Bilingual QA/QC Coordinator — GMP Compliance (Orange)

Staffmark Group

California

On-site

USD 34,000 - 49,000

Full time

4 days ago
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Benefits offered by this job

Competitive weekly pay
Comprehensive benefits
Life Insurance and Disability
Optional 401(k) Plan
Quality-Focused Work Environment

Job summary

Staffmark Group is seeking a Bilingual Quality Coordinator in Orange, CA to inspect products, verify quality standards, and ensure final products meet customer expectations before shipping. The role emphasizes GMP compliance, meticulous record-keeping, and collaboration with cross-functional teams.

The position offers a Monday–Friday schedule (8-hour shift) with a pay rate of $30.00 per hour. Candidates should have QA/QC experience in GMP environments and strong attention to detail.

Qualifications

  • Minimum QA/QC experience in GMP-regulated manufacturing.
  • width:140;
  • Strong understanding of GMP requirements and quality systems.
  • Nice to have: experience with audits and CAPA.

Responsibilities

  • Review batch records and manufacturing documentation for accuracy and compliance.
  • Maintain QA/QC documentation.
  • Support internal and external audits.
  • Assist with investigations, deviations, and CAPA activities.
  • Monitor and support quality processes within manufacturing and packaging operations.
  • Ensure GMP compliance and company procedures.
  • File and organize quality records and reports.
  • Collaborate with cross-functional teams to support quality initiatives.
  • Assist with administrative and documentation-related quality activities.

Skills

QA/QC experience
GMP knowledge
Documentation
Attention to detail
Multitasking
Communication
Microsoft Office

Education

Bachelor's degree in a related field

Tools

Document management systems
Microsoft Office

Job description

Staffmark Group is seeking a Bilingual Quality Coordinator in Orange, CA to inspect products, verify quality standards, and ensure final products meet customer expectations before shipping. The role emphasizes GMP compliance, meticulous record-keeping, and collaboration with cross-functional teams.

The position offers a Monday–Friday schedule (8-hour shift) with a pay rate of $30.00 per hour. Candidates should have QA/QC experience in GMP environments and strong attention to detail.

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