Website:
veedalifesciences.com
Job details:
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 new 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.
Click on Apply to know more.
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