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Method Qualification Development/Test Analyst

In Massachusetts / United States

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Method Qualification Development/Test Analyst   

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JOB TITLE:

Method Qualification Development/Test Analyst

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Lexington Massachusetts / United States

JOB DESCRIPTION:

Responsibilities:

  • Perform QC test methods and review results for qPCR, WES Protein Simple, ELISA, Dynamic Light Scattering, and Nanoparticle Tracking Analysis.
  • Daily, hands-on work in the laboratory
  • Write and develops method validation protocols, reports, and test methods.
  • Review of release, stability, and characterization data, including technical review of change control documentation and reports, deviations, and OOS.

Requirement:

  • BS and/or MS degree in biochemistry, cell biology, and/or molecular biology discipline.
  • At least 2 years work experience in a GMP environment
  • Previous experience Developing and testing for qPCR, WES Protein Simple, ELISA, Dynamic Light Scattering, and Nanoparticle Tracking Analysis
  • Proven experience writing and developing method validation protocols, reports, and test methods.
  • Review of release, stability, and characterization data, including technical review of change control documentation and reports, deviations, and OOS;
  • Technology environment the consultant will be working in Kingfisher Flex huge plus
  • qPCR experience working with Kingfisher Flex Instrument is preferred

Position Details

POSTED:

Jul 05, 2021

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S16204865143003765

LOCATION:

Massachusetts / United States

CITY:

Lexington

Job Origin:

CEIPAL_ORGANIC_FEED

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In Dallas Fort Worth
Aug 19, 2017 9am-6pm
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Method Qualification Development/Test Analyst    Apply

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Responsibilities:

  • Perform QC test methods and review results for qPCR, WES Protein Simple, ELISA, Dynamic Light Scattering, and Nanoparticle Tracking Analysis.
  • Daily, hands-on work in the laboratory
  • Write and develops method validation protocols, reports, and test methods.
  • Review of release, stability, and characterization data, including technical review of change control documentation and reports, deviations, and OOS.

Requirement:

  • BS and/or MS degree in biochemistry, cell biology, and/or molecular biology discipline.
  • At least 2 years work experience in a GMP environment
  • Previous experience Developing and testing for qPCR, WES Protein Simple, ELISA, Dynamic Light Scattering, and Nanoparticle Tracking Analysis
  • Proven experience writing and developing method validation protocols, reports, and test methods.
  • Review of release, stability, and characterization data, including technical review of change control documentation and reports, deviations, and OOS;
  • Technology environment the consultant will be working in Kingfisher Flex huge plus
  • qPCR experience working with Kingfisher Flex Instrument is preferred


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