Your Tasks & Responsibilities: Brand Strategy & Execution Develop and implement data‑driven, multi‑channel marketing strategies for vaccine brandsDesign marketing initiatives based on market dynamics, competition, and customer insightsOptimize the customer journey by ensuring relevant and seamless interactions across all touchpointsStrengthen the Sales Journey by leveraging CRM data for preparation, enhancing iPad-supported conversations, enabling consent generation, and driving follow-up through approved emailAnalyze trends, customer behaviors, and performance metrics to refine brand positioning and strategic decision-makingEnsure brand consistency and targeted, impactful messaging across all channels Cross-Functional Collaboration & Digital Innovation Align brand and digital strategies with Sales, Medical, Market Access, Operations, and other key partnersUse CRM systems, marketing automation, and analytics to optimize engagement and overall performanceChampion digital adoption and innovative solutions, particularly within the field forceSupport the organization in expanding digital expertise and fostering a continuous improvement mindset Compliance & Performance Monitoring Track and evaluate marketing initiatives to measure effectiveness and optimize future strategiesEnsure compliance with relevant regulations (e.g., HWG, AMG, industry codes) and internal quality standards Your Skills and Experience University degree in Business, Science, IT, or a related field3–5 years of experience in brand management or digital marketing within the pharmaceutical/healthcare industryStrong knowledge of multi‑channel marketing, CRM, and data‑driven engagement strategiesExperience collaborating with cross-functional teams and influencing key stakeholdersA digital-first mindset with a passion for innovation, analytics, and continuous improvement What We Offer A meaningful role contributing to public health by supporting vaccine awareness and accessibilityThe opportunity to shape digital transformation and drive innovative customer engagement strategiesA collaborative, inclusive environment with strong cross‑functional partnershipsProfessional development opportunities, including digital marketing upskilling and leadership exposureGreat compensation package and benefits such as a pension scheme, including flexible working arrangementsA culture that values curiosity, continuous learning, and a forward‑thinking mindset About CSL Seqirus CSL Seqirus is part of CSL.
About us Your Contribution Develop and progress into a technical expert for specialty vials and ready-to-use [RTU] vials, supporting growth with our innovative productsCollaborate within a global, cross-functional team (sales, product management, quality, pharma services)Design and execute targeted roadshows with market intelligence, sales, and marketing in biotech hubs across the United States Act as a technical expert to introduce high-value products to the biotech sectorIdentify and acquire new customers; support cross-selling of high-value products to established accountsUnderstand the drug formulation for clients, along with their challenges, while providing technical solutionsFollowing all Company policies, procedures, along with Code of Conduct and safety guidelines Your Profile Bachelor’s Degree in natural science (Chemistry, Physics, Biology, Pharmacy, Biotechnology) or EngineeringAt least 3 years of experience in business development or related roles in a B2B environment within an international organizationExperience in pharmaceutical packaging, medical devices, or biotechnology, strongly preferredProven project management, analytical, and conceptual skillsFluent in English (additional languages are a plus)Willingness to travel up to 60%Strong analytical skillsDemonstrated project management skill, along with conceptual skillsWell-organized and highly motivated 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.