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Pharmazie: 21 Jobs in Oberhaching bei München

Berufsfeld
  • Pharmazie
Branche
  • Pharmaindustrie 16
  • Groß- & Einzelhandel 1
  • Medizintechnik 1
  • Recht 1
  • Sonstiges Produzierendes Gewerbe 1
  • Unternehmensberatg. 1
  • Verkauf und Handel 1
  • Wirtschaftsprüfg. 1
  • Wissenschaft & Forschung 1
Berufserfahrung
  • Mit Berufserfahrung 18
  • Ohne Berufserfahrung 10
  • Mit Personalverantwortung 2
Arbeitszeit
  • Vollzeit 19
  • Teilzeit 2
  • Home Office 1
Anstellungsart
  • Feste Anstellung 18
  • Praktikum 2
  • Berufseinstieg/Trainee 1
Pharmazie

Mitarbeiter für den Bereich Pharmakologie (m/w/d) mit Schnittstelle zum Bereich Qualitätssicherung

Mo. 02.08.2021
Puchheim, Oberbayern
Die OmniVision GmbH ist ein expandierendes mittelständisches Unternehmen in der Augenheilkunde mit Hauptstandort in Deutschland sowie Standorten in Österreich, der Schweiz und Italien. In Deutschland gehört die OmniVision GmbH zu den führenden nicht-konzerngebundenen ophthalmologischen Unternehmen. Unser Produktportfolio umfasst Arzneimittel, Medizinprodukte und Nahrungsergänzungsmittel. Im Zuge unseres starken Wachstums suchen wir zum nächstmöglichen Zeitpunkt für unseren Hauptstandort in Puchheim bei München einen engagierten und motivierten: Mitarbeiter im Bereich Pharmakovigilanz mit Schnittstelle zum Bereich Qualitätssicherung (m/w/d) Eigenständige Planung und Erstellung von Pharmakovigilanz-Dokumenten (z.B. PSUR, RMP, PV Verträge) Wissenschaftliche Bewertung und Bearbeitung von Literaturfällen und Spontanmeldungen (z.B. Nebenwirkungsmeldungen für Arzneimittel und Medizinprodukte) Pflege der Pharmakovigilanz-Datenbank Ansprechpartner (m/w/d) für andere Abteilungen bezüglich Anfragen zur Pharmakovigilanz von Arzneimitteln und Medizinprodukten Erstellung und Pflege relevanter Pharmakovigilanz-SOPs Kommunikation mit den zuständigen Behörden und Benannten Stellen Implementierung und Optimierung der Prozesse Unterstützung bei der Bearbeitung und Bewertung von technischen Reklamationen zu allen Produktgruppen Abgeschlossenes Hochschulstudium mit naturwissenschaftlichem Schwerpunkt oder Ausbildung als PTA, MTA, BTA oder vergleichbar Mehrjährige Berufserfahrung  im Bereich Pharmakovigilanz oder Qualitätssicherung Sehr gute Englischkenntnisse in Wort und Schrift Sehr gute MS Office-Kenntnisse Selbstständige und strukturierte Arbeitsweise Zuverlässigkeit, Engagement sowie Sorgfalt und Detailtreue Zeitliche Flexibilität, Belastbarkeit Teamorientierung Eine unbefristete, langfristig orientierte Festanstellung in einem erfolgreichen, inhabergeführten mittelständischen Unternehmen der Pharmabranche Ein wachsendes, professionelles Team, das mit Leidenschaft den Wachstumskurs unseres Unternehmens mitgestaltet Selbstständiges Arbeiten in flachen Hierarchien mit kurzen Entscheidungswegen Ein attraktives und leistungsorientiertes Gehalt sowie flexible Arbeitszeiten Sehr gute Weiterbildungsmöglichkeiten sowie modernes IT-Equipment runden unser Angebot ab
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Project Manager GMP Production (m/f/d)

Sa. 31.07.2021
Ebersberg
We are fascinated about the power of DNA and how it is incorporated in everything we do, work and live. Being passionate about our strong customer orientation, our service and our quality standards, we continuously challenge ourselves to stay ahead and remain one of the leading genomics service providers worldwide. Eurofins Genomics is globally known for its innovative and customised technologies in the life science industries and academic research institutions. A career at Eurofins Genomics is the opportunity to translate your career plans and dreams into reality. We offer you not only the chance to develop a successful career - we offer you the opportunity to make a difference in the world of the four bases. For our Oligo & Genesynthesis Team in Ebersberg (close to Munich) we are looking as soon as possible for a Project Manager GMP Production (m/f/d). Devolop your creative drive and build a solid foundation for this new production area with full responsibility Improve all details of this facility to get the best out of the given opportunity Lead and develop the oligonucleotide GMP production Team in Ebersberg Report directly to the Managing Director of the oligonucleotide synthesis Structure the production in order to fulfill existing client needs Ensure all GMP requirements are present and regularly updated Communicate regular department updates to the management, peers and to the staff in the lab Steer the sales team with recent updates on capabilities and market insights Help others to succeed in their daily challenges Support the entire company with you people skills ensuring the strong company growth is managed effectively Your profile: You are passionate about oligonucleotides, GMP and people You master the daily challenge of incremental changes to fill the mosaic instead of always aiming for the next big thing You proudly own a master or PhD in the areas of Biology, Chemistry or Business You look back on a proven track record in production for oligonucleotide synthesis, solid phase DNA synthesis or peptide synthesis You lead by example and your energy motivates your colleagues and business partner Your curious mind fluently thinks and expresses itself in English and German You structure the plans and the execution always with the key result in mind You enjoy representing the team and rather help others to shine than focusing yourself on nitty gritty details We are a leading European BioTech services company are part of one of the world's largest analytical services companies (> 50.000 employees and 4bn in sales) are highly decentral organization granting immense freedom and asking to take full responsibility for actions have the thinking, speed, drive for excellence and the precision of ex-McK consultants without the 200-page ppt and overhead
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Praktikum M&A (m/f/d)

