Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Aufbau und Entwicklung von Kundenbeziehungen im neuen Geschäftsbereich Endokrinologie mit Fokus auf Kundenidentifizierung, Aufbau von Kunden Know-how und Entwicklung von Kundenplänen Erfolgreicher Launch im zugewiesenen Gebiet auf Basis der Marketing- und Vertriebsstrategie Verantwortlich für den Vertrieb bestehender Produkte im Bereich Nephrologie mit Umsetzung der vorgegebenen Marketing- und Vertriebsstrategie.
Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Verantwortlich für den Vertrieb bestehender Produkte bzw. der Einführung von biosimilaren Antikörpern in den Bereichen Immunologie Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den Vorgesetzten Besuche der im Zuge des Targeting ausgewählten Zielkunden im niedergelassen, ambulanten und stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung und –steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit der Immunologie Linie und anderen Vertriebslinien (wie Medical Liaison Manager, Healthcare Manager, Hospital) Durchführung von Gebiets-, Wettbewerbs-, Geschäfts- und Kundenanalysen und Anwendung analytischer Instrumente wie Kundensegmentierung, Potentialanalyse, Targeting sowie die Erstellung von Kundenmaßnahmeplänen Wir suchen im Gebiet Würzburg, Coburg, Erlangen, Donauwörth, Schwäbisch Gmünd, Aschaffenburg
Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Verantwortlich für den Vertrieb bestehender Produkte bzw. der Einführung von biosimilaren Antikörpern in den Bereichen Immunologie Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den Vorgesetzten Besuche der im Zuge des Targeting ausgewählten Zielkunden im niedergelassen, ambulanten und stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung und –steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit der Immunologie Linie und anderen Vertriebslinien (wie Medical Liaison Manager, Healthcare Manager, Hospital) Durchführung von Gebiets-, Wettbewerbs-, Geschäfts- und Kundenanalysen und Anwendung analytischer Instrumente wie Kundensegmentierung, Potentialanalyse, Targeting sowie die Erstellung von Kundenmaßnahmeplänen Wir suchen im Gebiet Hannover, Braunschweig, Wolfsburg, Hildesheim.
Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Verantwortlich für den Vertrieb bestehender Produkte bzw. der Einführung von biosimilaren Antikörpern in den Bereichen Immunologie Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den Vorgesetzten Besuche der im Zuge des Targeting ausgewählten Zielkunden im niedergelassen, ambulanten und stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung und –steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit der Immunologie Linie und anderen Vertriebslinien (wie Medical Liaison Manager, Healthcare Manager, Hospital) Durchführung von Gebiets-, Wettbewerbs-, Geschäfts- und Kundenanalysen und Anwendung analytischer Instrumente wie Kundensegmentierung, Potentialanalyse, Targeting sowie die Erstellung von Kundenmaßnahmeplänen Wir suchen im Gebiet Ravensburg, Friedrichshafen, Kirchheim Teck, Freiburg, Reutlingen, Tübingen
Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Verantwortlich für den Vertrieb bestehender Produkte bzw. der Einführung von biosimilaren Antikörpern in den Bereichen Immunologie Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den Vorgesetzten Besuche der im Zuge des Targeting ausgewählten Zielkunden im niedergelassen, ambulanten und stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung und –steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit der Immunologie Linie und anderen Vertriebslinien (wie Medical Liaison Manager, Healthcare Manager, Hospital) Durchführung von Gebiets-, Wettbewerbs-, Geschäfts- und Kundenanalysen und Anwendung analytischer Instrumente wie Kundensegmentierung, Potentialanalyse, Targeting sowie die Erstellung von Kundenmaßnahmeplänen Wir suchen im Gebiet Hannover, Braunschweig, Magdeburg, Bremen, Oldenburg
Mehrjährige erfolgreiche Tätigkeit im pharmazeutischen Außendienst Wünschenswert bestehende Kontakte zum Kundenstamm, insbes. zu wichtigen Schlüsselkunden im Verkaufsgebiet Erfahrungen und/oder grundlegende Kenntnisse im Indikations-Bereich sind ein Plus Sehr gute Kommunikations- und Überzeugungsfähigkeiten mit Stärke im Abschluss und in Verbindlichkeit von Verkaufsgesprächen Selbstsicheres Auftreten im Umgang mit Kunden Hohe unternehmerische Leistungs- und Ergebnisorientierung mit strategischer und analytischer Kompetenz Erfahrung in der Zusammenarbeit mit Medical Liaison Managern und evtl. auch Healthcare Managern Strukturierte und systematische Arbeitsweise mit hoher Selbständigkeit und Eigenmotivation Ausgeprägte Flexibilität und Belastbarkeit mit Bereitschaft zu vermehrter Reisetätigkeit Gute Kenntnisse im MS Office Paket & digitalen Kommunikationstools Ihre Aufgaben: Verantwortlich für den Vertrieb bestehender Produkte bzw. der Einführung von biosimilaren Antikörpern in den Bereichen Immunologie Erreichung vertrieblicher Zielvorgaben wie Marktanteil, Umsatz, Kontaktvorgaben, -frequenz und Gebietsabdeckung, sowie qualitativer Ziele mit regelmäßigem Monitoring und Reporting der verantworteten Ergebnisse an den Vorgesetzten Besuche der im Zuge des Targeting ausgewählten Zielkunden im niedergelassen, ambulanten und stationären Bereich mit effizienter Frequenz, sowie selbständiger, zahlenorientierter Erfolgsmessung und –steuerung Erreichung einer optimalen Vertriebsbreite durch Nutzung von Omnichannel Aufbau und Ausbau von Netzwerk/Beziehungen zu Schlüsselkunden und Meinungsbildnern Enge Zusammenarbeit und Abstimmung mit der Immunologie Linie und anderen Vertriebslinien (wie Medical Liaison Manager, Healthcare Manager, Hospital) Durchführung von Gebiets-, Wettbewerbs-, Geschäfts- und Kundenanalysen und Anwendung analytischer Instrumente wie Kundensegmentierung, Potentialanalyse, Targeting sowie die Erstellung von Kundenmaßnahmeplänen Wir suchen im Gebiet Berlin, Schwedt, Frankfurt/Oder, Guben
