11 geprüfte KI-Jobs in Wien

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The minimum gross salary according to the collective agreement (chemical industry) is EUR 4.355,55 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.

Johanna Proksch, MA Octapharma Pharmazeutika Produktionsges.m.b.H. Oberlaaer Straße 235, 1100 Wien T: +43 (1) 610 32 – 4299 Want to find out more about us? Visit our website Octapharma Career and follow us daily on LinkedIn .

About Octapharma 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 200 plasma donation centres across Europe and the US.

With four decades of experience, we are committed to advancing patient care worldwide. Apply now » Find similar jobs: Global Website Data Privacy Statement Legal Statement Opens in a new tab. Opens in a new tab. © 2026 Octapharma AG × When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies.

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Zur Position

Gehalt: ab EUR 4.355 brutto/Monat 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 1700 employees, the Octapharma site in Vienna is the largest production site, and successful research and development location. Your main tasks and responsibilities Develop and implement the global quality strategy, oversight models and frameworks for Clinical Data Management, Governance, Analytics, Biostatistics, Digital Technologies and AI-enabled systems Provide quality leadership for digital transformation initiatives, e.g. emerging technologies, including machine learning and generative AI applications to ensure data governance, data integrity and quality-by-design principles are embedded in digital processes Drive risk-based analytics to proactively identify and manage quality risks through advanced analytical methodologies and data-driven insights Evaluate AI governance controls, model lifecycle management, training data integrity, explainability, bias mitigation, and change management Provide independent quality assessment of AI use cases in clinical development and operational processes Monitor evolving regulatory expectations related to AI in regulated environments Act as a trusted advisor to Quality, Clinical Development, Data Sciences, Digital Innovation, and Regulatory teams and present Quality Assurance in governance committees and strategic initiatives Mentor QA auditors and quality professionals in digital and AI auditing methodologies Lead and conduct global GxP activities and audits of CROs and technology vendors (Clinical Data Management, Biostatistics and Statistical Programming, Electronic Data Capture (EDC) systems, Clinical databases, AI/ML-enabled platforms, Computerized systems and cloud-based technologies) Your expertise and ideal skill set Completed degree in Life Sciences, Statistics, Computer Science, Data Science, Quality Management, or related discipline At least 10 years of working experience in the Pharmaceutical or CRO Industry Extensive GxP Quality Assurance and auditing experience (e.g. Clinical Data Management, Biostatistics and Statistical Programming, Computerized Systems Validation, Data Integrity) Demonstrated experience assessing AI/ML-enabled systems and digital technologies Experience in supporting FDA, EMA, MHRA and other regulatory inspections Excellent stakeholder management skills with the ability to influence senior internal and external partners Excellent organizational skills, a proactive mindset and the ability to manage multiple strategic priorities Fluent in English, German is a plus (written and oral) Willingness to travel internationally as required Your department – where you make an impact We, the Research & Development unit, conduct preclinical and clinical research to develop new products and ensure their safe and effective use.

Our ultimate focus in our daily work is to enhance patient health and safety. 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: