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Octapharma AG
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  • A leading pharmaceutical company located in Vienna seeks a Summer Inte... mehr ansehen
    A leading pharmaceutical company located in Vienna seeks a Summer Intern for a temporary position in Corporate QC Stability Studies. The internship lasts two months, starting from July. Applicants should have a valid residence and work permit for Austria, a university degree or technical education in chemistry, as well as proficiency in both English and German. The position offers exposure to pharmaceutical production and various beneficial perks, including meal subsidies and training opportunities. #J-18808-Ljbffr weniger ansehen
  • Wählen Sie aus, wie oft (in Tagen) Sie eine Benachrichtigung erhalten... mehr ansehen
    Wählen Sie aus, wie oft (in Tagen) Sie eine Benachrichtigung erhalten möchten: Mitarbeiter (m/w/d) Produktion - pharmazeutische Abfüllung (LVP) Stellen-ID: 62781 Wien, AT Karrierestufe: Einsteiger Fachbereich: Produktion Beschäftigungstyp: Festanstellung Werden Sie Teil einer lebenswichtigen Kette und tragen Sie zu unserem gemeinsamen Ziel bei, das Leben von Menschen zu verbessern. Octapharma ist einer der weltweit größten Hersteller von Arzneimitteln auf Basis von Humanproteinen und entwickelt und produziert Medikamente aus menschlichem Plasma und menschlichen Zelllinien. Wir sind ein privat geführtes Unternehmen, in dem die Wärme einer familiären Atmosphäre mit der Stärke einer globalen Organisation zusammentrifft. Mit rund 1.600 Mitarbeiter:innen ist der Octapharma-Standort in Wien der größte Produktionsstandort und ein erfolgreicher Forschungs- und Entwicklungsstandort. Ihre neuen Tätigkeiten, die Sie begeistern Vorbereitung, Reinigung und Sterilisation von Equipment sowie Raumreinigung Vorbereitung und Sterilisation von Primärpackmitteln Sterile Abfüllung von Infusionslösungen Bedienung von Produktionsanlagen Filtration von Bulklösungen und Probenahmen im Zuge der Produktion Sicherstellung der Einhaltung von GMP-Richtlinien (Good Manufacturing Practice) sowie sorgfältige Dokumentation aller Arbeitsschritte Ihr Profil, das uns überzeugt Abgeschlossene Berufsausbildung (z.B. Lehre) Berufserfahrung in der Pharmabranche von Vorteil (GMP), idealerweise Praxis im sterilen Arbeiten Gutes technisches Verständnis sowie Teamfähigkeit gepaart mit einer genauen und selbstständigen Arbeitsweise Gute Deutschkenntnisse und EDV-Grundkenntnisse Bereitschaft zur Arbeit im 12-Stunden-Schichtbetrieb (Mo-So, Schichten von 06:00–18:00 Uhr und 18:00–06:00 Uhr) mit entsprechenden Freizeitblöcken Vor dem Hintergrund unserer erforderlichen Einschulungszeit suchen wir Personen die langfristig mit uns wachsen möchten Ihre Abteilung, in der Sie etwas bewirken Wir, die Produktion, sind unterteilt in die Fraktionierung (Basisfraktionierung, Feinfraktionierung 1 und 2, Process Support Fractionation) sowie pharmazeutische Produktion (Large & Small Volume Parenterals, Process Support Pharmaceutical Production) sowie Operation Support und Produktionsdokumentation. Unsere Kernaufgaben sind: Auftrennung des Plasmas in Fraktionen, Reinigung und Virusinaktivierung der Plasmafraktionen, Formulierung, Abfüllung und Gefriertrocknung der fertigen Produkte. Mit uns auf Erfolgskurs – was wir Ihnen bieten Betriebsrestaurant & Essenszulage Fachliche & persönliche Weiterbildungsmöglichkeiten Gesundheitsmaßnahmen Kostenloser Parkplatz und Öffi-Ticket Firmenveranstaltungen und Team-Events Alle unsere attraktiven Benefits auf einen Blick: Benefits Ihr KV-Mindestbruttogehalt (chemische Industrie) beträgt EUR 2.797,95 für 38 Wochenstunden (Vollzeit). Da wir bestrebt sind, Ihr Gehalt individuell an Ihr Profil und Ihre Qualifikationen anzupassen, besteht die Bereitschaft zur Überzahlung. Es liegt uns im Blut Wir leben Vielfalt und stehen als Arbeitgeber für Chancengleichheit! Daher freuen wir uns auf Ihre Bewerbung über unsere Karriereseite - unabhängig von Alter, Geschlecht, Herkunft, sexueller Orientierung und Religion. Haben Sie noch Fragen? Dann kontaktieren Sie Ihre Ansprechperson. Stephanie Pistauer, BA MSc Octapharma Pharmazeutika Produktionsges.m.b.H. Oberlaaer Straße 235, 1100 Wien T: +43 (1) 610 32 - 1308 Octapharma ist eines der weltweit größten Unternehmen, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt. Mit mehr als 11.000 Mitarbeitenden unterstützen wir die Behandlung von Patientinnen und Patienten in 120 Ländern mit Produkten in drei therapeutischen Bereichen: Immuntherapie, Hämatologie und Intensivmedizin. Mit sieben Forschungs- und Entwicklungsstandorten sowie fünf hochmodernen Produktionsstätten in Österreich, Frankreich, Deutschland und Schweden betreibt Octapharma zudem über 195 Plasmaspendezentren in Europa und den USA. Seit vier Jahrzehnten engagieren wir uns für die kontinuierliche Verbesserung der Versorgung von Patientinnen und Patienten weltweit. #J-18808-Ljbffr weniger ansehen