Zahlreiche zusätzliche Benefits sind in unserem Unternehmen selbstverständlich:Attraktive Mitarbeiterrabatte über die Plattform Corporate BenefitsEinen anspruchsvollen und abwechslungsreichen ArbeitsplatzHausinterne EntwicklungsmöglichkeitenQualifiziertes EinarbeitungskonzeptLeistungsgerechte VergütungGeregelte Arbeitszeiten (Wochenenden frei) Kontakt Beatrice TraineauClinic Manager Medical Eye‑Care MVZ Nord GmbHTel: +49 (151) 54684826 Auf diese Stelle bewerben Über uns Bergman Clinics ist ein führender Anbieter von fachärztlichen Spezialistenzentren in Europa, mit Hauptsitz in den Niederlanden.
Leading (interdisciplinary) of the core trial teams (e.g.: trial data managers, trial statistician, trial pharmacokinetics and clinical trial manager,…). Leading the Trial Oversight Meeting (as applicable). Collaborating with other functional groups within the client where necessary to support milestone achievement and to manage study issues and obstacles.
Account Manager (d/w/m) - Moderne Wundversorgung Essity ist ein global führendes Hygiene- und Gesundheitsunternehmen. Wir engagieren uns für die Verbesserung der Lebensqualität durch hochwertige Hygiene- und Gesundheitslösungen.
Key Responsibilities Develop study-specific action plans with research sites to accelerate recruitment and support procedural training.Educate healthcare professionals and their staff on study protocols related to clinical trials.Partner with referral networks to identify potential trial participants.Maintain and analyze customer records to tailor strategies for pre-screening, screening, and enrollment.Complete internal reporting and organize group events to optimize program delivery.Address and manage objections effectively.Stay current with technical knowledge in relevant therapeutic areas. Qualifications Registered Nurse, other healthcare professional, or Clinical Research Associate (CRA) required.High flexibility to travel (including internationally if needed).Bachelor’s degree (BA/BS) in Health Sciences or related field, or equivalent qualifications.Located in Germany with fluency in German and English languages.1–2 years of relevant direct experience in working with research sites.Clinical competence in the therapeutic area.Excellent interpersonal and communication skills.Strong written and verbal communication skills.Ability to work independently and coordinate across multiple functions.Solutions-oriented approach and positive attitude.Strong customer service orientation and collaborative mindset.Demonstrates empathy and cultural awareness.Upholds the values of IQVIA and the CTE group.
Allocate payments to correct invoices. Maintain up-to-date customer account balances. Manage deduction approval process. Process credit notes, debit notes, and adjustments. Monitor aging reports and follow up on overdue accounts.
Production Planner Your Tasks Work with Manager to monitor again WIP; exception messages, transactional integrity and long view planning schedules. Using master schedule and various sources, provide production schedule for manufacturing, sub assembly and final assembly department; Responsible for overseeing and handling special projects as required.
Production Planner Your Tasks Work with Manager to monitor again WIP; exception messages, transactional integrity and long view planning schedules. Using master schedule and various sources, provide production schedule for manufacturing, sub assembly and final assembly department; Responsible for overseeing and handling special projects as required.
Job Overview: As an Associate Director, Biostatistics, with regional/site presence, you will manage a team of Biostatistics staff and fulfil the role of site head or functional head within a site. You will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying advanced statistical methods to project work.
Sie wirken bei der Zieldefinition der Projekte mit und definieren Projektmeilensteine sowie Projektphasen.Nach Erstellung und Abstimmung des Projektplans identifizieren Sie Risiken, bewerten diese und leiten geeignete Maßnahmen zur Minimierung ab.Sie steuern regulatorische Anforderungen an unsere Produkte gemeinsam mit externen Dienstleistern.Sie managen interdisziplinäre Projektteams und verantworten die interne sowie externe Projektkommunikation.Sie führen kontinuierliche Soll-/Ist-Vergleiche hinsichtlich Projektzielen durch und bringen Projekte bei Abweichungen strukturiert zurück auf Kurs.Den aktuellen Projektstatus berichten Sie regelmäßig an das Management.Zusätzlich übernehmen Sie perspektivisch auch firmenweite strategische Projekte außerhalb der reinen Produktentwicklung.Sie arbeiten eng mit Entwicklung, Fertigung sowie weiteren Fachabteilungen in Deutschland, China und Vietnam zusammen.Abgeschlossenes Studium im Bereich Elektrotechnik, Mechatronik, Wirtschaftsingenieurwesen oder eine vergleichbare Qualifikation.
