Job Description
#
# Follow cGMP and GDP in day to day activities.
# Comply with data integrity and relevant company policies.
# Preparation, review and sign up of documents like log books, formats, annexure, label and other records.
...
...literature review, evaluation of individual cases or signal detection, and responds to safety related questions appropriately.
• Performs medical assessment and related activities for cases whenever required, incl...
This is a remote position.
What roles and responsibilities will be performed by the selected candidate?
1. Review and optimize the Dev Ops processes of CosmosDB databases across project
2. Review the CosmosDB data saving and retrieval pa...
About the Role
Job Purpose
In close collaboration with the Global Program Safety Lead (GPSL) provides robust safety evaluation expertise and medical innovation in order to improve patients’ lives and impact on overall Novartis results. As a mem...
About the role
Location : #L1 Hybrid
The role is part of Security Operations in Vulnerability Services team. The person will focus on reducing risk exposure from security vulnerabilities with major focus on solution design, architecture, and V...
Job Description
1.1 To ensure and adhere Organization Safety/Quality policies, Procedures and norms effective implementation from time to time.
1.2 Ensure the adherence of SHE standards and policies across the plant with respect to MSI
1.3...
About the Role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all di...
About the role
Your responsibilities include but not are limited to:
• Regulatory Strategy -Responsible for implementing regulatory strategy and managing operational activities for assigned regions.Provides input into global regulatory strategy...
Job Description
In this role you will be reviewing online search results in order to improve their content and quality. You will be required to provide feedback and analysis on content found in search engine results and provide ratings on the...
About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all d...