  • A global pharmaceutical company is seeking a Summer Intern in Corporat... mehr ansehen
    A global pharmaceutical company is seeking a Summer Intern in Corporate QC Method Validation in Vienna, Austria. This entry-level temporary position is ideal for students with a scientific background and offers valuable insights into pharmaceutical production. Responsibilities include supporting documentation and various administrative tasks. Applicants must be fluent in English, possess valid hepatitis vaccinations, and hold a work permit for Austria. The internship offers benefits like meal subsidies, training, and a gross salary of EUR 2,010.75 for full-time hours. #J-18808-Ljbffr weniger ansehen
  • Summer Intern (m/f/d) - Corporate QC Method Validation - temporary Jo... mehr ansehen
    Summer Intern (m/f/d) - Corporate QC Method Validation - temporary Job ID: 62180 Location: Wien, AT Job Level: Entry Level Job Category: Quality Employment Type: Temporary employment Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation. With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. This position is temporary from 01.07.2026 until 31.08.2026 (2 months) or from 01.08.2026 until 30.09.2026 (2 months) with 38 hours per week. We look forward to receiving your application. Please upload the following application documents : cover letter stating your desired period of employment , CV, and your high school diploma or degree certificate and a current transcript of your academic achievements. Your main tasks and responsibilities This internship is designed to complement your training and give you an insight into the work and activities of a pharmaceutical production company Supporting documentation & improvement within the department Diverse administrative tasks within the cQC Method Validation department Your expertise and ideal skill set Students with a scientific background Fluency in English Interest in analytics Valid vaccination protection against hepatitis A and hepatitis B Valid residence and work permit for Austria Good skills in Microsoft Office (Word, Excel, Power Point) Sense of responsibility, flexibility and ability to work in a team Organizational talent, multi-tasking and accurate way of working Your department - where you make an impact We, the Corporate Quality department, are responsible for the development of policies and procedures for all CQ Plasma activities based on current applicable regulations to ensure a standardized approach throughout the organization. We are divided into CQ Plasma, CQ Control, Corp. Stability Studies, Corp. QC Method Validation and Corp. QC Incoming Goods. Thrive with us Company restaurant & meal subsidy Training & further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits! You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 2,010.75 (with high school diploma and/or over 18 years of age) based on 38 hours per week (full-time). It´s in our blood We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion. Do you have any questions? Then get in touch with your contact person. Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. #J-18808-Ljbffr weniger ansehen
  • Summer Intern (m/f/d) - Corporate QC Stability Studies - temporary Job... mehr ansehen
    Summer Intern (m/f/d) - Corporate QC Stability Studies - temporary Job ID: 62366 Location: Wien, AT Job Level: Entry Level Job Category: Quality Employment Type: Temporary employment Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately‑owned company, where the warmth of family meets the scale of a global organisation. With over 1600 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. This position is available on a temporary basis for a period of two months between 01.07.2026 and 30.09.2026 . There is also the option to complete a one‑month internship within this timeframe. We look forward to receiving your application. Please upload the following application documents : cover letter stating your desired period of employment , CV, and, for high school students, your 2026 mid‑year report or, for university students, your high school diploma or degree certificate and a current transcript of your academic