Sabbaticals, JobRad, JobTicket und be-triebliche Altersversorgung Förderung von Weiterbildung sowie Entwicklungsperspektiven auch im Rahmen unseres internationalen Netzwerks Ihre Aufgaben Eigenverantwortliches Management und administrative Überwachung von Vertriebsprogrammen, inklusive Sicherstellung der Prozesskonformität und Dokumentationsqualität Unterstützung der Account Manager bei der Vorbereitung entscheidungsreifer Unterlagen und der Abwicklung von Vertriebsfällen Zusammenarbeit mit internen Abteilungen wie Vertragsverwaltung und Risk sowie weiteren Fachbereichen zur optimalen Vertriebsunterstützung Erstellung und Analyse von Programm-Reportings sowie Aufbereitung aller relevanten Daten Übernahme vielfältiger Back-Office-Tätigkeiten zur Unterstützung des Vertriebsteams Proaktive Anpassung und Optimierung interner Prozesse in Zusammenarbeit mit dem Team und anderen Abteilungen Ihr Profil Abgeschlossene Ausbildung im Bankwesen oder ein wirtschaftswissenschaftliches Studium, idealerweise mit Erfahrung in den administrativen Abläufen und Systemen einer Bank Fundierte Kenntnisse im Leasing- bzw.
The Role: Serve as the primary legal advisor for employment law matters across EMEA, with a focus on Germany and Switzerland.Provide strategic counsel on organizational change initiatives, including restructurings and workforce planning.Lead negotiations with works councils and manage complex employment-related projects.Oversee litigation and manage external counsel, ensuring cost-effective and high-quality outcomes.Advise on HR policies, compliance, and internal investigations.Deliver training sessions to HR and business leaders on key employment law topics.
To learn more please visit http://www.convatecgroup.com In der Rolle des National Key Account Manager Advanced Woundcare Handel sind Sie verantwortlich für die strategische Entwicklung und operative Betreuung der wichtigsten Fachhandelskunden auf nationaler Ebene im Bereich der modernen Wundversorgung.
Postgraduate qualification preferred.12+ years of relevant commercial experience in international biopharmaceuticals, including extensive strategic and operational marketingPossesses strong commercial acumen, and the ability to manage multiple priorities, processes, timelines, and expectations across diverse stakeholder groupsExperience in leading strategic processes for portfolio and brand development, including investment and resource allocationExperience leading global marketing initiatives and managing diverse, multicultural matrix teamsExperience in P&L management & ideally as a General Manager requested to realise the value of expected portfolio and brand growthDemonstrated ability to lead, influence and inspire cross-functional matrix teams, driving collaboration, innovation and results at a global, region and local levelProficiency in CRM systems and tools, with a focus on leveraging data-driven insights to drive customer engagement and retentionStrong strategic and analytical capabilities, with the ability to translate market insights into actionable marketing strategies and tacticsExcellent project management skills, with a track record of successfully managing complex, multi-stakeholder projects from inception to implementationAn excellent command of the English language (spoken and written) is required About CSL Vifor CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency and nephrology.
Wir garantieren unseren Kunden eine Produkt-Generationen-übergreifende Kompatibilität. Als Product Manager (m/w/d) verantworten Sie unser Batterieportfolio in etablierten Märkten sowie im stark wachsenden Robotik-Segment. In dieser bereichsübergreifenden Schlüsselrolle treiben Sie aktiv die Weiterentwicklung unseres Produktportfolios voran und gestalten die Zukunft der mobilen Energieversorgung entscheidend mit.
Wir garantieren unseren Kunden eine Produkt-Generationen-übergreifende Kompatibilität. Als Product Manager (m/w/d) verantworten Sie unser Batterieportfolio in etablierten Märkten sowie im stark wachsenden Robotik-Segment. In dieser bereichsübergreifenden Schlüsselrolle treiben Sie aktiv die Weiterentwicklung unseres Produktportfolios voran und gestalten die Zukunft der mobilen Energieversorgung entscheidend mit.
Gemeinsam tun wir alles dafür, dass unser Team auch in Zukunft Optima, das Beste ist. #wecareforpeople Als Service Account Manager (m/w/d) sind Sie Teil von Optima Life Science. Sie wirken bei der Entwicklung und Fertigung intelligenter Turnkey-Anlagen zum Herstellen, Verpacken und Kartonieren von Wundauflagen mit.
