Charles River Laboratories Switzerland AG sucht in bundesweit, Nord-Europa eine/n Business development and operational Manager – Insourcing Solution (m/f/d) – Germany / Northern Europe (ID-Nummer: 13717186)
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectivesDesign and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regionsBuild and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutionsConduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiativesContribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical dataOversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL DirectorAct as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentationPlan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical OfficerRepresent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencersServe as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic communityCollaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groupsFull professional proficiency in English, both spoken and writtenStrong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflowsExperience with product launches, advisory boards, and post-approval studies is highly advantageousRelevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned companyOther Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Business Development Manager (m/w/d) Healthcare Sensible Supply Chains entwickeln. Märkte gestalten. Verantwortung übernehmen. Healthcare-Logistik bedeutet mehr als Transport sie erfordert Präzision, regulatorisches Verständnis und strategisches Denken.
Für unseren Kunden, ein globales Life-Science-Unternehmen, suchen wir dich zum nächstmöglichem Zeitpunkt in Direktvermittlung Als Key Account Manager (m/w/d) bist du dafür verantwortlich, starke und langfristige Beziehungen zu unseren Kunden aufzubauen und zu pflegen. Du verstehst Patientenpfade und Versorgungsstrukturen, kennst die Bedürfnisse deiner Kunden und sorgst dafür, dass sie effektiv bedient werden, um neben einer hohen Kundenzufriedenheit sowohl das Ansehen des Unternehmen als ein zuverlässiger Partner in der Onkologie als auch die Erfüllung der Umsatzziele zu erreichen.
Für unseren Kunden, ein globales Life-Science-Unternehmen, suchen wir dich zum nächstmöglichem Zeitpunkt in Direktvermittlung Als Key Account Manager (m/w/d) bist du dafür verantwortlich, starke und langfristige Beziehungen zu unseren Kunden aufzubauen und zu pflegen. Du verstehst Patientenpfade und Versorgungsstrukturen, kennst die Bedürfnisse deiner Kunden und sorgst dafür, dass sie effektiv bedient werden, um neben einer hohen Kundenzufriedenheit sowohl das Ansehen des Unternehmen als ein zuverlässiger Partner in der Onkologie als auch die Erfüllung der Umsatzziele zu erreichen.
Eppendorf SE sucht in eine/n Senior Manager/Projektleiter Construction Management (m/w/d) (ID-Nummer: 13504269)
Elis Deutschland sucht in eine/n Key Account Manager Vertrieb Cleanroom (m/w/d) Region: Bayern (ID-Nummer: 13665475)
Ensure high-quality, data-driven deliverables that meet the highest standards of medical, ethical, and scientific integrity and conduct. Propose strategies to manage and accelerate timelines for drug development strategies. Identify, promote, and develop innovation in pharmaceutical product development.
Develop and execute strategies to enhance advocacy and engagement among key eye-care providers, ensuring alignment with overall brand and commercial objectives Design and implement training approaches that enable local SSCs to identify, recruit, and cultivate strong relationships with KOLs within their regions Build and sustain robust relationships with the ophthalmic medical community- including academic institutions and specialized physicians-using a scientific, needs-based approach to deliver targeted solutions Conduct an annual needs assessment for KOL activities and create regional execution plans in collaboration with key internal stakeholders; provide leadership with ongoing progress updates on the impact of regional KOL initiatives Contribute to the development of advanced communication programs to ensure KOLs receive timely updates on company developments, products, and clinical data Oversee and maintain the regional KOL database to ensure accuracy, completeness, and effective engagement tracking through honoraria; annually update contracted HCP biographies and publications, ensuring all documentation remains current; deliver periodic utilization and budget reports to the Global KOL Director Act as the primary liaison with the legal department to develop and manage KOL contracts and service agreements in full compliance with regulatory requirements; coordinate and process all onboarding documentation Plan, coordinate, and execute approved regional advisory boards in support of KOL Management and the Chief Medical Officer Represent the company at regional medical congresses and scientific meetings, supporting KOL strategy execution and identifying emerging key influencers Serve as an internal expert on disease state and product knowledge, empowering internal and field teams to better understand clinical needs, strengthen KOL loyalty, and foster broader adoption within the ophthalmic community Collaborate closely with internal teams-including Marketing, R&D, and Professional Education—to address cross-functional KOL needs and ensure smooth coordination of activities Solid direct experience working with Key Opinion Leaders, ideally within the ophthalmology sector Exceptional communication and interpersonal skills, with the ability to build trust-based relationships across diverse stakeholder groups Full professional proficiency in English, both spoken and written Strong business acumen and a demonstrated ability to effectively manage timelines, processes, and procedural workflows Experience with product launches, advisory boards, and post-approval studies is highly advantageous Relevant academic background required (e.g., life sciences, healthcare, business, or a related field) A very renowned company Other Locations: Oberkochen/Jena/Berlin Ihr Kontakt Referenznummer 865508/1 Kontakt aufnehmen Telefon:+ 49 621 1788-4297 E-Mail: positionen@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
About us Your Contribution Service & Support Manage incidents and changes via ITIL processes (ServiceNow).Provide 2nd-level support for key users and application users.Deploy bug fixes, configuration changes, and minor enhancements.Support rollout activities at new factories.Gather requirements and user feedback for consulting team.
