3 - 5 years

0 Lacs

Posted:2 weeks ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Role & responsibilities

MD / MV and Study handling

  • Perform method development and method validation using ligand binding assays, cell-based assays and LC-MS/MS based assays.
  • Perform study sample analysis for the respective projects as delegated by the supervisor.
  • Document and compile raw data, unforeseen event, file note and deviation.
  • Interpret the data / result and perform troubleshooting if required.
  • Complete MD/MV and Study efficiently as per the defined timelines.

Inventory management

  • Responsible for timely procurement of chemicals/reagents/consumables and maintaining inventory for MD/MV and study sample analysis related activities.

Preparation of documents

  • Responsible for preparation of SOPs, Protocols, Plans/STPs/Reports/Lab manuals as and when required.

QC/QA related

  • Respond to relevant QC and QA queries in co-ordination with supervisor and QC respectively.

Equipment / Software related

  • Ensure timely Calibration / Maintenance / PM of equipment in co-ordination with vendor/service engineer.
  • Perform calibration and performance check for balances and pH meter on daily basis.

Archival

  • Assist in archival related activity as and when required.

Training

  • Get trained in SOPs, GCLP and other applicable guidelines as per the requirement.
  • Train junior team members as and when required.
  • Follow general Biosafety procedures, Emergency procedures and Organizational Policies /Values.

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Veeda CR logo
Veeda CR

Clinical Research, Biotechnology

Los Angeles

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