Job ID: 63835
Location:
Wien, AT
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Job Level: Entry Level
Job Category: Quality
Employment Type: Temporary employment
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 (Junior) Expert Validation - LIMS, you will help ensure inspection-ready CSV documentation and end-to-end traceability for the octaLIMS program while supporting ongoing validation activities.
This is a temporary position, starting as soon as possible and running until 31 August 2027.
Join us in shaping our vision of providing new health solutions advancing human life.
Your main tasks and responsibilities
Review, update and structure the Excel-based traceability matrix, including document references, versions, releases and other relevant information
Ensure end-to-end traceability across validation documentation and identify missing or incomplete information
Work closely with colleagues and subject matter experts to gather relevant information
Maintain compliant CSV documentation and support validation-related CAPAs and inspection preparation
Support validation activities, including Operational Qualification and the management of discrepancies arising from validation testing
Your expertise and ideal skill set
Degree in Life Sciences, Computer Science, Engineering or a related field
First experience in the pharmaceutical or another regulated industry is an advantage; graduates are also welcome to apply
Familiarity of Computer System Validation principles (e.g. GAMP 5) is beneficial
Knowledge of LIMS and document management systems, such as Veeva Vault, is a plus
Very good Microsoft Office skills, particularly Excel, and the ability to structure and manage complex information in a clear and detail-oriented way
Strong English communication skills and the confidence to approach colleagues, gather information and follow up on open topics
Your department - where you make an impact
We, the Group Quality department, are responsible for the development of policies and procedures for all GQ Plasma activities based on current applicable regulations to ensure a standardized approach throughout the organization.
We are divided into GQ Plasma, GQ Control, Group Quality Assurance, Group Stability Studies, Group QC Method Validation, Group QC Incoming Goods and Group Quality & Compliance Projects.
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 3,463.06 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.
Larissa Amling
Octapharma Pharmazeutika Produktionsges.m.b.H.
Oberlaaer Straße 235, 1100 Wien
T: +43 664 789 53 728
Want to find out more about us?
Visit our website Octapharma Career and follow us daily on LinkedIn.
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About Octapharma
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.
