QC Support Analyst I

SGS Consulting

Sacramento (CA)

On-site

USD 42,000 - 64,000

Full time

5 days ago
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Job summary

SGS Consulting is seeking a Laboratory Analyst to perform routine GMP/GLP testing and analyze data against specifications. You will manage QC inventories and maintain lab cleanliness, equipment calibration, and documentation.

The role requires a science bachelor’s degree and familiarity with ERP/LIMS systems; strong regulatory knowledge is preferred. On-site position with standard lab hours.

Qualifications

  • Bachelor’s degree in a science-related field.

Responsibilities

  • Performs routine testing using GMP/GLP practices.
  • Analyzes data and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
  • Maintains product and QC material inventories.
  • Maintains the laboratory and stocks testing materials.
  • Maintains and calibrates equipment or submits items for calibration as needed.
  • Completes training in a timely manner and maintains records.
  • Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
  • Prepares documents for storage in the document management system and manages original data files.

Skills

Industrial lab exp
Computer skills
GMP/GLP knowledge
ERP/LIMS/QS

Education

Bachelor’s degree in science

Job description

Job Responsibilities:
  • Performs routine testing using GMP/GLP practices.
  • Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
  • Responsible for maintaining product and QC material inventories.
  • Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
  • Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
  • Responsible for completing training in a timely manner and maintaining the records.
  • Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
  • Prepares documents for storage in our document management system and manages original data files.
Skills:
  • 1 to 2 years of industrial lab experience (preferably QC)
  • Intermediate computer skills (i.e., Microsoft programs)
  • Working knowledge of industry/regulatory standards and GMP/GLP requirements
  • Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QS
Education/Experience:
  • Bachelor’s degree in a science-related field
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