achievements. Your main tasks and responsibilities This internship is designed to complement your training and give you an insight into the work and activities of a pharmaceutical production company Supporting documentation & improvement within the department Assisting a corporate team in organizing and conducting stability studies Your expertise and ideal skill set Scientific education (university degree, technical college, chemistry HTL) Advanced proficiency in English and German Valid residence and work permit for Austria Accurate and precise working style Your department - where you make an impact We, the Corporate Quality department, are responsible for the development of policies and procedures for all CQ Plasma activities based on current applicable regulations to ensure a standardized approach throughout the organization. We are divided into CQ Plasma, CQ Control, Corp. Stability Studies, Corp. QC Method Validation and Corp. QC Incoming Goods. Thrive with us Company restaurant & meal subsidy Training & further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits! You can find all offers here: Benefits The minimum gross salary according to the collective agreement (chemical industry) is EUR 1,616.51 (without high school diploma and under 18 years of age) / EUR 2,010.75 (with high school diploma and/or over 18 years of age) based on 38 hours per week (full‑time). It´s in our blood We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion. Do you have any questions? Then get in touch with your contact person. Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state‑of‑the‑art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. #J-18808-Ljbffr weniger ansehen
  • Ein führender Anbieter von Arzneimitteln in Wien sucht einen Mitarbeit... mehr ansehen
    Ein führender Anbieter von Arzneimitteln in Wien sucht einen Mitarbeiter (m/w/d) in der Produktion für die pharmazeutische Abfüllung. In dieser Rolle sind Sie verantwortlich für die Reinigung und Sterilisation von Produktionsequipment sowie die Abfüllung von Infusionslösungen. Der ideale Kandidat hat eine abgeschlossene Berufsausbildung und idealerweise Erfahrung in der Pharmabranche. Attraktive Benefits sowie die Möglichkeit zur individuellen Gehaltserhöhung werden angeboten. #J-18808-Ljbffr weniger ansehen
  • Ein globaler Hersteller von Arzneimitteln sucht einen Mitarbeiter für... mehr ansehen
    Ein globaler Hersteller von Arzneimitteln sucht einen Mitarbeiter für die Kreditorenbuchhaltung. In dieser Position sind Sie verantwortlich für die Verbuchung von Eingangsrechnungen und die Wartung der Lieferantenstammdaten. Sie bringen eine abgeschlossene kaufmännische Ausbildung mit sowie fließende Deutsch- und sehr gute Englischkenntnisse mit. Vorteile wie ein Betriebsrestaurant, Weiterbildungsmöglichkeiten und Gesundheitsmaßnahmen werden geboten. Der Standort ist in Wien. #J-18808-Ljbffr weniger ansehen
  • Ein führender Pharmakonzern in Wien sucht einen motivierten Mitarbeite... mehr ansehen
    Ein führender Pharmakonzern in Wien sucht einen motivierten Mitarbeiter im Bereich Quality Assurance. Ihre Aufgaben umfassen die Chargendokumentation und die Sicherstellung der Produktqualität durch die Überprüfung und Freigabe von Arzneimitteln. Kandidaten sollten ein naturwissenschaftliches Studium oder eine Ausbildung im Bereich Chemie besitzen und fließende Deutschkenntnisse sowie sehr gute Englischkenntnisse mitbringen. Wir bieten ein attraktives Gehalt und tolle Benefits. #J-18808-Ljbffr weniger ansehen
  • A leading human protein manufacturer, located in Vienna, seeks a Group... mehr ansehen
    A leading human protein manufacturer, located in Vienna, seeks a Group Lead Automation & Process Engineer. This role involves providing technical leadership for greenfield production facilities, aligning engineering strategies for efficiency, and driving innovation in processes. Candidates should possess a Master's degree in a relevant engineering discipline and have over 15 years of experience in engineering. This position provides a chance to shape the future of manufacturing with a competitive salary and benefits package. #J-18808-Ljbffr weniger ansehen
  • Select how often (in days) to receive an alert: Overview Group Lead A... mehr ansehen
