At Oxford Instruments Plasma Technology, we provide tools for the engineering of micro- and nano-structures, with customers using our process solutions to research and produce materials and semiconductors vital for everything from medical devices and diagnostics to electric cars and quantum computers. Benefits: In addition to a competitive starting salary, Oxford Instruments also offers structured career development opportunities, a good work-life balance, private healthcare, a share incentive plan, 25 days of annual leave, half-days on Fridays, a defined contribution Group Personal Pension Plan, and a flexible benefits package that you can tailor to your own requirements.
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.
Prüfung von Sponsoring-Anfragen auf FSA-Konformität, Transparenzvorgaben und interne Standards Herstellung vollständiger Dokumentation gemäß Lilly-Prozessen Abgleich der Anfragen mit strategischen Prioritäten der Brands Budgetmonitoring sowie Erstellung monatlicher Reports für Business, Finance und Compliance. Enge Abstimmung mit Brand Teams, Medical, Legal und Compliance Ansprechpartner für interne Stakeholder und externe Dienstleister (inkl. Vertragsrückfragen) Unterstützung bei System- und Prozessverbesserungen Mitarbeit bei der Weiterentwicklung digitaler Tools, Templates und Dashboards Abgeschlossene kaufmännische Ausbildung oder vergleichbarer Abschluss Berufserfahrung in der Pharmaindustrie oder einem anderen regulierten Umfeld Sehr gute Deutsch- und Englischkenntnisse Hohe Genauigkeit, Verlässlichkeit und Organisationsfähigkeit Sicherer Umgang mit Office-Tools (v.a.
Balda Medical GmbH sucht in Bad Oeynhausen eine/n Quality Compliance Specialist (m/w/d) (ID-Nummer: 12744233)
Prüfung von Sponsoring-Anfragen auf FSA-Konformität, Transparenzvorgaben und interne Standards Herstellung vollständiger Dokumentation gemäß Lilly-ProzessenAbgleich der Anfragen mit strategischen Prioritäten der BrandsBudgetmonitoring sowie Erstellung monatlicher Reports für Business, Finance und Compliance.Enge Abstimmung mit Brand Teams, Medical, Legal und ComplianceAnsprechpartner für interne Stakeholder und externe Dienstleister (inkl. Vertragsrückfragen)Unterstützung bei System- und ProzessverbesserungenMitarbeit bei der Weiterentwicklung digitaler Tools, Templates und Dashboards Abgeschlossene kaufmännische Ausbildung oder vergleichbarer AbschlussBerufserfahrung in der Pharmaindustrie oder einem anderen regulierten UmfeldSehr gute Deutsch- und EnglischkenntnisseHohe Genauigkeit, Verlässlichkeit und OrganisationsfähigkeitSicherer Umgang mit Office-Tools (v.a.
Allianz Private Krankenversicherungs-AG sucht in eine/n Medical Risk Analyst (m/w/d) (ID-Nummer: 13753373)
International assignments; Exclusive employee benefits/discounts; Further training and education; Medical, Dental and Vision coverage; Multiple career opportunities; Talent development; Team Events; Trust-based working time; 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.
About us Your Contribution Lead, coach, and motivate employees within respective area of responsibility, while providing direction to achieve department goals and objectivesAssist in developing department budget and investment plan(s) according to strategic goalsCultivate employee talent through training and coaching measures, while also conducting employee performance reviewsSupport the development and updating of Quality Assurance programs, policies, processes, procedures and controlsReview, analyze and report on quality discrepancies related to SCHOTT products, while developing disposition and corrective actions for product discrepanciesManage the review of batch records and avoid impacting shipment datesManage Department Training Coordinator activities and projectsManage document control activities to include, releasing, archiving, tracking and reporting of the document review process for controlled documentsLead and support the implementation of Systems and Compliance Improvements including site compliance, along with data integrity requirementsMeasure and analyze Quality System trendsOversee the internal audit function to ensure ongoing compliance to the Quality Management System (QMS)Maintain the Archive Room and document retention requirementsWrite and revise Standard Operating Procedures (SOPs) and provide training, as requiredManage the CAPA and Change-Control process to include, issuing, reviewing and approving stepsSupport all customer or registrar quality related audits and/or evaluationsUtilize quality tools, including Compliant-PRO, etc., for information, tracking and reporting purposes, as required by the Pharm Business UnitManage assigned CAPA(s) by performing root cause investigations, while defining resolution actions; implement preventive and corrective actions in a timely manner as a result of customer complaints or customer audit findingsHelp promote and implement safety/EHS directives and maintain a clean and safe workspaceAssure compliance with ISO certifications and cGMP, along with adherence to Company policies and procedures and Code of Conduct/safety guidelines Your Profile Bachelor’s Degree in Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language 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 Chemistry, Biology, Engineering or science related field, requiredMinimum three years of experience in Quality leadership roleSolid knowledge of ISO 9001, 14001, 15378, along with cGMP and ISOExposure to the glass forming industry and/or pharmaceutical industry, preferredThorough MS Office applications, SAP and electronic QMS systemsMulti-tasking abilitiesDecision makingDetail oriented approachForward/creative thinkingService orientedEffective communication skillsAbility to read, write and speak English language