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Mein Arbeitgeber Ein international tätiger Hersteller radiopharmazeutischer Produkte mit Hauptsitz in SachsenDas Unternehmen ist global führend in der Entwicklung von PET/SPECT-Precursoren, Reagent Kits, sterilen Injectables und GMP-zertifizierten Radiopharmaka – inklusive eigenständiger kompletter Wertschöpfungskette vom Precursor bis zum fertigen Arzneimittel Entwicklung und Umsetzung von Market-Access-Strategien für radiopharmazeutische Produkte (inkl. neuer PET/SPECT-Tracer)Erstellung und Pflege von Value Dossiers, AMNOG-Unterlagen, Nutzenargumentationen und HTA-DokumentenPricing-Strategien für Spezialpräparate, Diagnostika und sterile InjectablesAnsprechpartner für Kostenträger, G-BA, Krankenkassen, Klinik-Einkauf, Nuklearmedizinische Zentren Enge Zusammenarbeit mit medizinisch-wissenschaftlichen Key Stakeholdern (Nuklearmediziner, Radiologen, onkologische Zentren)Unterstützung des Außendienstes bei Erstattungs- und VersorgungsfragenUnterstützung bei der Implementierung neuer Indikationen in Kliniken und ZentrenZusammenarbeit mit Regulatory Affairs für Zulassungs- und ErstattungsprozesseBegleitung klinischer Projekte und Studien, wenn diese Market-Access-Relevanz besitzenSchnittstellenarbeit zu Medical Affairs, Vertrieb, Produktmanagement Erfahrung im Market Access, idealerweise im Bereich Onkologie, Nuklearmedizin, Radiopharmazeutika, Diagnostik oder Specialty PharmaceuticalsFundiertes Verständnis von AMNOG-Prozessen, HTA-Anforderungen und ErstattungslogikenErfahrung im Umgang mit klinischen Daten, Nutzenbewertungen und Pricing-ModellenVorteilhaft: Kenntnisse steriler/aseptischer Produktion oder Radiopharmazie (PET/SPECT)Strategisch denkend und gleichzeitig umsetzungsstarkKommunikationsstark, überzeugend, sicher im Stakeholder-HandlingHohe analytische Kompetenz und strukturierte ArbeitsweiseProaktiv, selbstständig und organisationsstark Arbeit mit hochinnovativen Produkten an der Spitze der NuklearmedizinInternationales, wissenschaftlich geprägtes UmfeldMöglichkeit, echten Impact im Gesundheitswesen zu schaffen (Diagnostikzugang, onkologische Versorgung)Professionelles Team, moderne Arbeitsbedingungen und attraktive Vergütung Gehaltsinformationen Attraktive SozialleistungenAttraktive, leistungsorientierte Vergütung Ihr Kontakt Ansprechpartner Tobias Fleßner Referenznummer 864906/1 Kontakt aufnehmen E-Mail: tobias.flessner@hays.de Anstellungsart Festanstellung durch unseren Kunden
Sunrise Medical GmbH sucht in eine/n Brand Manager Mobility (w/m/d) (ID-Nummer: 13762090)
Löwenstein Medical SE & Co. KG sucht in eine/n Restaurant Manager / Restaurantleitung (m/w/d) (ID-Nummer: 13752685)
Löwenstein Medical SE & Co. KG sucht in eine/n Manager internationale Messeorganisation (m/w/d) (ID-Nummer: 13753318)
With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers.
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n IT Operations Manager (m/w/d) (ID-Nummer: 13723269)
We offer a competitive compensation package (Relocation Assistance, Medical, Dental, Vision, Vacation, Sick, Holiday Pay, 401k, Paternal and Maternal leave, relocation assistance, short-term and long-term disability and more) LEYBOLD USA INC. is an Equal Opportunity Employer – M/F/Disabled/Veterans #LI-Remote #UUY Job location This remote role involves frequent travel—about 50%—including overnight and multi-day domestic and international trips.
DHL offer its employees a good starting rate along with a full benefits package that includes medical, dental and vision insurance along with 401k and tuition assistance. DHL is an equal opportunity employer. We evaluate qualified applicants without regard to race, sex, color, religion, sex, national origin, disability, veteran status and other protected characteristics.
In addition, DHL offers the following: ·Paid time off: Holiday, Float Holiday, Vacation, and Sick ·Medical, Prescription, Dental, and Vision plans ·401K plan with a match ·Employee Discount plan ·Tuition Assistance Plan As the world’s leading logistics’ company, DHL offers a wide range of interesting job challenges and opportunities in our different divisions around the globe.
