Sie sind hier: Home > Regional > !#platzhalterstadtname!# >

!#platzhalterdienstname!#

Anzeige
Filter

Pharmazie: 23 Jobs in München

Berufsfeld
  • Pharmazie
Branche
  • Pharmaindustrie 16
  • Gesundheit & Soziale Dienste 3
  • Medizintechnik 2
  • Sonstige Branchen 1
  • Wissenschaft & Forschung 1
  • Öffentlicher Dienst & Verbände 1
Berufserfahrung
  • Mit Berufserfahrung 22
  • Ohne Berufserfahrung 8
  • Mit Personalverantwortung 4
Arbeitszeit
  • Vollzeit 21
  • Home Office 3
  • Teilzeit 3
Anstellungsart
  • Feste Anstellung 19
  • Befristeter Vertrag 3
  • Studentenjobs, Werkstudent 1
Pharmazie

Senior Manager Clinical Safety Scientist (m/f/x)

Sa. 19.06.2021
München
Daiichi Sankyo is dedicated to creating new modalities and innovative medicines by leveraging our world-class science and technology for our purpose “to contribute to the enrichment of quality of life around the world”. In addition to our current portfolio of medicines for cancer and cardiovascular disease, Daiichi Sankyo is primarily focused on developing novel therapies for people with cancer as well as other diseases with high unmet medical needs. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation to realize our 2030 Vision to become an “Innovative Global Healthcare Company Contributing to the Sustainable Development of Society”. For our headquarter in Munich we are seeking highly qualified candidates to fill the position: Senior Manager Clinical Safety Scientist (m/f/x) The Senior Manager, Clinical Safety Scientist, will handle aspects of signal identification, evaluation, and risk mitigation across therapeutic areas, in collaboration with product safety leads. This position proactively creates communication plans for important safety topics and identified risks. This position may serve as primary author for certain safety documents and regulatory submissions (NDA/BLA in US and MAA in EU). Additionally, this position project manages larger Phase 3 Studies, Safety Management Team (SMT) meetings and supervises junior scientist to work together as a team. This position works closely with CSPV staff, SMT members and other functions. Roles and responsibilities: Oncology Product Risk Management support for pivotal clinical studies and BLA/MAA activities A key participant in developing and implementing the risk management strategy for assigned oncology products Works with Product Safety Physician for pivotal clinical study maintenance Works with Product Safety Physician to support regulatory submissions (NDA/BLA in US and MAA in EU) and develops the strategy for risk minimization activities for post- marketing Risk Management (Signal identification, evaluation, mitigation) and Safety Communication Support Product Safety Physician for signal discussion at Safety Management Team (SMT) Independently integrates and analyses safety data from multiple sources to deliver comprehensive conclusions Independently identifies gaps in safety surveillance plans/RMPs and escalates appropriately Develops strategy for communicating safety information internally and externally in collaboration with product safety lead Leads the development of safety communication documents and aggregate safety reports Project Management Serves as Project Management for Signal Management and Safety Management Team devoted to larger Phase 3 products and ensures adherence to project timeline Responsible for Signal Tracking and Deviation Management with safety related activities (e.g. RMP) Bachelor’s degree at minimum required; PharmD or PhD preferred 5 years of experience with an advanced degree; 7 years of experience with a bachelor’s degree Possesses strong medical and drug development knowledge Experience in summarizing and presenting safety data Experience in NDA/BLA and/or MAA submission activity Strong communication skills Experience in project management and working in a matrix environment International, European and PV laws Fluent business English (oral and written) We offer an interesting, diversified and challenging position, good contractual conditions, flexible working models, all the social benefits of a modern company and a professional environment where you will have the opportunity for personal growth.
Zum Stellenangebot