We are looking in Portugal country for a IT Local Manager to: WMS solution expert for implementation of migration projects Leads solution design and WMS configuration according with business requirements and ensure smooth implementation Analyze and perform functional requirements for new functionalities and Integration process with client and other applications.
In Deinem Job: übernimmst du die Verantwortung für die Zufriedenheit unserer Bestandskunden in den Industrien Prozessfertigung, Life Science und Chemical. arbeitest du eng mit den Account Managern zusammen und baust eine nachhaltige Vertrauensbasis zu unseren Kunden auf. gehst du aktiv in den Austausch mit Kunden und unterstützt dein Team, verschiedene Kundensituationen bestmöglich zu bedienen und positiv zu verändern.
What makes you stand out You hold a degree in Business Informatics, Data Science, Computer Science, Industrial Engineering, Business Administration, or a comparable field.You bring experience in Revenue Operations, Sales Operations, Sales Analytics, or a similar commercial analytics role.You have a strong understanding of sales processes, pipeline management, forecasting, and revenue metrics, and you can translate them into technical requirements for engineers.You hold a degree in Business Informatics, Data Science, Computer Science, Industrial Engineering, Business Administration, or a comparable field.You are a great stakeholder manager who can talk to sales and engineering alike.You are highly proficient in Power BI and experienced in building dashboards that drive action.You are comfortable working with CRM data and sales systems (e.g.
Eppendorf SE sucht in eine/n Senior Manager Global Master Data (m/w/d) (ID-Nummer: 13664042)
KG sucht in eine/n Vertriebssachbearbeiter Export / Channel Partner Manager/ (m/w/d) (ID-Nummer: 13594158)
BIOZOL Diagnostica Vertrieb GmbH sucht in Hamburg eine/n Kaufmännischer Mitarbeiter als Office Manager (m/w/d) (ID-Nummer: 13162368)
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
IAB Reinraum-Produkte GmbH sucht in Braunschweig eine/n International Sales Manager / Vertriebsinnendienstmitarbeiter (m/w/d) (ID-Nummer: 13677876)
In light of this spirit, SCHOTT Pharma is committed to sustainable development for society and the environment. We are seeking an experienced Area Sales Manager to lead sales growth of our SCHOTT Pharma portfolio in eastern Europe. You develop customer-specific solutions, drive growth, build strong partnerships, and act as a key interface between customers and internal stakeholders.
Macromedia University sucht in eine/n Lecturer Manager (m/w/d) (ID-Nummer: 13764302)
Integration Specialist (m/w/d) am Standort Erlangen >> Stundenlohn: ab 33,00 € + Zuschläge >> Sehr hohe Übernahmeoption >> Einsatzort: Erlangen Deine Aufgaben als Integration Specialist (m/w/d) am Standort Erlangen Responsibilities: Support migration activities from one cloud provider to another (GCP to Azure) Integrate and maintain software solutions within an Azure environment. Set up and manage CI/CD pipelines and repositories. Ensure code quality and sustainability, following prescribed style guides and software patterns.
Integration Specialist (m/w/d) am Standort Erlangen >> Stundenlohn: ab 33,00 € + Zuschläge >> Sehr hohe Übernahmeoption >> Einsatzort: Erlangen Deine Aufgaben als Integration Specialist (m/w/d) am Standort Erlangen Responsibilities: Support migration activities from one cloud provider to another (GCP to Azure) Integrate and maintain software solutions within an Azure environment. Set up and manage CI/CD pipelines and repositories. Ensure code quality and sustainability, following prescribed style guides and software patterns.
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
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
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
What you can expect You take on the functional and disciplinary responsibility for all FTEs in the Sales Data Hub within the federated data setup, including Data Engineers, Data Scientists, Data Governance roles and Product Owners Data.You define, design, develop, and operate cloud‑based data products for the Sales, Marketing, and Customer Service business units.You are responsible for the methodological integration of data assets and data products.You manage the Sales Data Hub operationally and further develop it as a specialized unit for data‑driven solutions in Sales, Marketing, and Customer Service.You are responsible for the further development and ongoing maintenance of all sales‑related models based on feedback and requirements from the sales organization.You lead projects related to planning, expanding, and organizing new and existing products in collaboration with the relevant business units and external partners.You assume technical responsibility for data products developed by or for the Sales, Marketing, and Customer Service areas within the Data Intelligence & Analytics team.You drive the continuous expansion, professionalization, and organizational development of the Sales Data Hub within the existing governance and organizational framework.
