anlagen, Reinstdampferzeugung, Stickstoff) für die Produktionsgebäude.• Erstellung/Überarbeitung von Standard Operating Procedures (SOPs) und zugehörigen GMP-Dokumenten.• Sicherstellung der Verfügbarkeit von Infrastruktursystemen.• Beurteilung und Bearbeitung von Änderungen, Abweichungen sowie korrektiven und präventiven Massnahmen.• Vorbereitung, Begleitung und Nachbereitung von Behördeninspektionen und Audits.• Bereitschaft für das Arbeiten in einem selbst organisierten Team mit hohem Mass an Eigenverantwortung in einem offenen und kollaborativen Umfeld.• Einbringen und Umsetzung von Ideen zur Prozessverbesserung unter Anwendung von LPS Methoden und Werkzeugen• Enge Zusammenarbeit mit den Wertströmen, Engineering, Technikabteilungen sowie zahlreichen weiteren internen und externen Schnittstellen zur Erreichung ambitionierter Ziele zur Durchlaufzeit, Qualität, Engagement und Kosten.• Einhaltung aller Sicherheits- und Umweltvorschriften, sowie bewusste Förderung der Betriebssicherheit. Must Haves:• abgeschlossenes naturwissenschaftliches Studium (z.B. Pharmatechnik, Verfahrenstechnik, Gebäudetechnik etc.) oder eine vergleichbare Berufsausbildung mit mehrjähriger Berufserfahrung, idealerweise im Bereich der pharmazeutischen Produktion oder einer nahen Industrie. • Mind. 3 Jahre Berufserfahrung im GMP regulierten Umfeld, idealerweise im Bereich der pharmazeutischen Produktion. • Berufserfahrung im Bereich Medienversorgung (z.B. Lüftungsanlagen, WBI/WFI Anlagen, Reinstdampferzeugung etc.) • Berufserfahrung mit internen GMP-Audits oder Inspektionen der Gesundheitsbehörden ist von Vorteil• Kenntnisse und überzeugter Einsatz bezüglich Prozessverbesserungen (z.B. Lean Production System) sowie Agile Management sind von Vorteil• Sehr gute MS-Office Kenntnisse. Kenntnisse in SAP, CONDOR und Trackwise sind von Vorteil.• Sehr gute Deutschkenntnisse in Wort und Schrift werden vorausgesetzt, Englisch ist von Vorteil.• Ein teamorientierte Denkweise mit Blick auf stete Verbesserung der Prozesse und die Fähigkeit in einem sich ständig veränderndem Umfeld konstante Leistung auf hohem Niveau zu erbringen• Fähigkeit und Offenheit, die Chancen und die Vorteile von Veränderungen zu erkennen und zu leben• Hohe Teamfähigkeit und Lösungsorientierung sowie kollaborative Arbeitsweise Do not waste any minutes, apply now! We are looking forward to receiving your application in German.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
Hochschulpraktikum in Quality Systems (ab Frühjahr 2022) - RiKO
Roche, Aargau, Kaiseraugst
An unserem Standort Kaiseraugst bieten wir im Frühjahr 2022 viele spannende Praktikumsmöglichkeiten an. Um mehr über das Produktionszentrum Kaiseraugst und unser Angebot zu erfahren, besuchen Sie gerne unsere Internetseite: careers.roche.ch/riko.Roche Kaiseraugst ist ein Eckpfeiler im weltweiten Produktions- und Logistiknetz von Roche. Über 1900 Personen sind hier beschäftigt, und der Standort beherbergt den grössten und innovativsten Verpackungsbetrieb von Roche weltweit.Mit dieser Ausschreibung bietet der Fachbereich Quality Systems ein Praktikum an, welches sich primär an Studierende aus dem Bereich Pharmazie, Naturwissenschaften, Life Sciences oder Ingenieurswesen richten, für eine Dauer von mindestens 6 Monaten. Sie unterstützen das Team tatkräftig bei der Bereitstellung, Unterhaltung und Weiterentwicklung der pharmazeutischen Qualitätssysteme an den Standorten Kaiseraugst und Basel.Als Praktikant in Quality Systems erwarten Sie im Wesentlichen folgende AufgabenMitarbeit im Rahmen von Quality Risk Management, Technical Change Management, Corrective and Preventive Action Management und Discrepancy Management SystemMitarbeit im Bereich Records Management zur Unterstützung