Group Data Manager (m/f/d) - Quality Control - temporary
OCTAPHARMA Pharmazeutika Produktionsges.m.b.H.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 until 31.10.2027.
Join us in shaping our vision to provide new health solutions advancing human life.
Your main tasks and responsibilities
- Implementation, optimization and harmonization of workflows and applications on different production sites of Octapharma
- Implementation of innovative new tools and applications for more efficient handling of routine and project processes
- Coordination of activities with relevant stakeholders (other departments / IT / vendors / competence centers)
- Implementation of PowerApps and PowerBI applications in QC departments
- Create and maintain interactive dashboards and reports using data visualization tools for QCs on a global level (e.g. PowerBI)
- Support in software solutions and data integrity concept for QC laboratory related software
- Establishing and maintaining a data governance framework to ensure high data quality, compliance, and effective data management across the organization
Your expertise and ideal skill set
- University degree in bioinformatics or natural sciences with strong IT background (MSc, Phd or equivalent)
- 2-3 years professional experience in pharmaceutical industry especially in the field of quality control (GMP environment) is a plus
- Skilled in using MS Office, PowerApps and PowerBI
- Knowledge of other data warehouse and business intelligence tools (Qlik, Databricks, etc.) advantageous
- Fluent in English (oral and written), German desirable
- Willingness to travel up to 10% (Europe)
- Ability to multitask, high level flexibility and ability to adapt to changing priorities
- Team player with strong problem solving, organizational and time management skills
Your department - where you make an impact
- We, the Group Quality department, are responsible for developing policies and procedures for all CQ Plasma activities based on current applicable regulations, ensuring a standardized approach throughout the organization.
- Our team is divided into CQ Plasma, CQ Control, Corporate Stability Studies, Corporate QC Method Validation, and Corporate 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 4.270,14 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.
Mrs. Johanna Proksch
Octapharma Pharmazeutika Produktionsges.m.b.H.
Oberlaaer Straße 235, 1100 Wien
T: +43 (1) 610 32 4299
You can also reach us Monday to Friday via WhatsApp: +43 (0) 664 88578113
Want to find out more about us?
Visit our website Octapharma Career and follow us daily on LinkedIn.