Identify and assess new product opportunities, development projects and business fields with a strong emphasis on gynecology/women’s health Lead negotiations for licensing agreements and development partnerships, including coordination of contract drafting Manage cross-functional projects, ensuring alignment of commercial and pharmaceutical requirements Conduct and support patent research, including preparation of risk assessments for upcoming market launches Collaborate closely with international sales affiliates and internal portfolio stakeholders Represent the company at national and international conferences, trade fairs and industry events A completed degree in pharmacy, business administration or a related field Relevant experience in Business Development within the pharmaceutical industry, with a clear focus on gynecology or women’s health portfolio Strong communication skills, a collaborative mindset and the ability to work with diverse stakeholders A proactive, solution-oriented approach with strong resilience in negotiation settings Business-fluent in English, additional languages are an advantage Willingness to travel up to approx. 25% A secure and long-term position within a stable and expanding pharmaceutical organisation Flexible hybrid arrangement, allowing remote work A competitive compensation package incl. additional financial benefits Hybrid working options Extensive opportunities for professional and personal development Gehaltsinformationen An attractive remuneration package awaits you Ihr Kontakt Ansprechpartner Kristine Klein Referenznummer 858726/1 Kontakt aufnehmen E-Mail: kristine.klein@hays.de Anstellungsart Festanstellung durch unseren Kunden
Support procurement processes across all Carve-out phases including due diligence, planning and executionEnsure smooth transition and integration of systems, services and suppliersDevelop and manage strong relationships with key vendors and service providersLead negotiations and manage supplier performance and complianceConduct strategic sourcing and supplier selection based on quality, cost and reliabilityManage contract creation, negotiation and lifecycle governancePerform data analysis to identify cost optimization and process improvement opportunitiesAssess, monitor and mitigate procurement-related risksCollaborate closely with cross-functional stakeholders including IT, Automation, Quality, Finance, Legal and MROMaintain procurement KPIs and develop data-driven performance reports Bachelor’s degree in IT, Business Administration, Supply Chain Management or a related fieldMaster’s degree or relevant certifications (CPSM, CIPS) are an advantageExperience in indirect procurement, ideally in CDMO or pharma environmentsExperience in Carve-out or Divestment activitiesExtensive knowledge in procurement processes, strategic sourcing, vendor and contract managementProven track record in managing procurement streams within business divestmentsStrong negotiation, analytical and problem-solving skillsExcellent communication abilities and stakeholder management skillsProficiency in procurement systems, ERP tools and MS OfficeStrategic thinker, highly organized, adaptable, resilient and collaborative in team settings Opportunity to work on high-impact strategic Carve-out projects within a global CDMOExposure to cross-functional leadership teams and strategic decision-makingInnovative, collaborative and international work environment Ihr Kontakt Referenznummer 863140/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Support procurement processes across all Carve-out phases including due diligence, planning and execution Ensure smooth transition and integration of systems, services and suppliers Develop and manage strong relationships with key vendors and service providers Lead negotiations and manage supplier performance and compliance Conduct strategic sourcing and supplier selection based on quality, cost and reliability Manage contract creation, negotiation and lifecycle governance Perform data analysis to identify cost optimization and process improvement opportunities Assess, monitor and mitigate procurement-related risks Collaborate closely with cross-functional stakeholders including IT, Automation, Quality, Finance, Legal and MRO Maintain procurement KPIs and develop data-driven performance reports Bachelor’s degree in IT, Business Administration, Supply Chain Management or a related field Master’s degree or relevant certifications (CPSM, CIPS) are an advantage Experience in indirect procurement, ideally in CDMO or pharma environments Experience in Carve-out or Divestment activities Extensive knowledge in procurement processes, strategic sourcing, vendor and contract management Proven track record in managing procurement streams within business divestments Strong negotiation, analytical and problem-solving skills Excellent communication abilities and stakeholder management skills Proficiency in procurement systems, ERP tools and MS Office Strategic thinker, highly organized, adaptable, resilient and collaborative in team settings Opportunity to work on high-impact strategic Carve-out projects within a global CDMO Exposure to cross-functional leadership teams and strategic decision-making Innovative, collaborative and international work environment Ihr Kontakt Referenznummer 863140/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Maintain and troubleshoot data integration pipelines to ensure stable data flow into AI and analytics systems Support model development by assisting with training, validation, and optimization of machine learning workflows Conduct data analysis to extract insights and provide clear reports supporting R&D research questions Solve technical challenges related to data access, pipeline performance, and software limitations Ensure continuity of ongoing projects by aligning closely with the core team and delivering on timelines Perform image analysis and prepare datasets required for scientific and ML use cases Manage and improve ETL processes to ensure data quality, structure, and availability Document workflows, pipeline changes, and analytical steps to ensure clarity and reproducibility Academic background in computer science, data science, engineering, or a related quantitative field Strong proficiency in Python with expertise in scientific and analytical libraries Skilled in SQL and working with relational databases Understanding of ETL concepts and practical experience working with data pipelines Solid foundation in machine learning principles and model lifecycle Ability to perform image analysis for scientific or research applications Strong communication and interpersonal skills with the ability to collaborate in a technical team Independent, structured problem-solver with a commitment to clear documentation and FAIR data practices Opportunity to contribute directly to active R&D projects with immediate real-world impact Hands-on involvement in AI, machine learning, and data integration challenges in a scientific environment Close collaboration with a small, highly skilled technical team Ihr Kontakt Referenznummer 