Scientist (w/m/d) Drug Product Development for Biopharmaceuticals

Fr. 18.06.2021
Planegg
Coriolis Pharma, is a globally operating independent service provider for formulation research and development of (bio)pharmaceutical drugs (proteins, peptides, monoclonal antibodies, RNA/DNA etc.) and vaccines. An interdisciplinary team of highly qualified scientists with many years of experience in the development of (bio)pharmaceuticals supported by an expert scientific advisory board provides cutting-edge service and know-how related to the formulation development of biopharmaceuticals. Scientist (w/m/d) Drug Product Development for Biopharmaceuticals Support/lead project teams for the pharmaceutical drug product development of biopharmaceuticals Plan and execute CMC activities of biopharmaceuticals, including formulation preparation and development, forced degradation study, stability and comparability testing, primary packaging selection, optimization of lyophilization processes, robustness investigations, scale-up and transfer, etc. Perform analytical method development, characterization and evaluation of biopharmaceuticals Data analysis of analytical results,  support of reporting activities Communication and reporting with our customers System ownership of analytical equipment (e.g. maintenance activities) University degree in pharmacy, pharmaceutical sciences, (bio)chemistry, chemical engineering, or related field A minimum of 3 years relevant experience Strong scientific background and experience in the field of biopharmaceutical characterization and analysis Experience in the field of protein/oligonucleotide liquid and/or lyophilization formulation development and formulation preparation technology is advantagous Open for new ideas and tasks, high willingness to learn - hands on mentality Team player with strong motivation, inter-personal skills and excellent communication abilities As Scientist, you will join a highly motivated, interdisciplinary team performing contract research and development for customers from the (bio)pharmaceutical industry worldwide. We offer you diversified and challenging areas of responsibilities in our innovative company. We actively support your personal development (technical, scientific and personal skills) especially by training on relevant techniques for characterization of (bio)pharmaceuticals. Beyond that Coriolis offers a variety of benefits and team activities to its employees.
Zum Stellenangebot

Junior Scientist (m/w/d) Protein Liquid Formulation / Lyophilization Development

Fr. 18.06.2021
Planegg
Coriolis Pharma, is a globally operating independent service provider for formulation research and development of (bio)pharmaceutical drugs (proteins, peptides, monoclonal antibodies, RNA/DNA etc.) and vaccines. An interdisciplinary team of highly qualified scientists with many years of experience in the development of (bio)pharmaceuticals supported by an expert scientific advisory board provides cutting-edge service and know-how related to the formulation development of biopharmaceuticals. Junior Scientist (m/w/d) Protein Liquid Formulation / Lyophilization DevelopmentAs a Junior Scientist, you will join a highly motivated, interdisciplinary team performing contract research and development for customers from the (bio) pharmaceutical industry worldwide. Support project teams for the pharmaceutical drug product development of biopharmaceuticals Formulation development activities (e.g., preparation of liquid and/or freeze-dried samples for (pre)formulation study) Analytical characterization of liquid and/or freeze-dried samples with respect to quality attributes Perform data analysis, support of reporting activities Internal discussion of data within the project team Participation in meetings, also with our international customers System ownership of analytical equipment (e.g. maintenance activities) University degree in a related field (biotechnology, pharmacy, (bio)chemistry, chemical engineering, biology etc.) Preferably experience in the field of protein formulation (liquid or lyophilization products) and protein analytics Team player with strong motivation, inter-personal skills and excellent communication abilities Open for new ideas and tasks, high willingness to learn We offer you diversified and challenging areas of responsibilities in our innovative company. As a Junior Scientist you’ll become part of a highly motivated, interdisciplinary team to work and share ideas with. We actively support your personal development (technical, scientific and personal skills) especially by training on relevant techniques for characterization of biopharmaceuticals. Beyond that Coriolis offers a variety of benefits and team activities to its employees.
Zum Stellenangebot

Regulatory Affairs Manager (m/w/d)   

