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  • Quality Control at AllSTEM East Greenbush, New York

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  • East Greenbush, New York 12061 United States View Map

Summary

Quality Control Analyst

Duration: 6+ Months

Location: Rensselaer, NY 12144

Qualifications:

  • Bachelor's with major in Chemistry or related scientific discipline with a minimum of 6 years of experience in a QC laboratory environment OR equivalent combination of relevant education and experience may be substituted as appropriate
  • Investigations experience including root cause analysis, writing, and CAPA identification

Monday - Friday 8am-5pm

Responsibilities:

  • Work with QC and cross functional team as needed to meet required QC investigation deadlines in a proficient manner, while driving to root cause, and identifying the appropriate & effective corrective and preventive action.
  • Ensure QC investigations are initiated in a timely manner, initial impact completed and submitted for QA reviews within stipulated timeframes
  • Conduct and document investigations as needed, while also working with customers as required.
  • Conduct, and document OOS investigations, including coordination with customers as required by quality agreements and regulatory commitments.
  • Apply 6M, 5 Why or fishbone analysis to drive root cause
  • All investigations will follow procedures in accordance with cGMP's.
  • Work with the team to document and drive critical investigations to closure.
  • Maintain metrics for the laboratories to identify CAPA opportunities including, analyst error rate, equipment failure rate, and test method issues.
  • Ensure all investigations are executed in full compliance with cGMPs, Curia SOPs, and global quality standards.
  • Work with the team to develop investigation strategies to meet customer commitments and requirements.
  • Provide investigation updates to cross functional areas and management, as required.
  • Develop an expertise in documenting investigations and create templates to use for ease of reference and consistency.
  • Identify CAPA's and update training modules to reduce analyst error rate
  • Work independently and with the QC team as the primary investigator on all critical laboratory related investigations.

Job Description

Quality Control Analyst

Duration: 6+ Months

Location: Rensselaer, NY 12144

Qualifications:

  • Bachelor's with major in Chemistry or related scientific discipline with a minimum of 6 years of experience in a QC laboratory environment OR equivalent combination of relevant education and experience may be substituted as appropriate
  • Investigations experience including root cause analysis, writing, and CAPA identification

Monday - Friday 8am-5pm

Responsibilities:

  • Work with QC and cross functional team as needed to meet required QC investigation deadlines in a proficient manner, while driving to root cause, and identifying the appropriate & effective corrective and preventive action.
  • Ensure QC investigations are initiated in a timely manner, initial impact completed and submitted for QA reviews within stipulated timeframes
  • Conduct and document investigations as needed, while also working with customers as required.
  • Conduct, and document OOS investigations, including coordination with customers as required by quality agreements and regulatory commitments.
  • Apply 6M, 5 Why or fishbone analysis to drive root cause
  • All investigations will follow procedures in accordance with cGMP's.
  • Work with the team to document and drive critical investigations to closure.
  • Maintain metrics for the laboratories to identify CAPA opportunities including, analyst error rate, equipment failure rate, and test method issues.
  • Ensure all investigations are executed in full compliance with cGMPs, Curia SOPs, and global quality standards.
  • Work with the team to develop investigation strategies to meet customer commitments and requirements.
  • Provide investigation updates to cross functional areas and management, as required.
  • Develop an expertise in documenting investigations and create templates to use for ease of reference and consistency.
  • Identify CAPA's and update training modules to reduce analyst error rate
  • Work independently and with the QC team as the primary investigator on all critical laboratory related investigations.
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