863771/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Own, author, record and investigate Deviations across operationsCollaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impactApply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologiesDefine effective CAPAs and associated effectiveness checks to prevent recurrenceEnsure full cGMP compliance throughout the investigation lifecycleDrive quality records to timely and accurate completionSupport continuous improvement activities within operationsContribute to enhancing investigation quality, consistency and efficiencyMaintain strong documentation standards and technical writing qualityCommunicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related fieldExperience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantageKnowledge of biotech manufacturing processes and analytical methods is an advantageExperience with Human and Organizational Performance and risk management approaches is beneficialFluency in English in both written and spoken form; German is an advantageStrong technical writing, analytical and communication skillsStructured, focused and well-organised working styleOpen-minded, agile, highly motivated and adaptable to changeStrong interpersonal and collaboration skills with a proactive mindsetAbility to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environmentExposure to cross-functional teams and complex deviation management processesImpactful role with high visibility in quality and operations functionsInclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
-Ing., or higher)Solid proven project management and leadership experience in mid-sized, complex CapEx projects within the chemical, biotech, or pharmaceutical industryStrong project management skills, including expertise in contract management, cost control, and stakeholder managementDemonstrated experience in process and infrastructure engineering in chemical, biotech, or pharmaceutical environmentsSolid understanding and practical experience with cGxP requirements as well as qualification and validation processesFluent in German and English, both written and spokenProven leadership capabilities with the ability to guide teams and manage departmental responsibilities A highly motivated team and an open way of communication A very renowned companyGood infrastructurePossibilities to work remoteTips on how to prepare a successful application Ihr Kontakt Referenznummer 865168/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Als Engagement Manager – Real World Analytics Germany sind Sie für die Beratung, Entwicklung und Projektbetreuung unserer Kunden aus der pharmazeutischen Industrie verantwortlich.
Use media monitoring and competitor intelligence to identify trends, risks and opportunities, and guide external positioning. Manage proactive and reactive crisis communications issues and serve as contact person during international matters. Lead DACH cluster communications and act as the primary communication partner for regional leadership, ensuring cohesive stakeholder engagement in collaboration with Marburg and Bern manufacturing communication teams.Advise the Tenders & Partnerships and Planning team by shaping public narratives and supporting tender and tolling processes.
Own, author, record and investigate Deviations across operations Collaborate with Subject Matter Experts and key stakeholders to determine root causes and assess product or system impact Apply structured investigational tools such as Fault Tree Analysis, Event & Causal Factors Chart, Fishbone Diagram and similar methodologies Define effective CAPAs and associated effectiveness checks to prevent recurrence Ensure full cGMP compliance throughout the investigation lifecycle Drive quality records to timely and accurate completion Support continuous improvement activities within operations Contribute to enhancing investigation quality, consistency and efficiency Maintain strong documentation standards and technical writing quality Communicate investigation progress and outcomes to relevant stakeholders Bachelor’s degree in chemistry, biotechnology, life sciences or a related field Experience with Deviations and cGMP in a regulated pharmaceutical or API environment is a strong advantage Knowledge of biotech manufacturing processes and analytical methods is an advantage Experience with Human and Organizational Performance and risk management approaches is beneficial Fluency in English in both written and spoken form; German is an advantage Strong technical writing, analytical and communication skills Structured, focused and well-organised working style Open-minded, agile, highly motivated and adaptable to change Strong interpersonal and collaboration skills with a proactive mindset Ability to manage multiple investigations simultaneously in a dynamic environment Opportunity to work in a state-of-the-art large-scale mammalian manufacturing environment Exposure to cross-functional teams and complex deviation management processes Impactful role with high visibility in quality and operations functions Inclusive, international and collaborative workplace culture Ihr Kontakt Referenznummer 863146/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis models Execute full end-to-end in vivo workflows, from study preparation to sample processing and documentation Characterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assays Handle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experiments Perform data analysis, interpret results, and present findings to the research team Maintain accurate, complete, and compliant documentation across all experimental steps Contribute to lab operations, including safety standards, inventory, equipment handling, and general organization Collaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experience Active certification for animal experimentation (e.g., LTK1, FELASA, or equivalent) Proven hands-on experience with rodent work, including intravenous injections and blood sampling Ability to independently design, execute, and manage in vivo studies from start to finish Experience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapy Strong ability to plan experiments, analyze data, and interpret scientific results Fluency in English with clear communication skills Highly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impact Hands-on work with a combination of in vivo, ex vivo, and molecular biology techniques Collaborative environment with close teamwork and modern laboratory infrastructure Diverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
About us Your Contribution Implement and maintain ISO9001 & ISO14001 systems.Plan resources and coordinate QA activities across departments.Lead quality assurance for new product qualifications, including design reviews and inspection plans.Drive process control initiatives (FMEA, SPC monitoring, MSA).Manage incoming and outgoing quality audits and ensure compliance.Perform root cause analysis using 8D methodology and communicate corrective actions to customers.Utilize SAP CRM data and customer feedback for continuous improvement.