des Standortes bei der korrekten Verwendung und Ablage von elektronischen und physischen RecordsMitarbeit in der lokalen Implementierung von globalen Vorschriften durch Pharmaceutical Quality System (PQS)Mitarbeit bei der Auswertung von QualitätskennzahlenAutomatisierung von Datenabfragen und entsprechende Visualisierung der Daten Ihr ProfilSie sind offen für neue Ideen und hinterfragen konventionelle Denkmuster. Sie schätzen es, in einer leistungsorientierten Umgebung zu arbeiten, die von gegenseitigem Respekt, Diskussion und Zusammenarbeit getragen wird. Dann ist Roche für Sie der Ausgangspunkt für ein spannendes und internationales Arbeitsumfeld mit vielfältigen Entwicklungschancen.Sie sind im Feld der Pharmazie, Pharmatechnik, Naturwissenschaften, Life Sciences, Ingenieurwesen oder verwandte Richtungen zu Hause und überzeugen durch eine offene, kontaktfreudige Persönlichkeit. Zudem sind Sie an einer Universität oder Fachhochschule immatrikuliert.Überdies runden Sie Ihr Profil mit folgenden Kompetenzen ab:Ein hohes Mass an Eigeninitiative und selbstständiger Arbeitsweise sowie schnelles AuffassungsvermögenFreude an der konstruktiven Zusammenarbeit mit internen und externen Stakeholdern sowie an Arbeit in einem dynamischen TeamKreativität, Ideenreichtum und InnovationSie haben Mut und zeigen Risikobereitschaft, neue Wege auszuprobierenIdealerweise bringen Sie bereits Berufserfahrung mit – vorzugsweise im Feld der industriellen ProduktionGute Kommunikationsfähigkeit und PräsentationsskillsDie Bewerbungsfrist für diese Ausschreibung endet Mitte Oktober 2021. Im Anschluss findet ein gemeinsamer virtueller Interviewtag am Freitag 12. November 2021 statt. An diesem Tag laden wir Sie dazu ein einen tieferen Einblick in die Arbeit zu bekommen, die unsere verschiedenen Teams hier täglich verrichten.Das bevorzugte Startdatum des Praktikums ist Frühjahr 2022 oder nach Vereinbarung. Bitte geben Sie Ihr präferiertes Startdatum und die gewünschte Praktikumsdauer in Ihrer Bewerbung an.Sollten Sie bereits Interesse an einem Praktikum im Herbst 2022 haben, machen Sie dies bitte in Ihrer Bewerbung deutlich. Damit Ihre Bewerbung berücksichtigt wird, muss zwingend ein aktueller Lebenslauf und ein Motivationsschreiben eingereicht werden, sowie eine aktuelle Leistungsübersicht.Nicht-EU/EFTA Bürger (m/w) müssen eine Bestätigung der Universität, dass ein Pflichtpraktikum Teil der Ausbildung ist, den Bewerbungsunterlagen beilegen.Bei Fragen prüfen Sie bitte unsere FAQs und Videos unter: careers.roche.ch/faq.More information about career start at Roche you can find hereTags: ROiQQ ROiLS ROiEE ROiTEC RiKO
Hochschulpraktikum in der Quality for Functions Kaiseraugst (ab Frühjahr 2022, 6-12 Monate) - RiKO
Roche, Aargau, Kaiseraugst
An unserem Standort Kaiseraugst bieten wir im Frühjahrssemester 2022 viele spannende Praktikumsmöglichkeiten an. Um mehr über das Produktionszentrum Kaiseraugst und unser Angebot zu erfahren, besuchen Sie gerne unsere Internetseite: careers.roche.ch/riko.Roche Kaiseraugst ist ein Eckpfeiler im weltweiten Produktions- und Logistiknetz von Roche. Über 1900 Personen sind hier beschäftigt, und der Standort beherbergt den grössten und innovativsten Verpackungsbetrieb von Roche weltweit.Die QA for Functions übernimmt vielfältige Aufgaben am Standort Kaiseraugst. Die Aufgabe unseres Teams ist unter anderem die Unterstützung der Freigabe von produzierter Ware im Verpackungsbetrieb, die Unterstützung bei der Qualitätssicherung von aseptischen Abfüllungen (u.a. Antibiotika, gefriergetrocknete Produkte), Unterstützung und Freigabe von Anlagenqualifizierungen und Computer System Validierungen sowie das Sicherstellen der Einhaltung von GMP-Richtlinien und die Genehmigung von