Group Expert (m/f/d) - Quality Management IT - Track & Trace

JobsinAustria; Wien; Vor Ort; EUR 52.000 - 56.000; Vollzeit

Benefits dieser Stelle

Company restaurant & meal subsidy

Training & further education

Health promotion

Parking spaces and good public transit

Company and team events

Zusammenfassung

Octapharma Pharmazeutika Produktionsges.m.b.H. in Vienna seeks a Group Expert - Quality Management IT to ensure IT compliance across Track & Trace and MSAT. You will partner with IT and drive quality improvements in a global production environment.

You bring a university degree and at least 2 years in pharma IT compliance, with strong English skills and a proactive, quality-focused mindset. The role offers a permanent position at the Vienna site with attractive benefits.

Qualifikationen

• 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.

Aufgaben

• 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

Kenntnisse

Quality mindset

Self-responsibility

Proactive

Ausbildung

University degree in a relevant field

Jobbeschreibung

Job ID: 63998

Location: Wien, AT

Job Level: Entry Level

Job Category: Production

Employment Type: Permanent position

Career Level

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.

Your main tasks and responsibilities

• 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

Your expertise and ideal skill set

• 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

Your department - where you make an impact

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.

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 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.

Contact

Larissa Amling

Octapharma Pharmazeutika Produktionsges.m.b.H.

Oberlaaer Straße 235, 1100 Wien

T: [phone]

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.