Dabei stellst du sicher, dass diese wissenschaftlich überprüft und angemessen referenziert werden, von hoher Qualität sind sowie den einschlägigen Verfahren des Unternehmens, des Medical Office und der lokalen Behörden entsprechen. Übernimm Verantwortung! Du verantwortest die Projektleitung in und zwischen den Teams vor Ort und im therapeutischen Bereich, einschließlich angemessener Zuweisung und Überwachung des lokalen MSL-Budgets.
Die Unterstützung bei der Erstellung relevanter SOPs rundet dein Aufgabengebiet ab. dein profil: Erste Berufserfahrung als Medical Science Liaison Manager ist zwingende Voraussetzung. Zusätzlich von Vorteil wäre eine Promotion oder postgraduale Qualifikation.
Sie sind verantwortlich für die Entwicklung und Umsetzung lokaler medizinischer Taktiken für CRSwNP unter Berücksichtigung globaler Ziele und lokaler GegebenheitenSie sind Ansprechpartner für funktionsübergreifende Teams, erstellen integrierte Brand-Pläne Sie planen und führen medizinische Aktivitäten wie Advisory Boards, wissenschaftlicher Präsentationen und Kongressauftritte durchSie unterstützen bei der Erstellung von Werbe- und Schulungsmaterialien unter Einhaltung regulatorischer VorgabenSie sind verantwortlich für die Identifizierung lokaler Datenlücken und proaktive Initiierung von Evidence-Generation-Projekten Abgeschlossenes Hochschulstudium in Medizin, Pharmazie oder Naturwissenschaften (z. B. MD, PhD, PharmD)Relevante Erfahrung im Bereich Medical Affairs in der pharmazeutischen Industrie, idealerweise im Bereich Atemwegs- oder chronisch-entzündlicher ErkrankungenSie bringen ausgeprägte Fähigkeit, komplexe wissenschaftliche Daten in zielgruppengerechte Kommunikation zu übersetzen mitSie haben profunde Kenntnisse des deutschen Gesundheitssystems, des Market-Access-Umfelds sowie in der Generierung von Real-World-EvidenceSie haben sehr gute Deutsch- und Englischkenntnisse und bringen die Bereitschaft zu Reisen innerhalb Deutschlands mit Abwechslungsreiche Tätigkeit in einem renommierten UnternehmenBetreuung im gesamten BewerbungsprozessBetreuung im laufenden Projekt durch unser TeamEngagiertes, innovatives, freundliches Team Ihr Kontakt Ansprechpartner Susann Otto Referenznummer 862928/1 Kontakt aufnehmen E-Mail: susann.otto@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Heraeus Medical GmbH sucht in eine/n Risk Manager Medical Device (m/w/d) (ID-Nummer: 13573326)
BEC Medical GmbH sucht in eine/n Innovativer Qualitätsmanager / Regulatory Affairs Manager Medizinprodukte (Mensch) (ID-Nummer: 13669004)
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n Business Applications Manager DMS (m/w/d) (ID-Nummer: 13723268)
Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.