ArbeitsvorschriftenAufgrund unserer Schnittstellenfunktion bieten sich für Sie zahlreiche Kontakte im gesamten Herstellungsbereich von Roche Basel und Kaiseraugst.Als Praktikant/in in der QA for Functions (6-12 Monate) können Sie diese oder ähnliche Aufgaben übernehmen: Bearbeiten und Prüfen der Qualifizierungsdokumentation (Qualification/Validation) und weiteren DokumententypenUnterstützen der Quality Assurance Manager, welche die Qualitätssysteme nutzenMitarbeit im Rahmen von Quality Risk Management (QRM), Technical Change Management (TCM), Corrective and Preventive Action (CAPA) Management, Discrepancy Management System (DMS) Durchführung von Datenanalysen und Trendings zu obigen Themen auf AnfrageUnterstützung bei Projekten am Standort KAUUnterstützung der Abteilung bei administrativen Aufgaben und ProjektenSie sind offen für neue Ideen und hinterfragen konventionelle Denkmuster. Sie schätzen es, in einer leistungsorientierten Umgebung zu arbeiten, die von gegenseitigem Respekt, Diskussion und Zusammenarbeit getragen wird. Dann ist Roche für Sie der Ausgangspunkt für ein spannendes und internationales Arbeitsumfeld mit vielfältigen Entwicklungschancen.Sie sind im Feld der Pharmazie, Pharmatechnik, Naturwissenschaften, Life Sciences, Ingenieurwesen oder verwandte Richtungen zu Hause und überzeugen durch eine offene, kontaktfreudige Persönlichkeit. Zudem sind Sie an einer Universität oder Fachhochschule immatrikuliert und haben besonderes Interesse Qualitätsmanagement und präzisen und effizientem Arbeiten, Stakeholdermanagement und enger Kollaboration mit Kollegen auf Augenhöhe. Idealerweise bringen Sie darüber hinaus Vorerfahrung mit GMP-gerechtem Arbeiten im Pharma-Umfeld mit.Überdies runden Sie Ihr Profil mit folgenden Kompetenzen ab:Sehr selbstständige und strukturierte Arbeitsweise Ein hohes Mass an Eigeninitiative und schnelles AuffassungsvermögenFreude an der konstruktiven Zusammenarbeit mit internen und externen Stakeholdern sowie an Arbeit in einem dynamischen TeamKreativität, Ideenreichtum und InnovationSehr gute Englisch- und Deutschkenntnisse Gute Kommunikationsfähigkeit und PräsentationsskillsDie Bewerbungsfrist endet am 18. Oktober. Im Anschluss zur Bewerbung findet ein gemeinsamer virtueller Interviewtag am Freitag, 12. November 2021 statt. An diesem Tag laden wir Sie dazu ein, einen tieferen Einblick in die Arbeit zu bekommen, die unsere verschiedenen Teams hier täglich verrichten.Das bevorzugte Startdatum des Praktikums ist Frühjahr 2022 oder nach Vereinbarung. Bitte geben Sie Ihr präferiertes Startdatum und die gewünschte Praktikumsdauer in Ihrer Bewerbung an.Sollten Sie bereits Interesse an einem Praktikum im Herbst 2022 haben, machen Sie dies bitte in Ihrer Bewerbung deutlich. Damit Ihre Bewerbung berücksichtigt wird, muss zwingend ein aktueller Lebenslauf und ein Motivationsschreiben eingereicht werden, sowie eine aktuelle Leistungsübersicht.Nicht-EU/EFTA Bürger (m/w) müssen eine Bestätigung der Universität, dass ein Pflichtpraktikum Teil der Ausbildung ist, den Bewerbungsunterlagen beilegen.Bei Fragen prüfen Sie bitte unsere FAQs und Videos unter: careers.roche.ch/faq.More information about career start at Roche you can find hereTags: ROiQQ ROiCH ROiDS ROiMB ROiPS ROiCE ROiBE RiKO
Cross Pharma Informatics Solution Architect
Roche, Aargau, Kaiseraugst
