JVT Advisors

Quality Control Analyst 1

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Location: Bedford, Massachusetts 01730
Employment Type: Contract

Job Description

Contract Length:  6 months

Job Summary:  The Quality Control Analyst is primarily responsible for the activities and procedures which are required to sample and test raw materials, work-in-process samples, finished goods, and stability samples under cGMP conditions.

Responsibilities: 

  • Testing of incoming raw material according to USP, EP, or ACS Reagent Index
  • Testing of in process and release manufacturing samples, stability samples and Engineering/R&D samples using the following instrumentation/techniques:

UV/Vis Spectrophotometry

FTIR Spectrophotometry

Auto & Manual Titrations

Freezing Point & Vapor Pressure Osmometry

Absolute Viscosity using Brookfield Cone/Plate Viscometer

Intrinsic Viscosity using Ubbelohde Tube and Dilute Solution Viscometer

pH Meter

TOC Analyzer

Conductivity Meter

  • Complete required documentation for all work activities according to Good Documentation Practices

Requirements:

 

  • 0-2 years testing experience in FDA regulated pharmaceuticals or medical device industries; internship experience considered
  • Demonstrated experience with basic lab instrumentation including UV/vis and FTIR spectrophotometers, pH Meters, and Osmometers
  • Demonstrated experience with basic lab instrumentation including UV/vis and FTIR spectrophotometers, pH Meters, and Osmometers

 

Trevor Hoffman

Technical Recruiter

Trevor recruits for JVT's Life Sciences and Technology Practices where he specializes in finding, screening, and placing top-tier industry innovators at companies across multiple markets and verticals.

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