Job description

  • Generates or oversees the generation of data or other information under GLP and GMP conditions and prepares and reviews appropriate reports for the transfer of information to clients.
  • Operates, maintains, and calibrates all job-relavent instrumentation and equipment as necessary.
  • Responsible for accurately recording data and observations, calculations, and reporting of data.
  • Ensures proper documentation of all activities involving samples, standards, controlled substances, and stability samples associate with projects as dictated by GLPs and cGMPS.
  • Provides basic training on instrumentation and equipment to less experienced personnel.
  • Notifies Supervisor of sample management issues, problems, corrective actions, potential efficiency improvements, etc.
  • Manages progress on assigned projects sot aht they meet the stated objective in the stated time-line.
  • Other duties as assigned.

Desired Skills and Experience

Bachelor or Master’s of Science required

7-12 years laboratory experience required

5+ years pharma experience

Analytical Method Development/Method Validation experience required

Able to multi-task and produce quality results.

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