About us Your Contribution Ensure throughput and product qualityReview production KPI reports and electronic board for accuracy; control production order variances (hours/material/consumption)Review and manage re-inspection backlogs, quality issues and machine changes, along with handling and material issuesLead, instruct and motivate team employees on department deliverables and objectivesSupervise work performance, perform audits, provide control measures within the range of responsibility, and determine necessary improvement activitiesParticipate in the preparation and modification of job descriptions and the hiring processCreate planning documents and schedule/organize staffing to meet business needs based on the production schedule, vacations, call-offs, special needs, etc.Foster open communication with the Operations Manager, while reporting on all relevant data (production quantities, quality, accomplished order production, tool availability, maintenance tasks, etc.)Host daily shift meetings to provide daily instruction and staff allocationAssist in the development and implementation of training programs, in conjunction with the Department Training Coordinator, while continuously evaluating needs per positionPerform annual performance evaluations; document as requiredIssue disciplinary action for poor performance and/or misconduct, etc.Ensure clean workspaces on the Production floorMaintain the accuracy of employee time and attendance within the payroll systemLead and foster troubleshooting activities regarding potential issues on the Production line(s)Help promote and implement safety/EHS directives and maintain a clean and safe workspaceFollow cGMP and adhere to all ISO and safety guidelines and policies Your Profile High School Diploma or GED, requiredExperience in leading and directing the work of others in a fast paced manufacturing settingExperience in machine operation; glass manufacturing experience highly preferredUnderstanding of ISO and cGMP, preferredAbility to follow directions and instructionsAbility to read, write and speak English languageMulti-tasking abilitiesDetail oriented approachUpbeat, team approachRobust communication skills and openness to learn/develop Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact usYour Profile High School Diploma or GED, requiredExperience in leading and directing the work of others in a fast paced manufacturing settingExperience in machine operation; glass manufacturing experience highly preferredUnderstanding of ISO and cGMP, preferredAbility to follow directions and instructionsAbility to read, write and speak English languageMulti-tasking abilitiesDetail oriented approachUpbeat, team approachRobust communication skills and openness to learn/develop
We know each employee’s individual contributions make us the #1 Delivery and Logistics Company in the world. DHL Global Forwarding manages the flow of goods and information across a customer’s global supply chain utilizing air/ocean/ground transportation, customs brokerage services and dedicated warehousing/distribution centers.
Successful studies in Engineering, Business Administration or Life Sciences (MS/MBA/BS/BA or equivalent) Solid experience in managing major capital projects in the pharmaceutical industry Functional knowledge of cGMPs and manufacturing operations in FDA regulated facility Excellent understanding of project management principles and project lifecycle phases, including knowledge of Validation, CMC and facility regulatory submission requirements Experience to manage high level project budgets Ability to handle many tasks simultaneously and integrate project planning efforts across functions Ability to understand the big picture and approach problem solving in a proactive team manner German knowledge is mandatory Varied work in a renowned companyPleasant working atmosphereSupport throughout the entire application processLook forward to working in an international environment Ihr Kontakt Ansprechpartner Sandro Frei Referenznummer 865163/1 Kontakt aufnehmen E-Mail: sandro.frei@hays.ch Anstellungsart Freiberuflich für ein Projekt
We are strengthening our team and are looking for you for our location in Ispra - Italy. Construction Engineer / Construction Manager in the Dismantling of Nuclear Facilities (m/f/d) Einsatzort: Ispra, Italien Kennziffer: 2025-1316 Arbeitszeit: Vollzeit (unbefristet) Aufgaben Planning of technical projects in the dismantling of nuclear facilities (domestic and international)Preparation of schedules, budget plans and resource plans, including monitoring them for compliance and taking appropriate countermeasures in the event of deviationsLeading the project team and leading project team meetingsExamination of externally prepared planning and application documents, specifications and tender documentsIndependent coordination with planners, surveyors/experts, executing companies and other parties involved in the planningOrganisation and participation in acceptance tests / factory acceptances, detection and intervention in the event of deviations as well as organisation and monitoring of commissioning and cold handlingReporting and participation in work consultations, schedule discussions and other discussions Profil Completed studies in civil engineering or completed training as a state-certified civil engineer. or Construction technician with experience or equivalentStrong technical understandingConfident appearance, negotiation skills, organizational talent and assertivenessSound MS Office skills round off your profileExcellent knowledge of English and Italian desirablePractical experience in construction works, dismantling, or operational nuclear engineering Willingness to travel to the project location in Italy at least once a month Wir bieten A crisis-proof full-time job with a permanent employment contractThe option of hybrid working including Homeoffice Holiday and Christmas bonusExtensive induction by experienced colleaguesA wide range of training and development opportunities in a secure group of companiesEmployee conditions with discounted offers, e.g.: Membership in over 4,500 fitness studios via EGYM Wellpass and job bikeConclusion of an attractive BU (occupational disability insurance) + company pension scheme Have we aroused your interest?