Cross Pharma Informatics (xPiX) provides technology experts and talents to the Roche Pharma Organisation. Our strategy to deliver 3-5 times the number of medical advances at 50% less cost to society. Therefore we are accelerating the use of digital technologies and data insights to make significant strides to reach the full potential of better health outcomes for patients and to interact seamlessly with our customers. We are seeking a mission-driven, ardent, self-starting, creative individual to join us in this effort.The Senior Solutions Architect is responsible for designing the functional and technical integration solutions to onboard them onto our common Digital Platform. Responsible for participating in requirements analysis and decomposition, designs and the documentation of the solutions within the Digital Ecosystem. Understand how applications work to support business requirements in alignment with the architecture principles and standards. Works with specialised tools, such as application programming interfaces (APIs) and Event-Driven-Architecture, identity federation or interoperability standards made specifically to support our digital assets.Job Purpose:Participate in the definition of the architecture roadmap for an ecosystem of digital solutions;As a Solutions Architect, you do more than just sketch a system. You work with Engineers, Product Managers, Business Analysts and Product Owners to recommend the best solutions that scales, are reliable and evolve according to our vision, in compliance with the data privacy and legal requirements;Define the best technical solution to integrate different applications and systems using the standard components of our architecture landscape, detecting potential gaps or required improvements in these architecture components;Support the development and business teams on architecture and technical questions, facilitating the service delivery;Proactively foster the delivery of high-quality maintenance, enhancements, and project initiatives of Roche Diabetes Care Platform;Ensure that the architecture components are reusable as much as possible, aligned with the standards and best practices;Works in a multi-project, multi-team environment with both internal and external team members.Understand and analyze non-functional requirements, depending on the nature of a project, including security, privacy and performance requirements. Provide solutions to mitigate the identified risks.Key Accountabilities:Analyse requirements including data, integration requirements, and system interfaces;Assure the system fits the platform, is designed for reuse and integrates with the solutions ecosystem;Evaluate and undertake impacted analyses on major design options;Ensure that the system design balance functional, service quality, security and system management requirements;Design, maintain and manage the interface models, frameworks and artefacts;Contribute to solution scoping and effort sizing with cross-functional teams;Investigate operational requirements, problems and opportunities for cross functional initiatives;Contribute to operational relationship with third party suppliers and consultants;Ensure the quality of our Architecture Documentation.Key skills and Experience:5+ years as Solution Architect in a medium/large company;2+ years relevant experience in cloud native applications using Microservice architecture and Event-Driven design using REST APIs frameworks;Experience working in regulated environments is a plus;Manage the non-functional requirements of a Project;Experience understanding customers/business requirements and building integration solutions;Experience in integration using Async or Sync interfaces using ESB, Web services, REST API or streaming APIs;Proficient in software development lifecycle in Agile frameworks;Ability to identify problems and suggest mitigation and contingency actions;Good communication skills and excellent team collaboration;Experience working with globally distributed teams and 3rd party vendors;Strong sense of ownership, urgency and drive;BS degree Computer Science or related field.
