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Job Purpose
The global pharmaceutical intelligence & forensic strategy is fully embedded in our Anti‑falsified medicine program. The role combats pharmaceutical crime, protects patient safety, preserves the client’s reputation, and delivers a tangible return on investment. The Authentifield Validation Scientist reports to the Anti‑Falsified Medicines Director and works within the Anti‑Falsified Medicines CoE in Global Security.
Major Activities & Accountabilities
* Validation of Chemometric Models: Conduct thorough validation tests, design protocols, execute tests, analyze results, and maintain detailed documentation.
* Review of Field Test Results: Analyze field‑test outcomes, ensure compliance with standards, collaborate with field teams, and prepare comprehensive reports.
* Support of Laboratory Experiments: Collaborate with lab teams to execute experiments, maintain records, and provide technical guidance.
* Data Analysis: Develop and use Jupyter Notebook for data analysis, write Python scripts, visualize trends, and present insights.
* Stakeholder Communication: Communicate findings and recommendations to stakeholders, including senior management.
Ideal Background
Education (minimum/desirable): Bachelor's or Master's degree in Analytical Chemistry, Data Science, or a related field. A master’s degree is a plus.
Languages: Fluent in English.
Experience / Professional Requirements
* Strong analytical and problem‑solving skills.
* Proven experience in chemometric model validation and data analysis.
* Proficiency in Python and experience with Jupyter Notebook.
* Excellent communication and interpersonal skills.
* Ability to work independently and as part of a team.
* Detail‑oriented with a strong commitment to accuracy and quality.
* Experience with system integration and project management.
* Knowledge of regulatory requirements related to pharmaceutical supply chains is a plus.
* Familiarity with falsified medicines detection technologies and methodologies.
* Understanding of data privacy and security standards.
* Strong documentation skills, including creating detailed business requirement documents (BRDs) and functional specifications.
Workload
100% (40 hours per week)
Role Type
Onsite
Required Start Date
January 2026
Contract
2 years
Why Novartis
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people who collaborate, support, and inspire each other to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
EEO Statement
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accommodation
If you require reasonable accommodation in completing this application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.
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