Do. 17.06.2021
Gröbenzell
Die Glenmark Arzneimittel GmbH mit Sitz in Gröbenzell bei München (Tochtergesellschaft der Glenmark Pharmaceuticals Ltd., Mumbai) konnte sich seit ihrer Gründung im Jahr 2010 mit qualitativ hochwertigen Arzneimitteln im deutschen Generikasegment unter den Top 20 Pharmaunternehmen etablieren.1 Das Portfolio von Glenmark umfasst viele Indikationsgruppen, wobei der Schwerpunkt auf den Therapiebereichen Zentrales Nervensystem (ZNS), Herz-Kreislauf-System (HKS) und Respirationssystem liegt. Glenmark ist mit vielen Produkten Vertragspartner von großen Krankenkassen und leistet somit einen Beitrag für eine breite und bezahlbare Arzneimittelversorgung. Glenmark Pharmaceuticals Ltd. ist ein internationales forschendes Pharmaunternehmen mit Sitz in Mumbai, Indien. Der Fokus des Unternehmens liegt auf der Erforschung innovativer chemischer und biologischer Wirkstoffe. Darüber hinaus bietet Glenmark ein breites Portfolio von patentfreien Arzneimitteln. Glenmark beschäftigt rund 13.500 Mitarbeiter in über 80 Ländern und betreibt neben 17 Produktionsstätten auch fünf hochmoderne Forschungszentren, eines davon in Neuchâtel in der Schweiz. Glenmark Pharmaceuticals Ltd. zählt zu den 80 umsatzstärksten Pharma- und Biotechnologieunternehmen weltweit.2 Zur Unterstützung unseres Teams suchen wir zum nächstmöglichen Zeitpunkt einen Regulatory Affairs Manager (m/w/d)    befristet auf 2 Jahre  In dieser Position sind Sie verantwortlich für die Koordination und Durchführung von zulassungsrelevanten Aufgaben für die Ihnen zugeordneten Produkte für den deutschen Markt. Sie pflegen Kontakte zu deutschen Behörden und leiten ein Team von 2 Mitarbeitern. Zu Ihren Hauptaufgaben zählen: Hauptverantwortlicher interner und externer Ansprechpartner für regulatorische Fragestellungen für Deutschland Leitung des deutschen Regulatory Affairs Teams und Koordination und Verteilung der Projekte und Aufgaben Überwachung von Deadlines für regulatorische Projekte Erstellung der deutschen Produktinformationstexte gemäß dem jeweiligen Referenzprodukt und deren Überarbeitung nach beispielsweise PSUSA-Verfahren/PRAC-Empfehlungen oder sonstige Änderungen Betreuung der deutschen nationalen Phase für Neuzulassungen nach DCP/MRP-Verfahren Fristgerechte Erstellung, Prüfung und Freigabe von Druckvorlagen für Packungsmaterialien und Gebrauchs- und Fachinformation sowie Koordination und Absprache mit internen und externen Stakeholdern für deren fristgerechte Implementierung Erstellung und elektronische Einreichung von Variations / nationalen Änderungsanzeigen und Renewals über CESP-Portal bzw. PharmNet.Bund Einreichung generischer Zulassungsanträge (DCP/MRP und rein nationale Verfahren) und deren Betreuung während des Verfahrens Mitarbeit in internationalen Projektteams Dokumentation gemäß interner Richtlinien (SOP Compliance) Pflege der regulatorischen Datenbanken intern sowie extern (beispielsweise BfArM PIT-Portal und Sunset-Clause-Datenbank) Abgeschlossenes Studium der Pharmazie, Medizin, Naturwissenschaft oder vergleichbare Qualifikation Mind. 3 Jahre einschlägige Berufserfahrung im Bereich Arzneimittelzulassung Erste Erfahrung im Führen von Mitarbeitern vorteilhaft Aktuelles Fachwissen zu arzneimittelrelevanten Gesetzen und Richtlinien Gute Kenntnisse im MS-Office Paket Deutschkenntnisse auf Muttersprache-Niveau zwingend erforderlich Sehr gute Englischkenntnisse Selbstständige und sehr genaue Arbeitsweise Sie übernehmen gerne Verantwortung und bringen eine Hands-on-Mentalität, Zuverlässigkeit und Engagement mit Sicheres, kommunikationsstarkes Auftreten Flexibilität und Belastbarkeit sowie engagierte Persönlichkeit
Zum Stellenangebot