IT Business Partner - Product Development Informatics Quality
Roche, Switzerland, Aargau, Kaiseraugst
At Genentech and Roche, we are accelerating the use of data insights and digital technologies to make significant strides to reach the full potential of personalized healthcare.As a Compliance IT Business Partner, you will join our diverse informatics community of smart, fun, wholehearted, and engaged professionals from various functional areas. You will share our community values of passion, courage, integrity, and gratitude -- all in service of our mission, “doing now what patients need next.”Your primary accountability is to provide quality leadership. By being embedded in Product Development strategy teams you develop a deep understanding of safety, clinical, and medical data challenges and opportunities. You will drive the design, creation, and adoption of novel validation strategies needed for advanced technologies. You ensure data integrity and patient confidentiality while taking measured risks to bring speed to the product development lifecycle. You act as a bridge between technology and compliance groups. As the Compliance Business Partner, you will establish strong relationships and manage stakeholders across the globe. You are someone who can negotiate, influence, and lead at all levels.Your responsibilities include: Articulate and facilitate the understanding of a system’s intended use and it’s compliance risk profileOversee and provide guidance and consultancy on Information governance and compliance topics Information lifecycle review , retention management, disposal management, legal hold, metadata standards, data sharing principles, data privacy (SCC's, Privacy Shield, Data location), vendor qualification / audit, manager vendor risk and platform SRA/DCR (boundaries to projects, common elements, alignment)Risk-based identification and classification of GXP systemsGuide software project and product teams in understanding their role in establishing and maintaining the compliance of critical systems.Drive quality simplification and transparency across the organizationHave expert-level knowledge of SDLC life cycle methodologies, including agile, and be able to apply agile to compliance topics. Review & approve system risk assessments (SRA)Advise advanced analytics data groups on future compliance trendsServe as a point of escalation to executive leadership and PDQ for quality and compliance issues related to high-risk systems. Leverage the technical expertise of the internal teams and external technology providers and vendors to deeply understand the picture and riskEngage with Procurement on acquisitions and assess compliance against internal expectation and SOPs’ and assess outsourced vendors and clinical suppliers. Oversee data classification and privacy for all PD systems and serve as a single point of contact for PDIX on audit and inspection Maintain expert-level knowledge of the dynamic health authority governance; inclusive of GDPR, HIPAA, SaMD, 21CFR part 11.Who you are:Has a diverse background. Has managed change in the most trying of times. Is a fixer and a solver. Wants to tackle the biggest healthcare challenges that face us globally in the 21st century. They excel at relationship building and networking. Have demonstrated the ability to navigate complexity, be pragmatic, and prioritize!As ideal candidate you have a BA or BS in life science, informatics, business or equivalent. MA or MS and post-graduate coursework is desirable. Further more you bring at least 10 years of related experience, domain knowledge of the pharmaceutical industry and manufacturing/quality assurance processes and systems, computer systems validation, GXP, FDA Part 11, HIPPA, SaMD, Data Privacy.Your further qualifications:3+ years in a technology role IT or DataProgram or IT Product management experienceExpert knowledge of Software Development Life Cycle methodologies, inclusive of Agile. Experience leading cross-functional collaborative team environments, provide innovative solutions to complex business problems and make decisions with cross-functional impactStrong English and German communication skills (nice to have) -- ability to communicate complex information, issues, and potential solutions at an executive level. Ability to travel up to 25%Roche embraces diversity and equal opportunity in a serious way. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be. If you still have questions then please check our FAQs and videos on careers.roche.ch/faq.