Design, conduct, and analyze in vivo studies involving intravenous injections, blood collection, and bleeding/thrombosis modelsExecute full end-to-end in vivo workflows, from study preparation to sample processing and documentationCharacterize gene therapy candidates using molecular and biochemical assays such as ELISA, thrombin generation, and chromogenic assaysHandle, prepare, and evaluate patient-derived blood and plasma samples for in vitro and ex vivo experimentsPerform data analysis, interpret results, and present findings to the research teamMaintain accurate, complete, and compliant documentation across all experimental stepsContribute to lab operations, including safety standards, inventory, equipment handling, and general organizationCollaborate with cross-functional team members to ensure smooth coordination and progress on gene therapy studies Academic background in life sciences (MSc or BSc) or completed scientific apprenticeship with hands-on laboratory experienceActive certification for animal experimentation (e.g., LTK1, FELASA, or equivalent)Proven hands-on experience with rodent work, including intravenous injections and blood samplingAbility to independently design, execute, and manage in vivo studies from start to finishExperience with molecular or biochemical assays relevant to hemostasis, thrombosis, or gene therapyStrong ability to plan experiments, analyze data, and interpret scientific resultsFluency in English with clear communication skillsHighly organized, proactive, and team-oriented mindset with strong reliability and attention to detail Opportunity to contribute directly to translational gene therapy research with high scientific impactHands-on work with a combination of in vivo, ex vivo, and molecular biology techniquesCollaborative environment with close teamwork and modern laboratory infrastructureDiverse and meaningful daily tasks involving both preclinical models and human biological samples Ihr Kontakt Referenznummer 865654/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
About us Your Contribution Possess knowledge and capabilities to execute Maintenance/Facilities Technician (all levels) roles and responsibilitiesMonitor daily work orders and employee activitiesCoordinate with various department stakeholders on Maintenance actionsHelp minimize machine downtimeLead, coach and train Maintenance TechniciansProcure parts, materials and resources to increase machine uptime; impart expertise and techniques to others within the departmentEstablish shift schedules to meet business needs; manage employee schedulesActively lead and participate in projects/events to drive improvementsFill in for the Maintenance Manager, as neededHelp with achieving department deliverables and initiatives Participate in the interviewing/hiring processHost meetings accordinglyEnsure clean and safe workspacesMaintain attendance within the payroll systemFollow cGMP and adhere to all ISO and safety guidelines and policies Your Profile High School Diploma or GED, required / Vocational school degree, preferredMinimum (3) years of maintenance/facilities experience in leading and directing the work of others in a fast-paced manufacturing settingStrong mechanical aptitudeUnderstanding of ISO and cGMPAbility to foster and follow directions and instructionsAbility to read, write and speak English languageMulti-tasking abilitiesDetail oriented approachUpbeat, team approachService orientedRobust communication skills and openness to learn/developWork a fixes 8-hour shift schedule Monday to Friday, but some weekend/night work, as neededUp to 5% travel, if needed to satisfy business demand Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact us You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future.
About us Your Contribution Perform comprehensive failure analysis using advanced tools and techniques.Analyze complex problems using quality tools and interpret data for actionable insights.Maintain FA tracking lists, equipment logs, and ensure laboratory safety and organization.Interface with process owners to understand key processes and failure mechanisms.Source and manage external laboratories for advanced FA capabilities.Provide clear documentation and publish detailed analysis reports.Participate in cross-functional meetings to communicate findings.Perform data analysis to support root cause investigations and trend monitoring.Support ISO9001, ISO14001, ISO45001 & IATF16949 system implementation.Share technical knowledge to develop team capabilities.