WHAT YOU WILL DO Interactions primarily involve presenting to or influencing business representatives or vendors Interact primarily in issues related to specific phases of work or technical issues Participate in project meetings to argue for the test relevancy Specify logical and physical test cases, starting scenarios and test scripts Set up and maintain test environments Evaluate automation potential and define setup for automation and analyze the requirement complexity and estimate the test effort Conduct test analysis and design Execute manual and automated test cases (dynamic testing) and check and assess test results and manage defects Provide expert advice, training and technical assistance Contribute to employees’ professional development WHAT YOU SHOULD HAVE 5-8 years of experience including 3+ years of testing with emphasis on analysis and problem solving skills Experience in software development, service management Experience in test script development Strong in testing (test analysis & design, test execution, defect management process) and test management Strong in VB/Java scripting development (for test automation) Good knowledge of automation framework design Strong conceptual thinking and sense of responsibility Solid in business communications and business focus (service, relationship and quality) Solid business communications knowledge State-of-the-art knowledge of test related technologies, processes, and practices WHAT IS THE PLUS POINT(S) Strong technical skill of Vb scripting or Java programming Good understanding of test automation framework and/or open source tool set Hands on web services / API testing also integration with Jenkins, GitHub and any ALM tool WHAT YOU WILL GET FROM US Great Team of IT Professionals with Global Working Exposure Meal Card and Flexible Benefits – Customized According to Individual Needs On-Going Professional and Technical Training and Certifications A Multicultural Environment in Modern Offices Choose Any Day for Your Vacation From Earned Public Holiday (Saturday and Ad Hoc) Smart Casual Everyday Global Internal Job Opportunities Available Within DPDHL Unlimited Outpatient Medical Home Office Possibilities Sounds good? Start your application now! DHL IT Services – About Us IT Services is the internal provider of specialized IT Build services and industrialized IT Run services to Deutsche Post DHL (DPDHL) Group: Supports over 260,000 DPDHL e-mail users;Runs more than 7700 servers;Supports more than 2000 global services and applications;Processes 9 million shipment information messages per day;200000 man days per year of development application.
AstraZeneca sucht in eine/n Medical Affairs Manager Oncology (Lung Cancer) (m/w/d) (ID-Nummer: 13722966)
CompuGroup Medical Deutschland AG sucht in eine/n (Junior) Sales Manager Apotheke (m/w/d) [JR107567] (ID-Nummer: 13576029)
CompuGroup Medical Deutschland AG sucht in eine/n Product Sales Manager Apotheke (m/w/d) [JR107828] (ID-Nummer: 13576035)
Löwenstein Medical SE & Co. KG sucht in eine/n Manager Schulungen und Seminare in der Löwenstein-Academy (m/w/d) (ID-Nummer: 13753236)
Add on:- Dash boarding(Mashzone or Presto) added advantage SAG Product administration (Linux) added advantage WHAT YOU WILL GET FROM US Great Team of IT Professionals with Global Working Exposure Meal Card and Flexible Benefits – Customized According to Individual Needs On-Going Professional and Technical Training and Certifications A Multicultural Environment in Modern Offices Choose Any Day for Your Vacation From Earned Public Holiday (Saturday and Ad Hoc) Smart Casual Everyday Global Internal Job Opportunities Available Within DPDHL Unlimited Outpatient Medical Home Office Possibilities Sounds good? Start your application now! DHL IT Services – About Us IT Services is the internal provider of specialized IT Build services and industrialized IT Run services to Deutsche Post DHL (DPDHL) Group: Supports over 260,000 DPDHL e-mail users;Runs more than 7700 servers;Supports more than 2000 global services and applications;Processes 9 million shipment information messages per day;200000 man days per year of development application.
Blickling sucht in München eine/n CMC Manager – Biopharmazeutische Proteine in einem Medical Device (m/w/d) – Projektleitung & CDMO Management (ID-Nummer: 13746943)
Medical Training & Education Manager TAVI (m/w/d) in Frankfurt am Main Sie arbeiten als Leiter der internen Trainingsabteilung (m/w/d) für ein renommiertes, international stark wachsendes Unternehmen, das als Marktführer in der Kardiologie etabliert ist.
HR Manager Germany (m/w/d) - Medical Device in Frankfurt am Main Sie arbeiten als HR Manager Germany (m/w/d) für ein renommiertes, international stark wachsendes Unternehmen, das als Marktführer in der Kardiologie etabliert ist.
Für den Bereich Spezialpharmazeutika suchen wir dich zum schnellstmöglichen Zeitpunkt als Medical Science Liaison (w/m/d) für den Bereich Onkologie in Direktvermittlung. deine aufgaben: Networking ist alles! Du baust belastbare Beziehungen zu Experten, Entscheidern und Verbänden im medizinisch-wissenschaftlichen Bereich aus.
