Quality Control Technician - Valencia, CA (1st Shift)

Staffmark Group

California (MO)

On-site

USD 28,000 - 33,000

Full time

11 days ago

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Benefits offered by this job

Competitive weekly pay
Medical, dental and vision coverage
Life and disability insurance
Optional 401(k) plan
Quality-focused work environment

Job summary

Staffmark Group currently seeks a Quality Control Technician in Valencia, CA to ensure production runs smoothly by inspecting, testing, and approving finished parts. The role requires attention to detail and experience in GMP-regulated environments, with data-entry responsibilities and documentation control.

Ideal candidates will have a high school diploma or equivalent and at least one year in a GMP or laboratory setting.

Qualifications

  • High school diploma or equivalent required; associate degree in a scientific, laboratory, or administrative field preferred.

Responsibilities

  • Maintain accurate, organized quality control records, logs, and documentation in line with GDP and GMP standards.
  • Scan, file, and retrieve certificates of analysis, laboratory worksheets, environmental monitoring records, and equipment logs.
  • Support sample management, including labeling, tracking, and coordinating transfers for raw material, in-process, finished product, and retain samples.
  • Enter laboratory data into spreadsheets and electronic systems with strong attention to detail and accuracy.
  • Assist with document preparation for audits, inspections, and internal quality reviews.
  • Coordinate calibration and maintenance scheduling for laboratory equipment.
  • Communicate across QC, QA, warehouse, and production teams to support compliance and efficiency.

Skills

Data entry
Recordkeeping
Electronic documentation
Attention to detail

Education

High school diploma or equivalent
Associate degree preferred

Job description

Staffmark Group currently seeks a Quality Control Technician in Valencia, CA to ensure production runs smoothly by inspecting, testing, and approving finished parts. The role requires attention to detail and experience in GMP-regulated environments, with data-entry responsibilities and documentation control.

Ideal candidates will have a high school diploma or equivalent and at least one year in a GMP or laboratory setting.

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