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biotechnologie: 4 Jobs in Dreieich

  • biotechnologie
  • Pharmaindustrie 3
  • Medizintechnik 1
  • Bad Homburg 2
  • Darmstadt 1
  • Frankfurt am Main 1
  • Leverkusen 1
  • Ulm (Donau) 1
  • Mit Berufserfahrung 4
  • Ohne Berufserfahrung 1
  • Vollzeit 4
  • Feste Anstellung 3
  • Befristeter Vertrag 1

Senior Scientist (all genders), Advanced Cell Culture Technologies (limited to 18 months)

Mi. 12.02.2020
A career at our company is an ongoing journey of discovery: our around 56,000 people are shaping how the world lives, works and plays through next generation advancements in healthcare, life science and performance materials. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. Senior Scientist, Advanced Cell Culture Technologies (limited to 18 months)  The Advanced Cell Culture Technology team focuses on understanding the chemistry of cell culture media and developing new cell culture media components. We are currently seeking a highly motivated and innovative Senior Scientist who will apply his scientific knowledge and leadership to advance the current understanding behind cell culture media. The successful candidate will: Design, develop and optimize new products and strategies for biopharmaceutical applications. Implement new cutting-edge technologies in the field of biology, chemistry or analytics Lead junior scientists in the design, execution and interpretation of scientific experiments. Be responsibility for lab infrastructure, instrument maintenance, documentation and qualification. Maintains proactive role in sales and marketing support. Establish and maintain collaborations with other departments or universities. Write comprehensive scientific reports, patent applications and scientific publications Who you are min. PhD chemistry, biochemistry or biological Sciences, with a focus in biotechnology with 4-5 years of experience Experience in mammalian cell/tissue culture techniques Experience with microbioreactors cell culture screening system and metabolic analyses using advanced analytical methods. Experience with robotics, high-throughput cell culture techniques as well as cutting edge analytics (metabolomics, transcriptomics …) Ability to apply statistical designs, perform statistical analysis and use MVDA to analyze highly complex datasets. Strong skills in critical thinking, laboratory experimentation and data analysis. Ability to multitask and maintain organized data systems. Ability to work independently Strong communication and interpersonal skills to work in team environment Fluency in English (oral & written). German is a plus    What we offer:  With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life! Curious? Apply and find more information at
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(Senior) Scientist/Manager Process Development Regenerative Medicine (m/w/d)