Head of Regional Access Management SBD (m/w/d)

Do. 17.06.2021
München
Daiichi Sankyo entwickelt neue Modalitäten und innovative Medikamente. Wir nutzen unsere erstklassige Forschung und Technologie, um weltweit unseren Beitrag zu einer verbesserten Lebensqualität zu leisten. Zusätzlich zu unserem derzeitigen Portfolio von Medikamenten gegen Krebs sowie kardiovaskuläre Erkrankungen konzentriert sich Daiichi Sankyo insbesondere auf die Entwicklung neuer Therapien für Menschen mit Krebs und anderen Krankheiten mit hohem ungedecktem medizinischem Bedarf. Unsere starke Entwicklungspipeline baut auf einer über einhundertjährigen Forschungsgeschichte auf. 16.000 Mitarbeiter in über 20 Ländern tragen zu unserer Vision bei, bis 2030 ein innovatives globales Unternehmen im Gesundheitswesen zu werden, das zu einer nachhaltigen Entwicklung der Gesellschaft beiträgt. Ab sofort suchen wir bei der Daiichi Sankyo Deutschland GmbH eine/n engagierte/n Head of Regional Access Management SBD (m/w/d) In Ihrer Funktion sind Sie in das Specialty Business Division Market Access Team als Führungsfunktion eingebunden und übernehmen folgende Aufgaben: Fachliche und disziplinarische Führung eines Regional Market Access Manager SBD-Teams Unterstützung in der strategischen Entwicklung cross-funktionaler Account Pläne in enger Abstimmung mit den Vertriebsregionen Erarbeitung und Umsetzung der regionalen Market Access Strategie unter Berücksichtigung der Brandpläne sowie der Produkt-Positionierung mit dem Regional Access Team Definition von KPIs für das Regional Market Access Team sowie strategische Ausrichtung und Ressourcenverteilung des Teams mit Blick auf das Produktportfolio Analyse, Bewertung und Entwicklung von strategischen Handlungsoptionen für das Product Leadership Team für regionale Market Access Themen mit dem Fokus auf kardiovaskuläre Indikationsgebiete (Wirtschaftlichkeit, Erstattung, Preisgestaltung, Kooperationen mit Stakeholdern wie Krankenkassen & Kassenärztliche Vereinigungen, Klinikapotheken und regionalen Verbänden) mit Relevanz für den Erfolg von Daiichi-Sankyo Generierung von Insights mit dem Regional Market Access Team im Zusammenhang mit der Erarbeitung von Access Launch Strategien Umsetzung regionaler Launch Access Strategien mit fortlaufendem Monitoring & Reporting Monitoring der regionalen Market Access Landschaft mit Blick auf Opportunitäten für die cross-funktionale Marktbearbeitung Coaching und Mitarbeiterentwicklung Erfolgreich abgeschlossenes Studium der Gesundheitsökonomie/ Wirtschaftswissenschaft, Medizin, Pharmazie oder Naturwissenschaft Langjährige Erfahrung in der Führung von regionalen Teams vorzugsweise mit Coaching Kenntnissen Erfahrung im Key Account Management (Krankenhäuser, Krankenhausapotheken) Mindestens sechs Jahre Berufserfahrung im Market Access Bereich (Pharmazeutische Industrie, Krankenkasse, Gesundheitsdienstleistung) Kenntnisse im Herz-Kreislaufbereich Englisch- und gute MS-Office-Kenntnisse Persönliche Anforderungen: Für diese Aufgabe suchen wir eine flexible und kommunikationsstarke Persönlichkeit, die es versteht, in cross-funktionalen Teams zu arbeiten und das Team zu motivieren sowie zu positionieren. Sie verfügen über sehr gute analytische Fähigkeiten, können komplizierte Zusammenhänge zielgruppengerecht darstellen und bringen eine hohe Problemlösungskompetenz mit. Ein eigenmotivierter und zielorientierter Arbeitsstil sind dabei ebenso unerlässlich wie gute Organisations- Dokumentations- und Präsentationsfähigkeiten. Idealerweise wohnen Sie in München oder im Süden Deutschlands. Als internationaler Arbeitgeber in einem Zukunftsmarkt sind uns ein attraktives und facettenreiches Angebot an Leistungen über das Gehalt hinaus wichtig. Wir bieten Ihnen neben einem leistungsgerechten Einkommen vielfältige weitere Benefits wie z.B. eine betriebliche Altersvorsorge, flexible Arbeitszeiten, ein zeitgemäßes Mobility Angebot, diverse Sportangebote u.v.m.
Zum Stellenangebot

