Are you ready to bridge GMP compliance with advanced analytics?

Prothya Biosolutions is looking for a Data Science & Compliance Reporting Specialist to join our Product Support Team within the Operations Support Department. This hybrid role combines pharmaceutical manufacturing expertise with cutting-edge data science, machine learning, and digital transformation.

What you’ll do

• Lead the preparation, review, and statistical evaluation of Product Quality Reviews (PQR) and Quality Review Reports (QRR) in compliance with GMP standards.
• Integrate structured and unstructured data to uncover trends, deviations, and correlations.
• Apply statistics, ML, and NLP models to enhance quality monitoring and deviation tracking.
• Support investigations, change controls, and CAPA processes through quantitative root cause analysis and predictive modeling.
• Collaborate across technical and non-technical teams to drive continuous improvement.

What we’re looking for

• MSc in Pharmaceutical Science, Data Science, Engineering, Mathematics, Chemistry, Computer Science, or related field.
• 2+ years in a GMP-regulated manufacturing or quality analytics environment.
• Strong experience in PQR/APR/QRR reporting and compliance documentation.
• Proficiency in Python, SQL, C++, and tools like Minitab, Tableau, Power BI.
• Knowledge of ML/NLP frameworks (scikit-learn, TensorFlow, spaCy, LLM-based tools).
• Fluent in English; additional languages are a plus.

Why join us?

At Prothya Biosolutions, you’ll be part of a team that values innovation, collaboration, and continuous learning. This is your chance to make an impact in a dynamic environment where data meets compliance.

👉 Apply now and help us shape the future of pharmaceutical manufacturing!