This includes the ability to work unsupervised, under pressure and meet deadlines • Creative with strong commitment to quality and excellence, and a continuous improvement mindset • Communication and time-management skills • Strong analytical skills and efficient problem solving • You are educated on master degree level in IT Security, Computer Science or equivalent, fluent in English WHAT IS THE PLUS POINT (S): • Certifications such as SEC545 (SANS), CCSP(ISC2), CISSP, CCSK(CSA), Microsoft Certified Azure Security or similar • DevSecOps experience related to application deployments on multi cloud • Strong experience on cloud platforms such as Google, Amazon and Azure WHAT YOU WILL GET FROM US: • Great team of IT professionals with global working exposure • On-going professional and technical training and certifications • Global internal job opportunities available within DPDHL • A multicultural environment • Meal Card and Flexible Benefits – customized according to individual needs • Choose any day for your vacation from earned public holiday (Saturday and ad hoc) • Smart casual dress code • Company Outpatient Medical • Home office possibilities Sounds good? Start your application now! Location: GER / PRG
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.
Key Responsibilities Overall management and coordination of site operations in the Automotive environment in accordance with defined processes, standards, and management instructionsDisciplinary and functional leadership, development, and motivation of site employeesPlanning and control of personnel deployment, capacity management, and vacation schedulesEnsuring compliance with Automotive-specific quality, occupational health, safety, and environmental requirementsOrganization and documentation of safety briefings, instructions, risk assessments, and emergency measuresResponsibility for workplace organization, tools, equipment, and operational resourcesCoordination of operational planning, order execution, reporting, and documentationReview and approval of operational reports, time confirmations, and performance dataActive implementation and monitoring of Continuous Improvement (KVP) initiativesOrganization of first aid readiness and required occupational medical examinationsActive communication and enforcement of safety and health protection measuresMaintenance and development of customer relationships at the assigned operational sitesConfident use of SAP for operational processesBusiness development in the surrounding area.
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.
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.
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.
For our esteemed client in the pharmaceutical industry, we are looking for a Supplier Quality Engineer Packaging (m/f/d) based in Bad Homburg. Become part of a globally leading company in medical devices and pharmaceuticals and take responsibility for qualifying packaging suppliers and driving the global harmonization of packaging standards.
YOUR TASKS You consistently enforce HSE and safety requirements on site and intervene immediately in case of deviations You provide technical coordination and supervision of external contractors during mechanical installation activities You ensure quality, quantity, and compliance of installation work and initiate corrective actions when requirements are not met You ensure timely completion of work as the basis for proper commissioning of the wind turbine systems You review turbine-related reports and documentation for completeness, accuracy, and up-to-date status You actively participate in project and site meetings and contribute your expertise as a Mechanical Supervisor You identify missing or defective components and promptly report requirements to the site management YOUR PROFILE Completed technical vocational training, for example as a mechatronics technician or industrial mechanic, or an equivalent qualification gained through long-term experience in the wind energy sector Willingness to undertake multi‑week assignments on construction sites as well as regular Saturday work High willingness to travel mainly within Germany, with occasional assignments in Austria and the Netherlands Medical fitness for working at heights as well as confined working space and good physical condition for work on wind turbines Confident PC user skills, especially in MS Office Good command of English, both written and spoken, for collaboration in international teams High resilience, structured problem-solving skills, and clear, transparent communication Valid driving license class B We provide the opportunity for further qualification as an industrial electrician.