Senior Test Manager
ITech Consult AG, Kaiseraugst, Rheinfelden
Project: For our customer a big pharmaceutical company situated in Kaiseraugst we are searching for a highly qualified Senior Test Manager (f/m/d) Background: The company has initiated a global Business Process and ERP Program, which will define, implement and deploy the Future ERP solutions based on SAP S/4HANA and other cloud and on premise systems, supporting simplified, standardized and automated global business processes by leveraging SAP industry best practices. To support us on this journey, specifically in the area of a global procurement cloud-based solution, we are looking for an experienced and strategic test professional with relevant experience in the Life Science industry. The ideal candidate will support our implementation and deployment efforts regarding a sustainable test strategy and solution quality approach. Tasks & Responsibilities: Define the approach for the test preparation, planning, execution and coordination in close collaboration with Test Manager / Coordinators, Project and Deployment Leads Drive continuous improvements and efficiencies of the test management strategy, approaches, tools and foster integrated ways of working (e.g. with scrum and deployment teams) in close alignment with Project Leads, Program Test Lead and Implementation Partner Enabling a team of Test Managers and Coordinators who execute the testing and report progress. Define appropriate education needs / prerequisites for all teams involved in the testing, Advocating the appropriate level of quality by defining and implementing a holistic test strategy incorporating all aspect of the solution and implementation (e.g. product development/enhancement, data and configuration, localization, regression and E2E Testing) Define KPIs & SLAs for the test preparation, execution and defect management across all areas involved in the myBuy Program. (scrum and deployment teams) Define template(s) to track the test readiness & progress (E2E) Plan & Forecast testing activities across the mid-level and deployment plans aligned with our partner systems. Analyse and implement management improvement processes in alignment with the project leads. Must haves: . 5 years of experience as a Test Manager, including definition and implementation of a test strategy for a global solution Experience in a regulated environment, preferred in the pharmaceutical or medical device industry 10 years of relevant experience in global and complex system implementation projects as a core team member Strong Project management and Planning skills in waterfall and agile approaches Experience in working with SAP Solution Manager and JIRA Familiar with CSV practices (no certification required) Business level fluency in English both written and verbal, German is an advantage Strong communication skills is a must Strategic and system thinking with a view to long-term sustainability Strong listening, facilitation and collaboration skills Requires excellent problem solving and analytical skills to resolve a variety of routine and complex issues and challenges Proven capability in negotiation, conflict resolution and stakeholder management Flexibility to work outside of normal working hours to support global projects Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com. Contact us for further information regarding our company, our positions or our attractive payroll-only-program: 41 41 760 77 01. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed. ITech Consult Recruitment The Old Station House 15a Main Street Blackrock Co. Dublin A94 T8P8 Ireland Type Duration Description cookielawinfo-checkbox-necessary session 1 year Records the default button state of the corresponding category. It works only in coordination with the primary cookie. cookielawinfo-checkbox-non-necessary session 1 year viewed_cookie_policy session 1 year Is the primary cookie that records the user consent for the usage of the cookies upon accept and reject. It doesn't track any personal data and is set only upon user action (accept/reject). _ga third party 2 years This cookie is installed by Google Analytics and collects information on how users interact with the website. The cookies store information anonymously and assigns a randomly generated number to identify unique visitors. It is used to distinguish users. _gat third party 1 minute Google Analytics cookies to track users as they navigate the website and help improve the website's usability. _gid third party 24 hours This cookie is installed by Google Analytics and collects information on how users interact with the website. The cookies store information anonymously and assigns a randomly generated number to identify unique visitors. It is used to distinguish users.