Scientist Preclinical Development, Safety and Toxicology (F/X/M)

Mi. 16.06.2021
Gräfelfing
Immunic AG is a dynamic biotechnology company located in Gräfelfing (near Munich). We are a specialist in selective oral drugs in immunology and focused on developing novel oral therapies with best-in-class potential for chronic inflammatory and autoimmune diseases. Currently, we have three drug development projects in different clinical stages ofdevelopment, including our most advanced drug that will enter phase 3 clinicaltrials in different medical indications. Immunic is an exciting place for fresh ideas – apply now and become part of our team! We are looking for a Scientist Preclinical Development, Safety and Toxicology (F/X/M) We are looking for a scientist who will help us to drive our preclinical projects. You would be working in a team with experienced scientist and support our Chief Scientific Officer.Act as study monitor and manage multiple IND-enabling preclinical studies (GLP / non-GLP compliant, single and multi-site) performed at external contract research organizations (CROs)Coordinate, plan, and monitor preclinical safety and tolerability studies for all development programsAssist study protocol development, review study results, reports, regulatory files, and any other study-related documentationSupport qualification and selection of preclinical CROs and maintain regular interaction with CROs to ensure quality, proper information flow and contract performanceManage study operations logistics (e.g., compound delivery to sites, multi-site shipment of samples)Be responsible for scientific communications (internally and with CROs)You have a scientific background in toxicology, biology, chemistry, pharmacy, veterinary medicine, or other relevant scientific discipline (at least Master's degree).A minimum of 2 years of experience in the design and execution of preclinical studies in a pharmaceutical industry company or Preclinical Research OrganizationIn-depth understanding of toxicology and working knowledge with animal models is a plus (handling, drug administration, anesthesia, organ harvest, tissue histology and quantitative microscopy, etc.)Sound knowledge of GLP principles and international drug development guidance (EMA, FDA, ICH).Project management experience with focus on early-stage drug developmentExcellent interpersonal skills and ability to work in a team environmentVery good written and oral communication skills in English language (German is a plus)A full-time position (or part time, minimum 30 hours)A fair salary commensurate with your experienceYou can participate in the success of our companyA highly innovative and motivated team where you can rely on your colleaguesCross-functional work experience withing an international team and flat hierarchies
Zum Stellenangebot

