Director Quality Assurance (m / f / d)

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Octapharma specializes in the development of highly pure pharmaceuticals made from human blood plasma. As part of a family-owned enterprise, Octapharma in Vienna is not only the largest production site but also a successful research location within the Octapharma Group. Due to our continued growth, we are now hiring for our team :

Your new challenges which will inspire you :

• Lead the Clinical Quality Assurance team, define tasks and responsibilities, and oversee Clinical Quality Assurance activities.
• Ensure clinical trials are conducted in compliance with applicable regulations and guidelines.
• Provide compliance advice to operational units.
• Ensure all clinical documentation complies with regulations and guidelines.
• Support the preparation, conduct, and follow-up of regulatory inspections of clinical studies.
• Act as the interface between Octapharma’s Corporate Quality Assurance and global Clinical R&D teams.

Your profile that will convince us :

25%.

Additional information :

The minimum gross wage according to the collective agreement (chemical industry) for this position is EUR 5,598.85. We aim to adjust your salary based on your responsibilities and profile, and are willing to pay above the collective agreement wages.

We look forward to new, committed employees who will help us continue our strong growth and enable patients to live better lives — because it is in our blood! We encourage you to apply via our online career portal.

Your contact : About Octapharma

Octapharma is one of the world's largest human protein manufacturers, developing and producing proteins from human plasma and cell lines. We employ over 11,000 people worldwide, supporting patient treatment in 120 countries across three therapeutic areas : Immunotherapy, Hematology, and Critical Care. With seven R&D sites and five manufacturing facilities in Austria, France, Germany, and Sweden, and over 195 plasma donation centers across Europe and the US, we are committed to advancing patient care globally.

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