Quality Control Analyst II

    • Nitto Denko Corp.
  • Milford, MA
  • Posted 49 days ago | Updated 6 hours ago

Overview

On Site
Compensation information provided in the description
Full Time

Skills

Authorization
Good Manufacturing Practice
Regulatory Compliance
Documentation
SOP
Testing
Training
Chemistry
Biology
Quality Control
GMP
Analytical Skill
Test Equipment
HPLC
UV
LCMS

Job Details

Job Description

About this opportunity :

The QC Analyst II is responsible for conducting routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required.

Key Responsibilities:

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  • Conduct a wide variety of routine testing.
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  • Test and analyze samples in a timely manner in support of project plans in accordance with cGMP guidelines.
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  • Review data for compliance against specifications and GMP regulations.
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  • Generate stability reports, and assist in the development of experimental procedures and protocols
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  • Assist with developing/revising documentation such as SOP, testing procedures and material specifications.
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  • Provide training and guidance to other analysts.
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Required Skills/Abilities:

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  • BS in chemistry, biology, or related discipline
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  • 2-5 years' experience as a QC analyst/chemist in a GMP environment
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  • Experience and familiarity with analytical testing equipment and methodology including HPLC, Karl Fischer, Spectrophotometry (UV/VIS), and LCMS
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The annualized salary range for this position is $65,900.00 - $86,300.00.
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