This is a temporary contractor opportunity at Novartis
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!
Novartis partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit.
Ready to work with/through Magnit at Novartis? Please read on…
Job Purpose:
The global pharmaceutical intelligence & Forensics strategy is fully embedded in our Anti-falsified medicine program, which is destined to combat pharmaceutical crime and create the conditions to bring counterfeiters and illegal traders to justice, recover losses through legal action, improve patient safety, preserve the client’s reputation, and create a tangible return on investment for the business.
The Authentifield Validation scientist is a highly specialized and technical role, reporting functionally and operationally to the Anti-Falsified Medicines, Director PharmINT & Forensics in Anti-Falsified Medicines CoE in Global Security.
The primary responsibility of this role is to ensuring the accuracy and reliability of our chemometric models, reviewing field test results, supporting laboratory experiments, and conducting comprehensive data analysis using Jupyter Notebook. The Validation scientist will collaborate closely with PharmINT associates and other stakeholders to develop, build, or continuously review the requirements for both Authentifield and PharmINT. All duties must be performed in strict adherence to our high standards for technical excellence, environmental compliance, and health and safety regulations.
Major Activities & Accountabilities:
1. Validation of Chemometric Models: Conduct thorough validation tests on chemometric mod-els to ensure their accuracy and reliability. This includes designing validation protocols, exe-cuting tests, and analyzing results. Maintain detailed documentation of validation processes, including validation protocols, sample materials, and test results. Continuously improve vali-dation methodologies to enhance model performance and robustness.
2. Review of Field Test Results: Analyze and review results from field tests conducted with Au-thentifield sensors. Ensure that the results meet the required standards and provide insights for improvement. Collaborate with field teams to address any discrepancies or issues identi-fied during the review process. Prepare comprehensive reports summarizing field test find-ings and recommendations for further action.
3. Support of Laboratory Experiments: Collaborate with laboratory teams to support and exe-cute experiments related to the validation of chemometric models. This includes preparing experimental setups, conducting tests, and analyzing experimental data. Ensure timely and accurate completion of laboratory tasks and maintain meticulous records of experimental procedures and results. Provide technical support and guidance to laboratory personnel as needed.
4. Data Analysis: Develop and use Jupyter Notebook for data analysis. This involves writing and executing Python scripts to process and analyze large datasets, visualize data trends, and generate meaningful insights. Interpret and present data findings to support decision-making processes. Continuously explore and implement new data analysis techniques to enhance the quality and efficiency of data analysis workflows.
5. 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 requirement:
1. Strong analytical and problem-solving skills.
2. Proven experience in chemometric model validation and data analysis.
3. Proficiency in Python and experience with Jupyter Notebook.
4. Strong analytical and problem-solving skills.
5. Excellent communication and interpersonal skills.
6. Ability to work independently and as part of a team.
7. Detail-oriented with a strong commitment to accuracy and quality.
8. Excellent communication and interpersonal skills.
9. Experience with system integration and project management.
10. Knowledge of regulatory requirements related to pharmaceutical supply chains is a plus.
11. Familiarity with falsified medicines detection technologies and methodologies.
12. Understanding of data privacy and security standards.
13. 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 like you. Collaborating, supporting and inspiring each other. Combining 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 [email protected].