YOUR TASKS You consistently enforce HSE and safety requirements on site and intervene immediately in case of deviations You provide technical coordination and supervision of external contractors during mechanical installation activities You ensure quality, quantity, and compliance of installation work and initiate corrective actions when requirements are not met You ensure timely completion of work as the basis for proper commissioning of the wind turbine systems You review turbine-related reports and documentation for completeness, accuracy, and up-to-date status You actively participate in project and site meetings and contribute your expertise as a Mechanical Supervisor You identify missing or defective components and promptly report requirements to the site management YOUR PROFILE Completed technical vocational training, for example as a mechatronics technician or industrial mechanic, or an equivalent qualification gained through long-term experience in the wind energy sector Willingness to undertake multi‑week assignments on construction sites as well as regular Saturday work High willingness to travel mainly within Germany, with occasional assignments in Austria and the Netherlands Medical fitness for working at heights as well as confined working space and good physical condition for work on wind turbines Confident PC user skills, especially in MS Office Good command of English, both written and spoken, for collaboration in international teams High resilience, structured problem-solving skills, and clear, transparent communication Valid driving license class B We provide the opportunity for further qualification as an industrial electrician.
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.
We know: motivated and committed employees are the precondition for the success of our company. Medical, Dental and Vision coverage; Free Parking; Holistic corporate health management; Multiple career opportunities; Social Insurance System; Talent development; Team Events 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 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.
Löwenstein Medical SE & Co. KG sucht in eine/n Manager internationale Messeorganisation (m/w/d) (ID-Nummer: 13753318)
Löwenstein Medical SE & Co. KG sucht in eine/n Data Engineer / Microsoft Fabric Engineer (m/w/d) (ID-Nummer: 13752950)
Mitwirkung bei verschiedenen Projekte der Bereiche Qualitätssicherung und GMP direkt bei unseren Kunden vor Ort mit Unterstützung namhafte Hersteller im GMP-regulierten Umfeld (Pharma, Biotechnologie, Life Sciences, Medical Devices, Chemie) bei der Erfüllung ihrer Qualitätsansprüche und Entwicklung neuer Lösungsansätze Qualifizierung von Anlagen und Validierung von Prozesse nach den neuesten Methoden und messtechnischen Standards als Projektkoordinator:in oder -leiter:in auch Verantwortung Projekten Durchführung des Hygienemonitoring im Rahmen des Hygienemanagements Sie sind Betreuer:in und Berater:in für die vielfältigen Fragestellungen in der Qualitätssicherung und GMP-Compliance Ihr Profil: abgeschlossenes Ingenieurstudium (Master, Bachelor, Promotion) der Fachrichtungen Chemie, Pharmatechnik, Biotechnologie, Verfahrenstechnik oder einer vergleichbaren naturwissenschaftlichen Fachrichtung sowie Erfahrung mit dem Schwerpunkt von Prozessvalidierungen im Bereich Medizinprodukte, biologische Produkte oder Pharmazeutika Reisebereitschaft (40 %), sehr gute Deutsch- und Englischkenntnisse Sicherer Umgang mit den gängigen SAP und MS Office-Programmen als ein:e Macher:in oder ein:e ‚Anpacker:in‘ und haben Sie ein freundliches und Service orientiertes Auftreten hohes Maß an Selbstständigkeit, Engagement und Teamspirit sowie Bereitschaft Verantwortung zu übernehmen Freude Haben wir Ihr Interesse geweckt?
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
Ursapharm Arzneimittel GmbH sucht in Saarbrücken eine/n Referent (m/w/d) Medical Information (ID-Nummer: 13464987)
Nippon Gases Deutschland Holding GmbH sucht in eine/n Gebietsverkaufsleiter*in Medical Südwest (ID-Nummer: 13723955)
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 Dokumentation Enge Abstimmung mit dem HCP Engagement Expert Team sowie der Finance- Funktionen (P2P) und Projektverantwortlichen Aktive Schulung und Sensibilisierung des Business und der Stakeholder zu Prozessen, Systemen und Vertragserstellung Prozessierung eingehender HCP-Rechnungen für den internen Workflow inklusive Abstimmung mit der Buchhaltung und Business sowie HCP Erstellung und Bearbeitung von Gutschriften innerhalb Engage Ansprechpartner für Kunden und Interessengruppen für alle zugewiesenen Vertragsarten Prüfung und Abschluss von Veranstaltungen innerhalb Engage Abgeschlossene kaufmännische, pflegerische, pharmazeutische oder juristische Berufsausbildung oder vergleichbare Qualifikation Erfahrung und Kenntnisse in Vertragsverhandlungen und im deutschen Compliance- und Rechtsumfeld Deutsche Sprachkenntnisse der EU- Klassifizierung C2 und sehr gute Englischkenntnisse (ausländische contract parties) in Wort und Schrift Selbständige, dynamische, strukturierte und engagierte Arbeitsweise Ausgeprägte Kommunikations-, Team- und Sozialkompetenz Erfahrung in der Buchhaltung, Rechnungsbearbeitung Sicherer Umgang mit Kommunikationsplattformen wie MS Teams Gute 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
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.