Materials Planning and Scheduling Business Analyst
ITech Consult AG, Kaiseraugst, Rheinfelden
Materials Planning and Scheduling Business Analyst (m/f/d) Materials Planning and Scheduling Business Analyst (m/w/d) – SAP / Project leader / Requirement / English Background: Background: The PT PLAN workstream member is supporting the group wide ASPIRE program. The workstream member is a core member of the PT PLAN work-stream, driving the ASPIRE Supply Chain Planning (SCP) project. The workstream member is supporting the transformational change for assigned Supply Chain Planning processes in scope to implement aligned and harmonized end-to-end processes and related systems landscape as well as enable the necessary organization in PT. The change combines process harmonization, system standardization, increased automation and people change management. The workstream member is ensuring that LPS elements and methods are applied. The workstream member develops approaches to drive towards our Supply Chain Planning vision of „higher quality decisions“, e.g. by ensuring single data captured at source-systems, standardized data structures, simplified business processes, increased automation, etc. The workstream member does report to the PT PLAN workstream. Close collaboration with the business function and across other workstreams is key for the role. Perfect Candidate: This position is open to backfill an internal role. We are looking for a dynamic candidate with a University Degree in Business or IT and a first experience in material planning (between 3 to 5 years). Experience with SAP planning application is required (APO or MP). Experience in pharma or with Factory Scheduling is an advantage. On a soft skill note, we are looking for someone eager to learn and develop him/herself into the role. Tasks & Responsibilities: Defines with the Work Stream Lead the activities to be performed and related effort. The focus of this role will be in Material Planning (MP) and Master Production Scheduling (MPS) business process areas within the Plan work stream Lead the delivery of assigned work packages according to schedule, and report regularly accomplishments to the work stream lead. This includes but not limited to: – Coordinates all activities to assure excellence and a high level of standardization in future process & system design (to-be-picture, fit-for-purpose) – Works together with the BPO / BPM / SME community for re-designing the PLAN processes as well as for relevant enabling processes (e.g. Data) as applicable – Works closely with other business process areas to assure E2E process excellence – Defines business requirements and translates business needs into user requirements – Provides expertise and guidance for defining planning relevant master data – Ensures that the final business process and systems design / architecture meet the overall functional requirements – Collects feedback from the voice of customers, evaluates pain points based on the current systems & process landscape, compiles improvement opportunities – Ensures that the technical data specification for migration is provided – Works closely together with IT for solution definition – Ensures appropriate user acceptance testing – Test case, Transition plans & Training development, documentation and execution – Translate core project design principles for his own area of responsibility. Must Haves: – University Degree in business or IT – 3-5 years of experience in Material Planning (MRP) – Deep experience with SAP Planning tools such as SAP APO, MM, OMP – Fluent English, excellent oral and written communication and presentation skills – Project leadership experience – Demonstrated delivery focus and execution – Ability to translate 10y requirements into design – Knowledge of financial and management accounting fundamentals – Strong knowledge of data lifecycle management and can drive organizational commitment to a data ownership mindset. – Use quantitative and qualitative approaches to solve business problems – Ability to influence at all levels – Deeply curious and energized by learning; can coach new skills and behaviors Reference No.: 920665SKN Role: Materials Planning and Scheduling Business Analyst Industry: Pharma Location: Kaiseraugst Workload: 100% Start: ASAP Duration: 12 Deadline : 24.09.2021 Skill Materials Planning and Scheduling Business Analyst (m/w/d) - SAP / Project leader / Requirement / English ITech Consult Recruitment The Old Station House 15a Main Street Blackrock Co. Dublin A94 T8P8 Ireland Type Duration Description cookielawinfo-checkbox-necessary session 1 year Records the default button state of the corresponding category. It works only in coordination with the primary cookie. cookielawinfo-checkbox-non-necessary session 1 year viewed_cookie_policy session 1 year Is the primary cookie that records the user consent for the usage of the cookies upon accept and reject. It doesn't track any personal data and is set only upon user action (accept/reject). _ga third party 2 years This cookie is installed by Google Analytics and collects information on how users interact with the website. The cookies store information anonymously and assigns a randomly generated number to identify unique visitors. 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Global Supply Manager (m/f/d)
Koninklijke DSM N.V., Kaiseraugst, Rheinfelden
