Group Expert - Quality Management IT - Track & Trace

• Drive and support IT Quality Management and manage all IT Compliance aspects
• Manage the validation of computerized systems
• Support and oversee all IT changes and projects
• Act as a Business Partner to IT
• Write and train GxP documents
• Support software lifecycle and planning
• Improve and maintain the Quality Framework within the department
• Collaborate with cross-functional teams and international partners, * Our primary mission is to support production by providing scientific and technical expertise, optimizing processes, and ensuring that manufacturing runs efficiently, safely, and in compliance with regulatory requirements.
• We, the Manufacturing Science and Technology department, are structured into the following areas: Group Active Pharmaceutical Ingredient Production, Group Fill & Finish, Group Manufacturing Intelligence, Group Pilot Production, Group Process Qualification & Validation and Group Material Qualification.

• University degree in a relevant field
• At least 2 years of pharmaceutical industry experience, ideally with an IT compliance focus
• Practical experience with track & trace is beneficial.
• Proficient in English; German, French or Swedish is a plus
• Goal-oriented and hands-on, with a high level of self-responsibility and a strong focus on quality and efficiency

• 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 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.

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.

As Group Expert - Quality Management IT within the MSAT / Track & Trace team, you will play a key role in managing IT compliance across this area. You will provide expert guidance and support projects and changes within the Track & Trace / MSAT environment. Working closely with our IT teams, you will also act as a Business Partner to IT. Ensuring the required quality of our continuously evolving IT systems will be a key focus of this role.

Join us in shaping our vision of providing new health solutions advancing human life., Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing plasma-derived and recombinant medicines. Octapharma employs more than 11,000 people worldwide to support the treatment of patients in 120 countries with products in three therapeutic areas: Immunotherapy, Haematology, and Critical Care. Octapharma has seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany and Sweden, and operates more than 200 plasma donation centres across Europe and the US., Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Strasse 235 1100 Wien Arbeitgeberprofil ansehen