Fr. 30.07.2021
München
Adragos ist der global operierende Investment Arm eines Deutschen Family Offices. Wir investieren ausschließlich außerhalb der Kapitalmärkten und erwerben immer 100% der Unnternehmensanteile. Echte Wertschöpfung erfordert ein tiefes Verständnis der Branche, in der man tätig ist. Aus diesem Grund konzentrieren wir uns ausschließlich auf den Pharma-Sektor. Unser Schwerpunkt liegt dabei auf so genannten CDMOs (Contract Development and Manufacturing Organisations), Zulieferern für die Pharmaindustrie, welche in Europa und Nordamerika angesiedelt sind. Wir glauben nicht an über-ambitionierte, aggressive Transformationen, sondern an eine langfristige, nachhaltige Wertschöpfung. Wir bauen Unternehmen auf, die einen substantiellen Wert für unsere Gesundheitssysteme darstellen. Wir restrukturieren keine defizitären Assets, sondern investieren in risikoarme Geschäftsbereiche hochwertiger, unterbewerteter Unternehmen. Wir suchen ab sofort Unterstützung für 3-6 Monate: Du schaffst einen M&A-Funnel, den sogenannten Deal Flow Du unterstützt das Team bei Commercial und Financial DDs Du designst Pitch-Decks und bereitest Investorentreffen und Ähnliches vor Du konzipierst und führst Markt- und Unternehmensanalysen durch, pflegst und konzipierst Finanzmodelle Du studierst Naturwissenschaften oder Betriebswirtschaft und interessierst dich für die pharmazeutische Industrie Du besitzt Microsoft Powerpoint und Excel-Know-how sowie eine gute Portion gesunden Menschenverstand Vorkenntnisse aus den Bereichen Beratung, Marketing, Sales, Brand Management sind erwünscht (z.B. Praktika bei großen Beratungsfirmen oder Boutiquen) Unser Team ist klein und sehr ambitioniert - du wirst von Tag 1 wie ein vollwertiges Teammitglied behandelt und übernimmst vom ersten Tag an verantwortungsvolle Aufgaben Du arbeitest eng mit unseren Partnern und unserem Team zusammen und wirst voll in das Tagesgeschehen eines Pharma-Unternehmens eingebunden Wir garantieren dir eine steile Lernkurve und spannende Aufgaben! Da wir ein modernes Unternehmen sind, haben wir eine unternehmerische und informelle Atmosphäre, natürlich mit kostenlosem Kaffee und Obst und gelegentlichem After-Work-Drink
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Scientist (w/m/d) Drug Product Development for Biopharmaceuticals

Fr. 30.07.2021
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. 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.
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Medical Solution Manager (m/f/x)

Fr. 30.07.2021
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.
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Junior Scientist (m/w/d) – Biopharmaceutical Analytics

Fr. 30.07.2021
Planegg
Coriolis Pharma is a globally operating independent service provider for formulation research and development of for a large variety of different (bio)pharmaceutical molecules, including proteins, peptides, nucleic acids, ATMPs, GMOs, vaccines and virus(-like) particles. 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. At our company, we pursue one goal every day: the advancement of medicines to cure people. Our expanding company currently employs about 140 people at two sites.Scientific Work: Apply expert knowledge and perform analytical analysis and data interpretation of biological molecules (proteins, peptides, viruses, etc.) Take over responsibility for analytical instruments and methods including biophysical characterization of biopharmaceuticals. Be or develop towards a scientific expert on multiple analytical methods, including Analytical Ultracentrifugation, structural analysis, (sub-)visible particle testing and Pharmacopoeial methods for the characterization of biological molecules Perform data analysis using our own data processing server for SEDFIT or UltraScan ensuring highest quality standards Provide internal scientific consulting for analytical systems to Coriolis Scientists Be a trendsetter, drive innovation and further strengthen our analytical expertise Project Management: Perform analytical service for our clients and make sure that clients’ needs are met Coordinate teams as (deputy) project leader to reach the defined objectives Ensure that projects are executed with highest quality within given timelines and budget Be the interface to other internal and external stakeholders (e.g. scientific board, business development, service providers) University degree in biotechnology, pharmacy, pharmaceutical sciences, (bio)chemistry, chemical engineering, biology or related field Strong analytical background, with high affinity for instrumental analytics Experience in the field of Biopharmaceutical Analytics (.e.g chromatography, electrophoresis, spectroscopy) Team player with strong motivation, inter-personal skills and excellent communication abilities in English As Junior Scientist (m/w/d) you are - together with the project team - responsible for the successful execution of research and development projects for our customers worldwide.We offer you diversified and challenging areas of responsibilities in our innovative company. 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.
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Junior Scientist (m/w/d) Protein Liquid Formulation and/or Lyophilization Development