Global Supply Manager (m/f/d) DSM – Bright Science. Brighter Living.™ Royal DSM is a global, purpose-led, science-based company active in Nutrition, Health and Sustainable Living. DSM’s purpose is to create brighter lives for all. DSM addresses with its products and solutions some of the world’s biggest challenges while simultaneously creating economic, environmental and societal value for all its stakeholders – customers, employees, shareholders, and society at large. DSM delivers innovative solutions for human nutrition, animal nutrition, personal care and aroma, medical devices, green products and applications, and new mobility and connectivity. DSM and its associated companies deliver annual net sales of about €10 billion with approximately 23,000 employees. The company was founded in 1902 and is listed on Euronext Amsterdam. More information can be found at www.dsm.com . Do you want to be part of a science-based company that has a rich heritage of innovation, successful commercial solutions and sustainability efforts? The Challenge We are looking for a bright, highly motivated Global Supply Manager (m/f/d) to join our Water-soluble Vitamins team within our Global Products & Strategic Alliances unit. The position of Global Supply Manager is core to the DSM Supply Chain and is the central point of the interface between Business and Operations. In this role, you are responsible to match the global demand and supply by managing the global supply planning process for defined product groups and production lines both in the short & mid-long-term horizons. Management of the portfolio, inventory, slow movers, restricted inventory are key elements in the collaboration with key stakeholders throughout the organization (Quality, Sales, Marketing, Sourcing, Production Sites) achieving the balance. The offered position is a full-time assignment, with an ideal starting date from November 2021, located at the headquarters of DNP in Kaiseraugst, Switzerland. The Position Lead the Integrated Business Planning (IBP) process in the development of a plan encompassing the agreed sales, supply and inventory plans, to meet the short- and medium-term sales ambitions of the business Ensure the effective execution of the S&O planning process within APO (or another planning system) at global level and influence the regions to enable an integral supply chain planning in the system Provide input to S&OP meeting with "what if" scenarios to the proposed plan and simulate the effect of various alternatives Give input to definition of inventory levels and define stock policies in agreement with business management and with regional Supply Chain teams Identify and agree supply chain improvement projects with business and suppliers Managing various portfolios and manufacturing desires with KPIs which are potentially conflicting with one and other to yield DSM’s best interest (e.g. OWC vs Idleness or decisions on production when two products are tight) Upgrade of the planning system to rely more on automation and limit manual intervention to manage exceptions. The Global supply manager needs to influence Multiple interfaces (business, suppliers, supply chain, quality etc.) across the organization with a strong need to communicate clearly and influence to get things done The Ideal Ideally, Master of Science in supply chain management, business administration or equivalent Minimum of 3 years’ experience in a planning function Deep systems knowledge of SAP systems Analytical mindset, root cause analysis understanding bigger picture with explanations of details required to engage with key stakeholders Affinity to learn, deal with ambiguity and use new systems and processes Broad experience in stakeholder management: Being able to reconcile conflicting goals with the best overall outcome for DSM Ability to work in multi-functional, multi-disciplinary, and multi-cultural environment and teams (Pro-)active communication, solution oriented, collaborative Excellent communication skills in English. German language skills are beneficial The Reward Working for DSM means the opportunity to really contribute to improve people’s lives and solving the challenges of today’s world. Challenging jobs, career opportunities and an inspiring environment allow you to enhance your personal development. DSM recognizes that the on-going success of the company depends on the continued development and engagement of our employees and pursues a fair and competitive remuneration policy, recognizing individual and team competencies and performance. Procedure & Contact Interested in this position? Please apply on-line by sending us your CV & Motivation letter in English via the career portal (www.dsm.com/careers ). For additional questions, please contact Andrea Beck (Recruitment Business Partner) (andrea.beckdsm.com ). Reference check procedures are part of the DSM Recruitment & Selection Process. You will be contacted when these references checks are required. Royal DSM is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, or any other characteristic protected by law. DSM in 3 minutes Do you know that DSM has the broadest portfolio of nutritional ingredients - that millions of people already have our biomaterials in their body - and that our innovations make materials lighter, healthier, safer, stronger, more durable and have a lower environmental footprint? This short 3 minute video shares our portfolio in Nutrition, Health and Sustainable Living
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