Prothya Biosolutions

About the Company

Prothya Biosolutions was formed in 2021, when Plasma Industries Belgium (PIBe), with roots in the Belgian Red Cross, integrated with Sanquin Plasma Products (SPP), a former subsidiary of the Sanquin Blood Supply Foundation (Stichting Sanquin Bloedvoorziening).

Prothya Biosolutions offers over 60 years of experience in the collection of blood plasma and production of plasma-derived medicinal products, and a long legacy of collaboration, innovation, and delivery of science-based solutions.

Thanks to our diverse background, we recognize the unique value of plasma-derived medicinal products for people and society, and reflect this in our ongoing transformation into a results-driven and global organization.

Stable plasma derivatives such as clotting factors, immunoglobulins and albumin solutions are produced with the fractions isolated by Plasma Industries.

At Prothya, we believe the best medicines are already in your body. The human plasma proteome holds the promise of a revolution in disease diagnosis and therapeutic treatment. We will continue to play a leading role in discovering how the abundance and structure of proteins can change the way we treat human diseases.

Prothya Biosolutions processes around 3 million liters of plasma each year for several international partners.

This change in focus entailed a change in corporate culture. Prothya has a clear vision we call DRIVE, embodying the core values on which our organization is founded.

Do you want to play an active role in improving the health of millions of patients? Would you like to be our partner or future colleague at the forefront of new developments in the Protein Therapy Development, Processing and Manufacturing?

Then you are welcome at Prothya Biosolutions!

Listed Jobs

Company Name

Prothya Biosolutions

Job Title

Data Science Specialist

Job Description

Job title: Data Science Specialist Role Summary: Integrate GMP-regulated manufacturing data with advanced analytics to support quality reviews, compliance reporting, and continuous improvement within pharmaceutical production. Expectations: Deliver accurate, statistically validated PQR/QRR reports; apply machine learning, NLP, and predictive modeling to identify trends and root causes; collaborate cross-functionally to enhance compliance and process quality. Key Responsibilities: - Prepare, review, and statistically evaluate Product Quality Reviews (PQR) and Quality Review Reports (QRR) in line with GMP standards. - Merge structured and unstructured datasets to uncover trends, deviations, and correlations. - Develop and implement statistical, ML, and NLP models for quality monitoring and deviation tracking. - Provide quantitative support for investigations, change controls, and CAPA initiatives. - Liaise with technical and non‑technical teams to drive data‑driven continuous improvement. Required Skills: - Proficiency in Python and SQL; experience in C++ and data analysis tools (Minitab, Tableau, Power BI). - Knowledge of ML/NLP frameworks such as scikit‑learn, TensorFlow, spaCy, and LLM-based tools. - Strong statistical analysis and data visualization capabilities. - Excellent written and verbal communication in English; additional language skills advantageous. Required Education & Certifications: - MSc in Pharmaceutical Science, Data Science, Engineering, Mathematics, Chemistry, Computer Science, or related field. - Minimum of 2 years experience in a GMP‑regulated manufacturing or quality analytics environment. - Demonstrated expertise in PQR/APR/QRR reporting and compliance documentation.

Neder-over-heembeek, Belgium

On site

17-11-2025