    Select how often (in days) to receive an alert: Overview Group Lead Automation & Process Engineer (m/f/d) - Technical Unit Job ID: 61707 Location: Wien, AT Job Level: Management Job Category: Technical Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation. As a Group Lead Automation & Process Engineering , you will provide technical leadership in the development and industrialisation of Octapharma’s next-generation greenfield production facilities. You will steer automation and process engineering disciplines across major international investment projects, ensuring that new manufacturing sites are designed, built and commissioned to deliver compliant, scalable and sustainable routine production from day one. By establishing global standards and forward-looking technical solutions, you will shape the foundation of our future manufacturing network. The position will be filled in Vienna (Austria), Springe (Germany), Stockholm (Sweden) or Lingolsheim (France). Join us in shaping our vision of providing new health solutions advancing human life. Your main tasks and responsibilities Define and align the engineering strategy with corporate functions and HcEng to ensure capacity, efficiency, and operational readiness for a greenfield plant project Act as overall engineering lead for the development project; define standard equipment requirements and lead the review and challenge of investment plans in line with company strategy and business risk considerations Capture and document critical knowledge to enable successful Manufacturing, Science and Technology (MSAT) transfer; align site structures and staffing, ensure global capacity planning timelines, and drive technical standardization across production lines to enable cross-site learning and training Monitor emerging engineering methodologies and technologies to drive process improvements for the new plant, and strengthen collaboration across engineering groups to share expertise and best practices Define the required level of engineering standardization and implementation priorities; identify best practices with HcEng and sites, establish standard requirements for the project, and develop a roadmap for rollout Ensure adherence to all relevant safety and quality regulations and standards; provide technical leadership for development and production teams at the new site, and mentor and support junior engineers Oversee the functional budget, ensuring cost-effectiveness and financial control Your expertise and ideal skill set Master degree in Automation Engineering, Process Engineering, Chemical Engineering or a comparable technical discipline 15+ years of broad and in-depth engineering experience, including implementation of new processes, preferably within the pharmaceutical industry Proven leadership experience in cross-functional environments, including responsibility for engineering activities within large-scale investment projects Strong expertise in process control strategies and automation architectures Solid understanding of GMP and pharmaceutical regulatory requirements Strategic mindset combined with hands-on technical expertise, strong curiosity, and a passion for driving innovation High level of ownership, accountability and solution orientation, paired with strong communication and stakeholder management skills Willingness to travel up to 30% You will thrive in this role if you are a forward-thinking leader who combines technical excellence with global collaboration, driving future-ready automation solutions that shape the next generation of manufacturing. Your department - where you make an impact The Group Technical Organization consists of Group Engineering, Automation, and Maintenance. We are represented at all production sites in Europe. You will work in a multinational organization supporting all production sites from a technical perspective. The Engineering department mainly works on project development in the early phases of strategic projects. Thrive with us You help save lives - Every day is meaningful as we produce life-saving medicines Family values - Long-term perspective for employees and relationships Be rewarded with an attractive salary and benefits package You will have a high level of influence where you can make a difference and leave your footprint Work with skilled and fun colleagues in a relatively informal organization Skills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions Additional information (Austria only): The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.686,11 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary. It´s in our blood We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion. Do you have any questions? Then get in touch with your contact person. Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. #J-18808-Ljbffr weniger ansehen

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