Assistenz (w/m/d) im Bereich Arzneimittelzulassung

Mi. 16.06.2021
München
Assistenz (w/m/d) im Bereich Arzneimittelzulassung Die DENK PHARMA GmbH & Co. KG ist als modern geführtes Unternehmen in mehr als 80 Ländern tätig. Unser Ziel ist der Zugang zur Heilung. Deshalb bieten wir unseren Patienten weltweit die gleiche hochwertige Arzneimittelqualität an, wie sie in jeder deutschen Apotheke zu finden ist. Um dies sicherzustellen, werden unsere Produkte in Deutschland zugelassen, hergestellt und auf ihre Qualität kontrolliert. Wachse mit uns – am Hauptsitz in München Bogenhausen! Das Zulassungsteams bei der Neuregistrierung von Arzneimitteln/Nahrungsergänzungsmitteln und der Pflege bestehender Zulassungen in unseren Exportländern zu unterstützen Erstellung und Pflege regulatorischer Dokumente nach Anweisung Organisation von Dokumentenbeglaubigungen Die Pflege von Dokumenten-Management-Systemen und Datenbanken Kopier- und Sortierarbeiten Abteilungsintern organisatorische und administrative Aufgaben durchzuführen  Eine erfolgreich abgeschlossene Berufsausbildung (z.B. PTA/MTA/CTA oder Fremdsprachen-korrespondenz) oder eine vergleichbare Qualifikation Sehr gute Englisch- oder Französischkenntnisse Eine strukturierte, zuverlässige und genaue Arbeitsweise Den Wunsch und die Fähigkeit, Teil eines starken Teams zu sein Gute PC-Kenntnisse, Interesse an elektronischer Bearbeitung und Verwaltung von Dokumenten und Daten Teil eines dynamischen Teams zu werden und aktiv das Unternehmen mit deinen Stärken zu kreieren und mitzugestalten Ein vielfältiges Angebot an Weiterbildungsmöglichkeiten, durch welche du dich persönlich und auch beruflich weiterentwickeln kannst Mitarbeiterbenefits, wie z.B. Fitness Kooperation und vieles mehr Regelmäßige Teamevents und zahlreiche Firmenfeiern 30 Tage Urlaub pro Jahr, extra Urlaubstag bei Unternehmenszielerreichung
Zum Stellenangebot

Medical Director or Medical Monitor (m/f/d) – Flexible Part Time Opportunity –

Mi. 16.06.2021
Gräfelfing
Immunic AG is a dynamic biotechnology company located in Gräfelfing (near Munich). We are a specialist in selective oral drugs in immunology and focused on developing novel oral therapies with best-in-class potential for chronic inflammatory and autoimmune diseases. Currently, we have three drug development projects in different stages of clinical development, including our most advanced drug candidate that will enter phase 3 clinical trials, soon. Immunic is an exciting place for fresh ideas – apply now and become part of our team! We are looking for a Medical Director or Medical Monitor (m/f/d) – Flexible Part Time Opportunity – We are looking for a physician (MD degree) who is interested in supporting us with the execution of clinical trials as a Medical Monitor or Medical Director in a part-time position. We would be open to flexible working hours to combine private responsibilities or other part-time clinical work. Preferably, we are looking for a physician who is based in the Munich area and who can work in Immunic’s office as well as from home. As a Medical Director (Medical Monitor) (m/f/d), you would be working in a team with experienced clinical project managers and support the Chief Medical Officer in keeping track of the medical aspects of Immunic’s clinical trials. The assignment can be discussed based on prior therapeutic experience.Drive the development of the clinical study protocols, revisions, and amendments, when necessaryBe responsible for medical monitoring and ongoing medical data review for clinical trial activities including medical oversight of the protocol exemptions, violations, eligibility issues, concomitant medications, and general medical-related issuesBe responsible for pharmacovigilance for assigned projects as well as overseeing ongoing safety reviews, including adverse events and lab abnormalitiesCoordinate and oversee the medical monitors at the CROsAct as primary contact for CROs regarding medical questionsMD degree and experience in pharmaceutical clinical trials (either on the sponsor or CRO side or as an investigator).Experience in the clinic or with clinical trials, gastroenterology, hepatology, immunology, internal medicine, or emergency medicine would be beneficial.You enjoy working in a dynamic work environment where you can structure your work independently and drive processes.You have a hands-on mentality.You are fluent in English in verbal and written form (conversational skills in German preferred but not required).You don’t have experience in industry yet? We encourage and support our employees to take on responsibilities. At Immunic, you can grow with your experience.A part time position (20 to 30 hours) with flexible arrangements to match your needsA fair salary commensurate with your experienceYou will participate in the success of our companyA highly innovative and motivated team where you can rely on your colleagues
Zum Stellenangebot

Product Support Specialist (f/m/d)