Fr. 07.02.2020
Bad Homburg
/ CAREER WITH A PURPOSE / Fresenius Medical Care - Creating a future worth living. For patients. Worldwide. Every day. More than four decades of experience in dialysis, innovative research, the global leader in dialysis services and products - that is Fresenius Medical Care. About Fresenius Over 270,000 people across the globe work at Fresenius to provide better medicine for more people. Our independent business segments Fresenius Medical Care, Fresenius Kabi, Fresenius Helios and Fresenius Vamed offer a wide spectrum of products and services in the health sector. We offer you the opportunity to make a difference with your career – and to become part of our impressive growth story. Unicyte AG Changing lives. Improving lives. That is our goal, the goal of Unicyte AG. As an independent affiliate of Fresenius Medical Care, we are transformative regenerative medicine company advancing stem cell technologies into a novel class of human therapeutics. Unicyte has translated its ground-breaking discoveries into a broad pipeline in key therapeutic areas. As a pioneer in liver stem cells and nano-extracellular vesicles the company is dedicated to improving the lives of patients with kidney or liver disease, diabetes, and cancer through its three major technology platforms: Our roots lie in a long-term research cooperation between science and industry – just one of the reasons, why we work so fast, precisely and successfully today. Founded in 2015, as an independent subsidiary of Fresenius Medical Care – one of the leading players in the global bioimpedance devices market that plans to invest around 60 million € in Unicyte AG – we strive for a broad therapeutic and patent portfolio. Preferably together with you, of course. You will lead external collaborations (academic and industrial) in the process development of innovative technology platforms with a clear focus on regulatory required data generation. Furthermore, it will be on you to manage our external manufacturing operations with contract manufacturers – from technology transfer to clinical trial supply up to commercial manufacturing. We also rely on your proactive contribution to managing, negotiation and closing of commercial agreements with our contract manufacturers, including pricing and quality agreements. With a trained eye for detail, you will ensure the regulatory compliance of external manufacturing operations – additionally, you will interface with regulatory bodies, in close collaboration with the senior management and external consultants. Developing GMP-relevant documents is also part of your agenda: production protocols, change requests, deviations, user requirement specifications, SOPs etc. Beyond that, you will continuously drive the efficiency of our manufacturing processes across all of our technology platforms and therapeutic programs. Last but not least, you will evaluate and establish process development strategies and tools for stem cells as well as stem cell derived organoids and extracellular vesicles. Successful PhD in Biochemical Engineering, Biotechnology or Biochemistry Minimum 5 years of industrial work experience in pharmaceutical manufacturing and process development of ATMPs and/or biologics – commercial experience is a plus Demonstrable experience with managing third party C(D)MOs Extensive knowledge of taking products from R&D to GMP – including through the upscaling process Versatile knowledge in biologics manufacturing – drug substances and drug products European regulatory experience is a must have, FDA and other regulatory jurisdictions are a plus In-depth know-how of GMP requirements, EH&S regulations, and other regulatory requirements Experience in project controlling and tracking, project management qualification favourable Ideally, basic leadership experience – in any case an empathic and solution-oriented personality with sound communication skills Proven capabilities in working in interdisciplinary and international teams Advantageous: experience in leading R&D oriented academic teams to a strong development mindset Excellent English skills – German and/or Italian skills beneficial Highly motivated self-starter with entrepreneurial spirit, prior start-up experience favourable our corporate culture for “entrepreneurs in an enterprise” where you can quickly take on responsibility. The benefits we offer: Profit-sharing, long-term accounts for your future plans and other benefits which meet individual needs. Working@Global Research & Development (GRD) Our aim in GRD: Global research. We work together with strong partners and start-ups. An inspiring environment awaits you with the freedom that you need. Over 800 colleagues from different disciplines work in international teams. The Bad Homburg site This is where everything comes together – most of the R&D activities take place at our sites in Schweinfurt and Bad Homburg. In Bad Homburg, medical professionals work side-by-side with software specialists, business economists and engineers in interdisciplinary teams to develop new innovations. The company headquarters is also located in Bad Homburg. A total of 3,500 employees work in different companies at the location. Contribute to our work and use your knowledge to improve the quality of life of patients. Thanks to our work, dialysis patients can look to the future with confidence today. The demand for modern dialysis processes is increasing globally – for us, this means that we are growing. Let’s work together: inquisitive and with high demands for quality.
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Mitarbeiter/in GMP-Qualitätskontrolle PCR