Zu guter Letzt erstellst du strategische Handlungsempfehlungen für Medical Affairs. dein profil: Du besitzt ein erfolgreich abgeschlossenes medizinisches oder naturwissenschaftliches Studium? Du hast bereits Erfahrung als Medical Science Liaison Manager im Bereich Onkologie?
What we offer Work in an international company with an established position on the market.High standard of work in an international corporation.Opportunities for professional and personal development.Employment based on an employment contract.A package of non-wage benefits, including medical care, Multisport cards, learning English or German.Tools necessary for work (laptop, phone, company car). We are looking forward to your application and to applicants who enrich our diverse culture!
regenold GmbH sucht in eine/n Regulatory Affairs Manager (m/f/d) in-vitro diagnostic medical devices / CDx I 80-100% (ID-Nummer: 13764773)
Leitung Geschäftsfeld Senioren-WG (m/w/d) medcareer Ihre Personalvermittlung für Medical & Healthcare sucht im Auftrag eines innovativen Pflegeanbieters eine unternehmerisch denkende Führungspersönlichkeit für den Aufbau und die Leitung neuer Senioren-Wohngemeinschaften im Rheinland.
We know: motivated and committed employees are the precondition for the success of our company. Further training and education; Free Parking; Medical, Dental and Vision coverage; Talent development; Team Events; paid vacation days, holidays and sick time 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.
We offer a competitive compensation package (Relocation Assistance, Medical, Dental, Vision, Vacation, Sick, Holiday Pay, 401k, Paternal and Maternal leave, relocation assistance, short-term and long-term disability and more) Compensation: The starting salary for this role differs based on the employee's primary work location.
"Ihre" Stelle ist eine Erstbesetzung im Sinne eines Business-Developments.Erfolgreich abgeschlossenes Studium im Bereich Humanmedizin, Pharma oder auch angewandte Biochemie sowie Biotechnologie Eine erfolgreich abgeschlossene Management-Qualifizierung, idealer Weise mit MBA-Abschluss Mehr als 5 Jahre Berufserfahrung im Bereich Medical Nutrition (Ernährungsmedizin) bzw. angewandte Pharmazie Expertise im Bereich klinischer Studien und Anwendungsstudien German language required: C1 Level and English business language: C1 LevelAußertariflichen Anstellungsvertrag in einer Europa-Holding Unternehmerischer Freiraum aber auch Gestaltungsverantwortung Eine einmalige Business Development/ Start-Up Chance Management-Aufgabe in einem weltweit anerkannten und führenden Unternehmen für Ernährungs- und Nahrungsmittel-InnovationenAls Personalberater sind wir exklusiv mit der Betreuung dieses Stellenangebotes beauftragt.
Examples : Windows NT, MVS, Unix, LinuxExperiences in supporting data storage ( Oracle, SQI, Informix), ISQL data extractionEDI Integration solutions – development and implementation experiences in electronic data exchange with our trading partners and DHL applications and information management systems.Configuration Management and coordinate the end-to-end integration testing.Familiar with DHL ITS Build solution delivery process.Project management, Biz System Analysis, and B2B EDI solution development and implementation.DCG technical consultancy and design end-to-end integration B2B and EDI solutionExtend 3rd level production supports for DCG EDI customer solutions deployed globallyWilling to work on shifts.( AP, EU, US) WHAT YOU WILL GET FROM US Great Team of IT Professionals with Global Working Exposure Meal Card and Flexible Benefits – Customized According to Individual Needs On-Going Professional and Technical Training and Certifications A Multicultural Environment in Modern Offices Choose Any Day for Your Vacation From Earned Public Holiday (Saturday and Ad Hoc) Smart Casual Everyday Global Internal Job Opportunities Available Within DPDHL Unlimited Outpatient Medical Home Office Possibilities Sounds good? Start your application now! DHL IT Services – AboutUs IT Services is the internal provider of specialized IT Build services and industrialized IT Run services to Deutsche Post DHL (DPDHL) Group: Supports over 260,000 DPDHL e-mail users;Runs more than 7700 servers;Supports more than 2000 global services and applications;Processes 9 million shipment information messages per day;200000 man days per year of development application.