FERCHAU – Connecting People and Technologies sucht in Ulm eine/n Clinical Trial Manager (m/w/d) (ID-Nummer: 13490969)
Wir freuen uns auf Ihre Bewerbung! 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.
Eppendorf SE sucht in eine/n Senior Project Manager IT (ID-Nummer: 13523567)
Das macht uns aus Familiäre Atmosphäre im internationalen UnternehmenHerausfordernde Tätigkeiten in einem professionellen UmfeldGute Entwicklungsmöglichkeiten durch kontinuierliches Wachstum der UnternehmensgruppeSichere ArbeitsplätzeLeistungsorientierte VergütungFlexible ArbeitszeitgestaltungUmfangreiche Schulungsmaßnahmen YouTube-Video ansehen Ihr Ansprechpartner OPTIMA packaging group GmbH Tina Nassen HR Manager Personnel Acquisition Mail: tina.nassen@optima-packaging.com Tel.: +49 151 54686991 Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre Online-Bewerbung Stellenangebot teilen über Wichtiger Hinweis zu Ihrer Bewerbung: Bitte bewerben Sie sich ausschließlich in digitaler Form über unsere Karriereseite auf unsere ausgeschriebene Stelle.
Gemeinsam tun wir alles dafür, dass unser Team auch in Zukunft Optima, das Beste ist. #wecareforpeople. Als Technical Support Manager (m/w/d) sind Sie Teil von Optima Pharma Containment und wirken bei der Entwicklung maßgeschneiderter Isolatoren und weiteren Reinraumtechnologien mit.
Bund-Verlag GmbH sucht in eine/n Operativer Data Manager (m/w/d) (ID-Nummer: 13724653)
Bertin GmbH sucht in eine/n (Junior) Project Manager (m/w/d) (ID-Nummer: 13715788)
FERCHAU – Connecting People and Technologies sucht in Marburg eine/n Senior Account Manager Pharma (m/w/d) (ID-Nummer: 13343864)
Manager Public Affairs (m/w/d) 1047 Brussels Bruxelles Belgium Marketing & Communications Berufseinsteiger / Berufserfahrene Vollzeit Berufseinsteiger / Berufserfahrene About us The ALDI Nord group is one of the leading food retailers.
Solventum GmbH sucht in eine/n Manager Technology Platforms (m/f/x)* – Dental Materials (ID-Nummer: 13724913)
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
Das Leistungsspektrum reicht von der Anlagen-Optimierung bis zur Generalplanung von Großinvestitionen. Zur Verstärkung unseres Teams suchen wir Dich als Construction Manager (m/w/d). Dich erwarten spannende Projekte, viel Gestaltungsspielraum und ein motiviertes Team mit exzellentem Arbeitsklima. Unsere Besonderheiten: Flexible Arbeitszeitgestaltung (Gleitzeit ohne Kernarbeitszeit)Mobiles ArbeitenGroßzügige Regelungen bei Reisezeit und ÜberstundenModerne Arbeitsausrüstung (Laptop, Smartphone)Flache Hierarchien und Duz-KulturEngagiertes und dynamisches Team mit hervorragendem ArbeitsklimaFreiraum für EigeninitiativeModerne Büroräumlichkeiten mit gut ausgestatteten Sozialräumen/KüchenDiverse Mitarbeiter- und TeameventsFamilienfreundliches Unternehmen mit vielfältigen Förderungen zur Vereinbarkeit von Beruf, Familie und Privatem über alle Lebensphasen Das sind Deine Aufgaben: Überwachung, Koordination und Organisation aller Bauarbeiten gemäß vertraglichen Verpflichtungen in allen ProjektphasenEinsatz überwiegend auf Baustellen beim Kunden vor Ort in der D/A/CH-RegionBauablaufplanung sowie Kostenschätzung und StundenkalkulationTerminplanung, -steuerung und -überwachungAbstimmung und Schnittstellenkoordination mit allen beteiligten GewerkenFührung des Bautagebuchs und Organisation von BesprechungenSicherstellung und Umsetzung der Sicherheitsrichtlinien auf der Baustellen Das bringst Du mit: Abgeschlossene Berufsausbildung sowie Meister, Techniker oder eine vergleichbare QualifikationMehrjährige Erfahrung in der Abwicklung von Großprojekten im Anlagenbau, idealerweise in der Pharma- oder verfahrenstechnischen IndustrieErfahrungen im ProjektmanagementSehr hohe Reisebereitschaft innerhalb der D/A/CH-Region (bzw. innerhalb der Länder der VTU-Gruppe)Kommunikationsstärke, Konfliktfähigkeit und DurchsetzungsvermögenEigenverantwortliche Arbeitsweise und BelastbarkeitFreude an der Zusammenarbeit mit Leuten verschiedener FachrichtungenSehr gute Deutschkenntnisse und Englischkenntnisse Weitere Extras für Dich: 30 Tage UrlaubIndividuelle Weiterbildungsmöglichkeiten (Karriere-Pyramide, VTU-Academy)Aktive Gesundheitsförderung (z.