Fr. 30.07.2021
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.As 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.
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Junior Regulatory Affairs Manager (m/w/d)

Mi. 28.07.2021
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. 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. Zur Unterstützung unseres Teams suchen wir zum nächstmöglichen Zeitpunkt einen Junior Regulatory Affairs Manager (m/w/d)In dieser Position sind Sie verantwortlich für die Koordination und Durchführung von zulassungsrelevanten Aufgaben für die Ihnen zugeordneten Produkte für den deutschen Markt. Zu Ihren Hauptaufgaben zählen: 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 1-2 Jahre Berufserfahrung im Bereich Arzneimittelzulassung 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
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Junior Scientist (m/w/d) – Cell culture, viral vectors and cell/virus -based ATMPS

Mi. 28.07.2021
Planegg
Coriolis Pharma is a globally operating independent service provider for formulation research and development of for a large variety of different (bio)pharmaceutical molecules, including proteins, peptides, nucleic acids, ATMPs, GMOs, vaccines and virus(-like) particles. 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. At our company, we pursue one goal every day: the advancement of medicines to cure people. Our expanding company currently employs about 140 people at two sites.As 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 in formulation development projects for virus-based advanced therapy medicinal products (ATMPs), including liquid and/or freeze-dried (pre)formulation studies, stability studies and stress testing of virus formulations Support project teams in analytical characterization of viruses, viral vectors and vaccines from nanometer to the visible size range by using cutting edge technology (e.g. dynamic light scattering, micro-flow imaging, nanoparticle tracking analysis, TEM, cell-based assays…) Plan and perform routine cell culture work and cell-based assays to quantify biological activity of viruses (e.g. TCID50, plaque assay) Perform data analysis and support 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 Life Sciences (virology, biotechnology, pharmacy, (bio)chemistry, chemical engineering, biology etc.) Experience in the fields of cell culture and work with viruses, viral vectors and vaccines Experience in working under biosafety level 2 (BSL2) Team player with strong motivation, inter-personal skills and excellent communication abilities (English is a must) 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.
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Postdoctoral Scientist (m/w/d) Formulation and characterization of virus-based ATMPs

Mi. 28.07.2021
Planegg
Coriolis Pharma is a globally operating independent service provider for formulation research and development of for a large variety of different (bio)pharmaceutical molecules, including proteins, peptides, nucleic acids, advanced medicinal therapeutics (ATMPs), genetically modified organisms (GMOs), vaccines and virus(-like) particles. 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. At our company, we pursue one goal every day: the advancement of medicines to cure people. Our expanding company currently employs about 140 people at two sites.As a Postdoctoral Scientist you will work on the following tasks: Conduct research in the field of formulation and characterization for virus-based advanced therapy medicinal products (ATMPs), including liquid and freeze-dried formulation studies, stability studies and stress testing of virus formulations Establish protocols and perform analytical characterization of viruses, viral vectors and vaccines from nanometer to the visible size range by using cutting edge technology, e.g. dynamic light scattering (DLS), transmission electron microscopy (TEM), flow imaging microscopy, analytical ultracentrifugation and other methods Establish protocols and perform cell-based assays to quantify biological activity of viruses (e.g. TCID50, plaque assay) Establish protocols and perform Real-time PCR (qPCR) assays to quantify physical virus titers Project planning, project coordination, experimental work (evaluation and implementation of analytical methods), reporting, and communication within the project team Generate scientific output of the project (publications, posters, presentations) and participation at international conferences Be a trendsetter, drive innovation and further strengthen our analytical expertise with focus on virus formulations PhD degree in Life Sciences (virology, biotechnology, pharmacy, pharmaceutical sciences, (bio)chemistry, immunology, or related field) Strong background and profound knowledge in virology, and/or the field of ATMPs, and/or work with viruses, viral vectors and vaccines are mandatory Experience in working under biosafety level 2 (BSL2) Experience in particle characterization and/or handling of cells is a plus High interest in scientific work on a pharmaceutically relevant topic performed in a collaborative setting Ability for critical thinking and implementation of scientific ideas into practice 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 Postdoctoral 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 and the realization of your own ideas, i.e. specialization on management or scientific tasks. Beyond that Coriolis offers a variety of benefits and team activities to its employees.
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