Working knowledge of a broad range of packaging materials, packaging equipment and packaging lines commonly found within the Food, Beverage or consumer industries Experience with development of large packaging project proposals Equivalent combination of education and experience will be considered Benefits Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
Working knowledge of a broad range of packaging materials, packaging equipment and packaging lines commonly found within the Food, Beverage or consumer industries Experience with development of large packaging project proposals Equivalent combination of education and experience will be considered Benefits Medical, Dental, Vision insurance offered at 30 days of employment Generous Educational Reimbursement program Company sponsored Life and Disability Insurance Paid Time Off Ten (10) Paid Holidays per year 401K with Company Match Location: Waukesha ǀ Wisconsin ǀ USA
We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma.
TUTOGEN Medical GmbH sucht in eine/n Leitung Qualitätsmanagement international / Sachkundige Person nach § 14 AMG (m/w/d) (ID-Nummer: 13674376)
April einen Evaluation Engineer (m/w/d) Design Verification & Medical Devices in Vollzeit. Ein flexibles Arbeitsmodell mit der Möglichkeit zum mobilen Arbeiten ist gegeben, jedoch sind regelmäßige Präsenztage vor Ort in Ingelheim erforderlich.
Wir entwickeln, fertigen und liefern unsere Premiumprodukte an die wichtigsten Hersteller in aller Welt in den Branchen Medical, Test&Measurement, Military, Robotics und wachsen seit über 30 Jahren sehr dynamisch. Als Legal Counsel / Syndikusanwalt (m/w/d) sind Sie zentraler rechtlicher Sparringpartner in einem international aufgestellten Unternehmensumfeld mit Standorten in Deutschland, USA, Vietnam, China und Hong Kong.
Fonterra is a co-operative owned by around 9,000 New Zealand dairy farmers. Fonterra’s focus is on Active Living, Medical Nutrition and Infant Dairy and with this variety of products Fonterra reaches markets in China, Japan, Indonesia, America, Europe and more.
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.
About Convatec Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care.
Löwenstein Medical Technology GmbH + Co. KG sucht in eine/n Innovationsmanager AI / KI-Enablement Specialist (m/w/d) (ID-Nummer: 13764241)
Heraeus Medical GmbH sucht in eine/n MES & SAP Key User (m/w/d) (ID-Nummer: 13677556)
Fresenius Medical Care Deutschland GmbH sucht in eine/n (Senior) Data Privacy Engineer (m/f/d) / (Senior) Expert (m/f/d) – Technical Privacy (ID-Nummer: 13676634)
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.
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.
Provide strategic and therapeutic area guidance for clinical development plans in compliance with applicable regulatory, medical, and ethics guidelines. Ensure high-quality, data-driven deliverables that meet the highest standards of medical, ethical, and scientific integrity and conduct.
Study Physician services Medical Content Oversight: Responsible for medical content in Clinical Trial Protocols (CTPs).Collaborates with Project Management, Patient Safety, Medical Writers, and trial/evidence teams.Provides medical input for CTP updates.
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.
Develop and maintain software solutions by applying in-depth technical knowledge and problem-solving skills, while ensuring compliance with regulatory standards for medical softwareEnsure the timely delivery of high-quality software for medical devices that meets both the company's standards and customer needs, influencing the success of the team and broader project outcomesCommunicate complex technical concepts effectively, fostering an environment of collaboration and continuous learning within and across diverse and intercultural teamsEmpower your team members to take ownership of their work and leading by example to foster teamwork and mentorship Degree or equivalent practical experience in a specialized field related to software development or engineeringProven experience in software development, with a demonstrated passion and hands-on professional experience working with Rust incl. a solid understanding of Rust's core concepts (ownership, borrowing, and lifetimes), experience with asynchronous programming in Rust (e.g., using async/await) and familiarity with common Rust libraries and frameworks (e.g., tokio, actix-web, rocket, serde, sqlx).Capable of solving complex issues creatively and effectively, using a multi-faceted approach based on thorough analysis to resolve complex technical challengesExcellent communication skills with the ability to foster an inclusive and diverse environment as well as collaborate effectively within and across teamsEnglish fluency is a prerequisite, German is advantageous Internal career opportunitiesWorld-renowned medical devices company Ihr Kontakt Referenznummer 858105/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt