Expert Science & Technology- Specialty Team (G

Design, plan and perform scientific experiments for projects at different clinical phases of drug substance and drug product with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports. Adhere to Quality metrics, Compliance and Good Documentation Practices following ALCOA+ principles, GLP, OQM, HSE, ISEC and Novartis guidelines. Should be a Team player by adding value in collaborating with other teams to support project deliverables within agreed timelines, mentoring new joiners, active participation in project meetings / networks / meetings and contributing to Team goals while meeting individual objectives. Responsible for Qualification of instruments / equipment’s (URS to Report) and periodic calibrations as per applicable site procedures. Ability to perform investigations, guide team members, communicate proactively and clearly to global stakeholders.