Medical Affairs Manager (m/w/d) – Kardiologie – Wohnort bundesweit in Frankfurt am Main Sie arbeiten als Medical Affairs Manager (m/w/d) für ein renommiertes, international stark wachsendes Unternehmen, das als Marktführer in der Medizintechnik etabliert ist.
We develop, manufacture and supply our premium products to the world's most important manufacturers in the medical, test & measurement, military and robotics sectors and have been growing very dynamically for 30 years. Proactive acquisition of new customers in south and north ChinaRepresenting our fast growing company at fairs and eventsIndependent recognition of market and customer potentials through own analysis of the customer, market and competition structureBuilding relationships with your existing customer base and maintaining them throughout their life cycleTechnical support for customersUniversity degree in electronic engineering or businessAt least 3-years experience in sales (ideally from the electronics industry) with proven track recordsExcellent communication and presentation skills, high analytical competenceWillingness to travel Build strong, long-lasting customer relationships by partnering with them and understanding their needsFluent in English Working for a German company in an international environmentDistribution of high quality products from the high tech industryHigh level of responsibility and very good personal development opportunitiesRMB 25,000-40,000 /month consisting of a fixed and variable portionYou base in our office in Shenzhen. you will travel frequently to your customers in South and North China.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholdersLead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysisEnsure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activitiesDrive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organizationServe as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related fieldRobust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industryStrong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance managementAdvanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reportingProven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Act as a Senior Finance Business Partner for R&D, Quality/Regulatory, and Medical Affairs, providing financial insights and decision support to senior stakeholders Lead project controlling for R&D projects and clinical studies, including budgeting, forecasting, cost tracking, and performance analysis Ensure transparency of project costs, resource utilization, and key cost drivers to enable effective financial steering of development activities Drive the standardization and continuous improvement of controlling processes, KPIs, and reporting tools across the organization Serve as SAP Key User for CO and PS, supporting project structures, cost allocation logic, and reporting, as well as contributing to SAP ECC6 and S/4HANA implementation and optimization initiatives Degree in Business Administration, Finance, Controlling, or a related field Robust experience in controlling, preferably within the Life Sciences, MedTech, or Pharmaceutical industry Strong background in project controlling for R&D projects or clinical studies, including business case evaluation and financial performance management Advanced SAP expertise, particularly in SAP CO and PS, with experience using SAP BW / Analysis for Office and advanced Excel reporting Proven business partnering and stakeholder management skills, with the ability to challenge senior leaders in a constructive manner; fluent English and solid German skills required Challenging and varied tasks in a promising and innovative industry Flat hierarchies Individual development opportunities Ihr Kontakt Referenznummer 865253/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
DAIICHI SANKYO DEUTSCHLAND GmbH sucht in eine/n (Senior) Medical Information Officer Specialty/Informationsbeauftragter (m/w/d) (ID-Nummer: 13689145)