Di. 15.06.2021
Germering, Oberbayern
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 80,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. Our HPCS (High Performance Chromatography Solutions) products and solutions support our customers to solve critical issues across many market segments such as pharmaceuticals, food safety, environmental, clinical, and research. Our goal is to provide integrated products and workflow solutions across our instruments, software, and consumables to our customers working to make the world healthier, cleaner, and safer. With more than 1000 employees across the globe maintaining our intense focus on innovation and customers, the HPCS businesses have a bright future. Join our Product Support Engineering team as  Product Support Specialist (f/m/d)As Product Support Specialist you will facilitate and execute post sales actions and initiatives aimed to drive customer satisfaction by troubleshooting and solving customers’ challenges for the Thermo Scientific HPLC and consumable business. Further, you will have responsibility for product quality by sharing the field experience with cross functional teams to identify and drive improvements. Your feedback is key to share customer experience within new product development projects in collaboration with sales, quality, support and marketing partners globally. What you will do   Deliver international support to our customers to troubleshoot issues, optimize methods, and resolve technical problems Investigate reported product failures and perform analysis to determine cause of the problem Efficient communication of field feedback to all relevant departments in order to continuously improve our product quality Responsible for escalation management/participation in escalation Calls Responsible for project work and –management Support the trainings department in training preparation Other miscellaneous duties as assigned Education   Bachelor’s degree required, preferably in chemistry or life sciences Master’s or related advanced degree beneficial Experience Profound experience in application development and/or field service within pharmaceutical or food analysis segment, or related experience GC and LC equipment and lab experience, ideally in combination with MS beneficial   Knowledge, Skills, Abilities Effective in building relationships; a collaborative approach Demonstrated confidence in written, interpersonal and oral communication in English is essential Proactive, independent, assertive, self-starter with the ability to work with a diverse and global team Good project management and leadership skills Affinity to technical contexts, combined with strong critical thinking and problem solving capabilities Ability to prioritize, and work in a dynamic and evolving environment Willingness to travel and work global hours as required Employment within an innovative, growth-oriented organization. Outstanding career and development prospects. Company pension scheme and other fringe benefits. Exciting company culture, which stands for integrity, intensity, involvement and innovation.
Zum Stellenangebot

Medical Solution Manager (m/f/x)

Di. 15.06.2021
München
Are you passionate to digitalize the healthcare world of Carl Zeiss Meditec AG as part of our digital business unit team? As an expert on regulatory and clinical affairs you will be in the driver’s seat to boost our ecosystem from strategy to launch. We are looking for a Medical Solution Manager with broad experience shaping medical products from concept to product launch. In addition, you will peer up with other Medical Solution Managers and Program Managers to shape an agile ecosystem that strives for continuous improvement. As regulatory and clinical affairs are key for admitting products worldwide, you will be an essential member of the digital ecosystem of Carl Zeiss Meditec AG. In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.Join us today. Inspire people tomorrow.Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.Apply now! It takes less than 10 minutes. Define regulatory & clinical requirements as part of the product development process for medical products Collaborate with ecosystem leads to create agile processes for medical solutions Engage with product managers to concept and create medical products based on customer needs Build shared service team that supports the health data ecosystem on regulatory & clinical affairs across various levels Steer and maintain documentation processes for medical solutions Status-reporting of regulatory stages to top-management Track and mitigate regulatory and clinical affair risks Medical, science or med-tech related studies or medical documentation apprenticeship background Regulatory affairs and/or clinical affairs experience in the medical device industry An analytical, systematic and goal-oriented approach Prior experience with (scaled) agile program management is a plus An analytical, systematic and goal-oriented approach Team spirit and good communication skills Business fluent in English Wofür wir seit 170 Jahren stehen: Pioniergeist und Bodenhaftung. ZEISS bietet seinen Mitarbeitern ein modernes Arbeitsumfeld, überdurchschnittliche Benefits sowie vielfältige Möglichkeiten zur Weiterentwicklung. Entscheiden Sie Sich für ZEISS. Die verschiedenen Unternehmensbereiche sowie die zentralen Konzern- und Servicefunktionen bei ZEISS bieten zahlreiche berufliche Möglichkeiten für alle Fachrichtungen.
Zum Stellenangebot
123


shopping-portal