About us Your Contribution Own and control project scopes, schedules and budgets; manage risks/issues and communicate status to stakeholdersLead cross functional execution with Production, Quality, Maintenance, Supply Chain, EHS, and Global EngineeringManage CAPEX, PO releases, FAT/SAT planning, cost tracking/forecasting and accurals; deliver fiscal year plan on time and on budgetPrepare and maintain audit ready documentation aligned to US cGMPOperate in accordance with standard cleanroom conduct consistent with ISO 14644 practices and internal QMS and site Contamination Control StrategyOwn change controls (local and global)- initiaiton, risk assessment, execution plan, verification of effectivensss and closure Lead/support validation and qualification for equipment, products, processes, etc.Integrate into operations; plan trials and downtime, coordinate line readiness/tech transfer, create/update SOPs, define PM requirements and maintenance plans, ensure spares/training are in placeSupport quality investigationsDrive continuous improvement with Lean to improve OEE, scrap rates, uptime and cycle times Mentor/train Engineers and Technicians (no direct reports); structured troubleshooting/problem solving and Best Known Methods; develop quick-reference guides/checklist, where needed Promote safety and EHS and adhere to all Company policies, procedures and guidelines Your Profile Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, Industrial/Manufacturing, Pharmaceutical or Materials) or equivalent4+ years in regulated manfuacturing Project management and CAPEX executionSix Sigma Green/Black Belt and/or PMPValidation and QMS: URS, FMEA, VMP, IQ/OQ/PQ/PV; author/review protocols/reports, managing deviations/CAPA; change controls Working knowledge of cGMP, ISO 9001, ISO 15378Knowledge and experience in leading new equipment/NPI validationsLean/CI; 5S, Kaizen, DMAIC, root cause (5-why, fishbone)Tools: SAP, MS Project, MS TEAMS, Solidworks and MinitabStrong skills in MS Office Ability to read, write and speak EnglishTeam player with upbeat approach Your Benefits Excellent healthcare benefits including medical, dental and visionShort and long term disability Tuition reimbursement Paid time offPet insurance Other supplemental benefits available upon election Please feel free to contact usYour Profile Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, Industrial/Manufacturing, Pharmaceutical or Materials) or equivalent4+ years in regulated manfuacturing Project management and CAPEX executionSix Sigma Green/Black Belt and/or PMPValidation and QMS: URS, FMEA, VMP, IQ/OQ/PQ/PV; author/review protocols/reports, managing deviations/CAPA; change controls Working knowledge of cGMP, ISO 9001, ISO 15378Knowledge and experience in leading new equipment/NPI validationsLean/CI; 5S, Kaizen, DMAIC, root cause (5-why, fishbone)Tools: SAP, MS Project, MS TEAMS, Solidworks and MinitabStrong skills in MS Office Ability to read, write and speak EnglishTeam player with upbeat approach
Für unser Analytics & Consulting Team suchen wir zum nächstmöglichen Zeitpunkt einen erfahrenen Senior Consultant am Standort Frankfurt am Main oder München. Als Engagement Manager übernehmen Sie die Leitung für unsere vielfältigen Beratungsprojekte und sind zentraler Ansprechpartner für unsere wesentlichen internen und externen Stakeholder.
Initiate and formulate proposals / business cases for quality improvement projects including deliverables and planning for the development and implementation of proposed improvements Create and maintain supplier records in the qualification system Assess material changes and drive required quality change controls Support supplier qualification activities and coordinate supplier audits Manage supplier relationships to ensure value delivery and site performance Develop material specifications to support qualification and release Coordinate material release schedules to secure on-time production supply Collaborate with tech transfer, procurement, quality, and manufacturing on supplier and material selection Ensure materials meet required quality grades for clinical manufacturing Align purchase orders and material planning with lead times, safety, quality, cost, and production schedules Support quality investigations, risk assessments, and continuous improvement initiatives including business case development.Bachelor’s or Master’s degree in engineering, pharmacy or science related field or profound experience working in a relevant academic or industry field Renowned pharmaceutical company Long term contract Attractive salary package 25 Days Holiday Ihr Kontakt Referenznummer 863542/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Senior Project Manager KHS is a subsidiary of Salzgitter AG. As one of the world's leading manufacturers of filling and packaging systems for beverages and liquid food we are a world-class player.
You should have: University degree from life science-based subjects preferable plus an advanced theoretical trainings program in clinical research.Excellent communication skills in German language (at least C1 level) including good command of English language.Strong written and verbal communication skills.Computer skills including a high proficiency in use of Microsoft Office applications, especially Excel, internet, and communication tools.Excellent organizational and problem-solving skills.Effective time management skills and the ability to manage priorities.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Flexibility to frequent business travel and driving license category B.Candidates need to be located in Germany If you want to make a difference in global healthcare, IQVIA™ is the place for you!
You should have: University degree from life science-based subjects preferable plus an advanced theoretical trainings program in clinical research.Excellent communication skills in German language (at least C1 level) including good command of English language.Strong written and verbal communication skills.Computer skills including a high proficiency in use of Microsoft Office applications, especially Excel, internet, and communication tools.Excellent organizational and problem-solving skills.Effective time management skills and the ability to manage priorities.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Flexibility to frequent business travel and driving license category B.Candidates need to be located in the Stuttgart area If you want to make a difference in global healthcare, IQVIA™ is the place for you!
Senior Project Manager KHS is a subsidiary of Salzgitter AG. As one of the world's leading manufacturers of filling and packaging systems for beverages and liquid food we are a world-class player.
Develop, maintain and implement the department budget, ensuring cost effective solutions for repairs and upgrade. Manage infrastructure maintenance contracts (negotiation, execution and termination). Manage relationships with external vendors and contractors, ensuring quality service delivery and compliance with contractual terms.
Your Profile BSc/MSC/Ph.D Degree in Mathematics, Computer Science, Information Technology, Physics or Engineering.At least 5 years experience in the field of data analytics, data mining.Technical expert in the field of data analytics, data mining.Proficient in Python and SQL languages.Experienced with statistical modelling and data mining techniques.Strong problem-solving skills with ability to multi-task and manage multiple projects simultaneously. Your Benefits SCHOTT’s openness to promote your further development is just as great as our additional benefits.
We offer talented and motivated individuals the opportunity to grow, develop their skills, and shape their careers with us. Your Role As Site Manager, you are fully responsible for the operational, organizational, and disciplinary leadership at our operational site in Ostrava. You ensure stable operations, high quality standards, and strict compliance with safety, customer, and process requirements.