Veeda Lifesciences is organizing a Walk-In Drive for multiple positions on Sunday,1st February 2025.
Role & responsibilities – BQM(QC):
- Perform Quality review of bioanalytical data, including chromatograms, calibration curves, QC samples, and final reports.
- Review bioanalytical method validation (BMV), partial validation, and cross-validation reports for compliance with regulatory guidelines.
- Ensure adherence to GLP, GCP, US FDA, EMA, and CDSCO requirements.
- Verify data integrity (ALCOA+) and ensure traceability of raw data.
- Review study plans, protocols, SOPs, and amendments.
Role & responsibilities – Custodian:
- Receive, label, log, store, and retrieve biological samples (plasma, serum, urine, tissue, etc.) as per SOPs.
- Receive, label, log, store, retrieve working and reference standards and Analytical Columns as per SOPs.
- Maintain sample storage areas such as deep freezers, refrigerators, and cold rooms under defined conditions.
- Monitor and record storage temperatures; report deviations immediately.
- Ensure proper segregation, handling, and disposal of biohazard and chemical waste.
- Maintain accurate inventory records, sample chain-of-custody logs, and tracking documentation.
Role & responsibilities – Instrumentation Engineer:
- Assist in routine inspections, calibration, and preventive maintenance of laboratory instruments and equipment.
- Support troubleshooting activities and ensure timely repairs to minimize equipment downtime.
- Maintain accurate documentation of maintenance activities, equipment history, and service schedules.
- Ensure compliance with laboratory safety protocols, quality standards, and regulatory requirements.
- Coordinate with external vendors and service partners for specialized maintenance, calibration, and technical support.
Role & responsibilities – Lab Automation:
- To manage the sample manager LIMS for the overall Bioanalytical lab execution processes.
- Configurations of the lab execution method parameters in sample manager
- LIMS and other such software in coordination with vendor as per requirements.
- Preparation and configurations of the new methods for lab execution system based on method specific requirement.
- To update and configure the existing methods for lab execution system based on method specific requirement / based on revised SOPs.
- SOPs linked with automated processes.
- Execution for process implementation/ simplification /digitalization.
- To oversee and manage the implemented system / Software for effective and smooth operations.
- System evaluation of different vendors and conclude fit for business requirement.
- Document preparation for CSV Activities.
Role & responsibilities – LIMS Operator:
- Creation of Project, Study (Method Validation/Project Sample Analysis) and Master Assay based on Method SoP.
- To develop Study Design in the application based on protocol, Sample Handling and Tracking procedure as per sample shipment within system Based on request (from analyst) Analytical Run (work-list and run sequence) creation.
- Result import and perform Regression within system/application, Raw results generation (of Method Validation, Study Sample analysis, Reassay identification and Reassay report generation).
- To submit all reports to analysts and GL for their review.
- To generate final summary report tables (MV Reports and Study Reports) for compilation by report writers and sample concentration data (to Statistical department) for Pk Analysis.
- To generate Barcode labels through Watson LIMS for clinical phase study.
Role & responsibilities – Document Controller:
- Request to QAD for the requirement of controlled form, Log format, method book, SOP or other controlled documents.
- Maintain the copy of controlled form, SOP or other controlled documents.
- Issuance of controlled form to respective team for validation and project sample analysis as and when required.
- Maintaining the accountability of forms, format, log formats and method books.
- Maintain the copy of standard operating procedures within department.
- To return the obsolete / previous version SOPs to QAD when revised.
- To get the amended or extended SOPs stamped by QAD.
- Reconciliation and Archiving of raw data generated during MD, MV and PSA.
- Reconciliation and Archiving of calibration and maintenance data of equipments.
- Reconciliation and Archiving of log format, PTR, system related data and others.
- Archiving of all the respective data related to bioanalytical department
Walk-In Interview Details:
- Date: 1st February, 2026
- Time: 10.00 AM – 3.00 PM
- Venue: Satyamev Corporate, Corporate Rd, near Shalin Bungalows, Opp. Prahalad Nagar Fire Station , Prahalad Nagar, Ahmedabad, Gujarat 380015.
Required Documents: Interested and eligible candidates can kindly bring your:
- Updated resume,
- Passport size photo,
- Educational documents
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