Experience Required: 12 to 15 Years

Location:
Peenya, Bangalore Job Responsibilities MD / MV and Study handling:
• Acts as an Analytical Project Manager for GCLP studies as delegated by TFM/Deputy TFM.
• Ensure and guide the team for method development and method validation using ligand binding assays, cell-based assays and LC-MS/MS based assays and study related activities.
• Review of raw data, unforeseen events, file notes and deviation.
• Strategize and plan MD/MV and study sample analysis efficiently and deliver the projects within the defined timelines. Inventory management
• Ensure timely procurement of chemicals/reagents/consumables and maintaining inventory for MD/MV and study sample analysis related activities. Preparation / Review of documents




• Responsible for preparation/review of current Policies, SOPs, Protocols, Plans/STPs/Reports/Lab manuals and their implementation. QC/QA and regulatory related
• Reply to relevant QC and QA queries in co-ordination with team members and QC respectively.
• Responsible for study audit from sponsor.
• Responsible for the compliance to relevant audit & regulatory/sponsor findings. Equipment / Software related
• Review of IQ/OQ/PQ, calibration and maintenance documents of equipment/software.
• Ensure timely Calibration/ Maintenance / PM of equipment.
• Review of Audit trails based on the requirement.

📌 Group Lead (Bengaluru)
🏢 Veeda Lifesciences
📍 Bengaluru