Gerne auch wenn Sie sich unsicher sind, ob Sie alle Anforderungen erfüllen - wir stimmen die für Sie passende Aufgabenverteilung gemeinsam ab. Ihr Ansprechpartner: Adrian Bazzini HR Manager Tel: +49 (0)89 641 808 - 0
Das machen Sie bei uns Programmierung und Inbetriebnahme von pharmazeutischen Abfüllanlagen und Robotik Systemen ausgestattet mit Steuerungskomponenten der Firmen Siemens, Rockwell, B&R oder BeckhoffMitarbeit bei der Weiterentwicklung unseres plattformübergreifenden Softwarestandards und Integration der Entwicklungsergebnisse in unsere pharmazeutischen AnlagenDirekte Zusammenarbeit mit den Entwicklungsbereichen Software Design und mechanische KonstruktionEntwicklung von Software Modulen zur Bahnplanung an kinematischen SystemenTechnische Abklärung mit KundenUmsetzung von Kunden- und ProzessspezifikationenBetreuung der Maschine bis hin zur Abnahme beim Kunden Damit bereichern Sie unser Team Abgeschlossenes Hochschulstudium oder Weiterbildung zum Techniker in den Fachrichtungen Elektrotechnik, Mechatronik oder RobotikMehrjährige Programmiererfahrung in den Gebieten Motion Control und SPSErste Erfahrungen in der Programmierung von Robotik SystemenAbteilungsübergreifende interdisziplinäre Denkweise Hohes Maß an Eigeninitiative, Zielorientierung und selbstständiger ArbeitsweiseAusgeprägtes analytisches und abstraktes DenkvermögenTeamplayer sowie offen für Neues Gute Englischkenntnisse in Wort und SchriftGelegentliche Reisebereitschaft Das macht uns aus Familiäre Atmosphäre im internationalen UnternehmenHerausfordernde Tätigkeiten in einem professionellen UmfeldGute Entwicklungsmöglichkeiten durch kontinuierliches Wachstum der UnternehmensgruppeSichere ArbeitsplätzeLeistungsorientierte VergütungFlexible ArbeitszeitenUmfangreiche Schulungsmaßnahmen YouTube-Video ansehen Ihr Ansprechpartner OPTIMA packaging group GmbH Tina Nassen HR Manager Personnel Acquisition Mail: tina.nassen@optima-packaging.com Tel.: +49 151 54686991 Haben wir Ihr Interesse geweckt? Dann freuen wir uns auf Ihre Online-Bewerbung Stellenangebot teilen über Wichtiger Hinweis zu Ihrer Bewerbung: Bitte bewerben Sie sich ausschließlich in digitaler Form über unsere Karriereseite auf unsere ausgeschriebene Stelle.
Agile Heroes GmbH sucht in eine/n KI-Manager & Trainer (m/w/d) (ID-Nummer: 13353751)
adp MERKUR GmbH sucht in eine/n Data Manager (m/w/d) (ID-Nummer: 13664560)
Participate in research projects as needed. Communication: Attend lab/clinic meetings as directed by Lab Manager. Ensure effective communication with other departments and TFP. Participate in patient information events and represent TFP at industry conferences.
Sunrise Medical GmbH sucht in eine/n Brand Manager Mobility (w/m/d) (ID-Nummer: 13762090)
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
Löwenstein Medical SE & Co. KG sucht in eine/n Internationaler Marketing Manager (m/w/d) (ID-Nummer: 13753292)
Löwenstein Medical SE & Co. KG sucht in eine/n Manager internationale Messeorganisation (m/w/d) (ID-Nummer: 13753318)
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n IT Operations Manager (m/w/d) (ID-Nummer: 13723269)
We currently offer the exciting opportunity to join the team as Clinical Trial Manager (m/w/d) in full-time and work home-based throughout Germany. In this role you will be accountable for the operational management of the component of clinical trials.
Löwenstein Medical SE & Co. KG sucht in eine/n Manager Schulungen und Seminare in der Löwenstein-Academy (m/w/d) (ID-Nummer: 13753236)