Mi. 05.02.2020
Frankfurt am Main
Octapharma Biopharmaceuticals GmbH ist ein 1997 gegründetes, erfolgreich expandierendes Biotechnologie-Unternehmen und eines der Tochterunternehmen der Octapharma AG. Unsere Schwerpunkte sind hochreine, virusinaktivierte Arzneimittel zum Einsatz in den Bereichen Immunologie, Hämophilie und Intensivmedizin. Die Produkte sind im Markt gut etabliert, was sich auch im kontinuierlichen Expansionskurs der Firma widerspiegelt. Mitarbeiter/in GMP-Qualitätskontrolle PCR Virologische Analysen mittels PCR im Routinelabor Arbeiten nach GMP-Richtlinien und standardisierten Arbeitsanleitungen (SOP) Allgemeine Aufgaben zur Labor- und Büroorganisation Erfolgreich abgeschlossene Ausbildung (BTA, CTA, MTA oder vergleichbare Ausbildung) Vorausgesetzt wird mindestens ein Jahr Erfahrung mit Real-Time PCR auf dem Gebiet der Routinediagnostik, idealerweise erworben in einem GxP-Labor Von Vorteil: Kenntnisse über Laborautomation und LIMS Bereitschaft mit standardisierten Methoden zu arbeiten Sehr gute Deutschkenntnisse Freude an der Laborarbeit und Teamgeist sind für die Erfüllung Ihrer Aufgaben ebenso gefragt wie ein hohes Maß an Genauigkeit und Zuverlässigkeit. Ein gutes Betriebsklima in einem beständig wachsenden Unternehmen und in einer modernen „state-of-the-art" Arbeitsumgebung Eine Arbeit, die für die Sicherheit unserer Patienten von größter Bedeutung ist Umfassende Schulung und Einarbeitung in Ihre Aufgaben Eine ihrer Qualifikation entsprechende Vergütung
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Senior Projektingenieure (m/w/d) für unseren Bereich Biotechnologie / API

Mi. 05.02.2020
Bad Homburg, Ulm (Donau), Leverkusen
Für unsere Hauptverwaltung in Bad Homburg und unsere Büros in Ulm, Penzberg und Leverkusen suchen wir zum nächstmöglichen Termin Senior Projektingenieure (m/w/d) für unseren Bereich Biotechnologie / API Leidenschaft für Pharma Engineering. Gegründet und entwickelt von zwei namhaften Pharmaunternehmen, können wir mit Stolz feststellen, dass alle regulatorischen und sonstigen spezifischen Anforderungen dieser Branche Teil unserer DNA sind. Wir sind bestrebt, unsere Dienstleistungen in der Welt der Pharma- und Biotechnologie anzubieten, neu unter der Dachorganisation der TTP AG. Erstmalig 1974 in Deutschland gegründet, folgten Schritt für Schritt Tochtergesellschaften in der Schweiz, Frankreich und Belgien. Heute bedienen wir mit 450 Mitarbeitern an 8 Bürostandorten auf dem europäischen Markt erfolgreich die Bedürfnisse unserer Kunden.Gemeinsam mit einem Team von Ingenieuren und Experten garantieren Sie die optimale Planung von biotechnischen bzw. chemischen Wirkstoffproduktionen und artverwandten Anlagen und sorgen für eine reibungslose Planungs-, Abwicklungs- und Montageorganisation. Zu den vielfältigen Tätigkeiten gehören die selbständige Bearbeitung der Projekte, von der Konzepterstellung über die Anlagenauslegung, der Detailplanung mit Kosten- und Terminplänen, bis zur Auswahl und Betreuung der Lieferanten in der Ausführungsphase. Zum Abschluss der Projekte überwachen Sie die Montage sowie die anschließende Inbetriebnahme. Weiterhin sind Sie der Ansprechpartner für unsere Kunden. Dipl.-Ing. Biotechnologie, Verfahrenstechnik, Pharmatechnik, Maschinenbau oder vergleichbarer Schwerpunkt Mehrjährige Berufserfahrung im pharmazeutischen Anlagenbau/Anlagenplanung, der biotechnischen bzw. chemischen Wirkstoffproduktion bzw. im pharmazeutischen Maschinenbau Kenntnisse im Bereich der Projektierung bzw. Betrieb von Anlagen zur Herstellung von biotechnischen bzw. chemischen Wirkstoffen Kommunikations- und Teamfähigkeit, Eigeninitiative und Einsatzbereitschaft Ein hohes Maß an Flexibilität sowie Mobilität und Bereitschaft zu projektbezogenen Einsätzen vor Ort Gute Deutsch- und Englischkenntnisse in Wort und Schrift Flache Hierarchien – schnelle Aufstiegschancen Flexible Arbeitszeiten Internes Weiterbildungsprogramm Arbeiten in agilen Teams
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