Unterstützung des Sales/ Außendienstes und der Key Account Management Funktionen, den Bereich Medical und die Marketing Bereichin Bezug auf zugewiesene Vertragsarten, verantwortlich für Vertragserstellung, Vertragsabschluss und Vertragsverlängerung auf der Grundlage genehmigter Vorlagen oder eines Vertragserstellungstools (Engage, KIM)Verwaltung der Buchhaltung für die gesamte vertragsbezogene Korrespondenz und DokumentationEnge Abstimmung mit dem HCP Engagement Expert Team sowie der Finance- Funktionen (P2P) und ProjektverantwortlichenAktive Schulung und Sensibilisierung des Business und der Stakeholder zu Prozessen, Systemen und VertragserstellungProzessierung eingehender HCP-Rechnungen für den internen Workflow inklusive Abstimmung mit der Buchhaltung und Business sowie HCPErstellung und Bearbeitung von Gutschriften innerhalb Engage Ansprechpartner für Kunden und Interessengruppen für alle zugewiesenen VertragsartenPrüfung und Abschluss von Veranstaltungen innerhalb Engage Abgeschlossene kaufmännische, pflegerische, pharmazeutische oder juristische Berufsausbildung oder vergleichbare QualifikationErfahrung und Kenntnisse in Vertragsverhandlungen und im deutschen Compliance- und RechtsumfeldDeutsche Sprachkenntnisse der EU- Klassifizierung C2 und sehr gute Englischkenntnisse (ausländische contract parties) in Wort und SchriftSelbständige, dynamische, strukturierte und engagierte ArbeitsweiseAusgeprägte Kommunikations-, Team- und SozialkompetenzErfahrung in der Buchhaltung, RechnungsbearbeitungSicherer Umgang mit Kommunikationsplattformen wie MS TeamsGute Softwarekenntnisse in der Vertragsmodellierung wie SAP, SRM und Share Point Internationales Unternehmen Ihr Kontakt Ansprechpartner Dennis Karl Referenznummer 865922/1 Kontakt aufnehmen E-Mail: dennis.karl@hays.de Anstellungsart Anstellung bei der Hays Professional Solutions GmbH
Tasks Assisting with surgical procedures, including instrument preparation and intraoperative support Confident handling of medical and technical equipment Patient related administration and accurate documentation Preparation and post-processing of materials and instruments for surgical procedures Supporting the positioning of patients Profile Completed education as a Surgery Technology Assistant (OTA) obtained abroad Recognition notice (Anerkennungsbescheid) issued by the Bavarian State Office for Nursing (Bayerisches Landesamt für Pflege) German language skills at a minimum level of B2, with a willingness to continuously improve your language proficiency Motivation and enthusiasm to work as part of our team and provide support to our patients Friendliness, a strong sense of responsibility, and professionalism Good interpersonal skills in dealing with patients High willingness to learn Motivation and discipline to complete your recognition process in a timely manner Our Offer Support from the Office for International Professionals, assisting you with organizational and administrative matters, as well as preparing for the knowledge examination (Kenntnisprüfung) Accompanied German language course offered during the recognition process Practical trainers specifically assigned to staff undergoing the recognition procedure, ensuring structured onboarding and knowledge development to prepare you for your professional responsibilities Additional qualified and personalized training by your team of experienced colleagues Long-term career perspective at Augsburg’s largest employer, including a permanent employment contract upon recognition Remuneration according to the collective agreement for public service (TV-L), including bonuses for work on Sundays, public holidays, and night shifts Company pension scheme and annual special payment 30 vacation days per year, plus up to 6 additional days for shift work Regulated working hours (38.5 hours/week) with working time account and collectively agreed salary increases Contact Frau Ulrike Kurz, Center Manager, 0821/400-168713 Herr Alexander Wagner, Nursing Educator - Recognition of OTA, 0821/400-168665 Frau Marina Klisanin, Head of Field Office - International Qualified Employees (IFAP), 0821/400-3401 Application Deadline Please upload your documents and submit your application.
Das Unternehmen bietet Raum für Menschen, die Verantwortung übernehmen möchten und Freude daran haben, an anspruchsvollen, zukunftsorientierten Technologien mitzuwirken Weiterentwicklung eines schlanken, risikobasierten Qualitätsmanagementsystems (ISO 13485, AI Act) Sicherstellung regulatorischer Anforderungen für aktive Medizinprodukte, sterile Produkte sowie Software as a Medical Device (SaMD) Vorbereitung, Koordination und Begleitung internationaler Zulassungs- und Registrierungsprozesse (EU/MDR, USA/FDA) inkl.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.