Bilingual QA/QC Specialist - GMP Compliance

Staffmark Group; Orange (CA); On-site; USD 62,000 - 78,000; Full time

Benefits offered by this job

Weekly pay

Benefits package

Insurance (life/disability)

401(k) plan

Quality-focused environment

Job summary

Staffmark Group in Orange, CA is hiring a Bilingual Quality Coordinator to inspect products and verify quality standards. The role focuses on ensuring every finished product meets customer expectations before leaving the facility.

Responsibilities include reviewing batch records, maintaining QA/QC documentation, supporting audits, and CAPA activities. The position requires GMP experience, strong attention to detail, and effective communication within a fast-paced manufacturing environment.

Qualifications

• QA/QC experience in a GMP-regulated manufacturing environment is required.
• Strong understanding of GMP requirements and quality systems.
• Excellent documentation and record-keeping skills.
• Strong attention to detail and organizational abilities.
• Ability to manage multiple priorities in a fast-paced environment.
• Effective communication and teamwork skills.

Responsibilities

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

Skills

QA/QC

GMP knowledge

Documentation

Detail oriented

Multi-tasking

Communication

MS Office

Education

Bachelor's degree preferred

Tools

Microsoft Office

Job description

Staffmark Group in Orange, CA is hiring a Bilingual Quality Coordinator to inspect products and verify quality standards. The role focuses on ensuring every finished product meets customer expectations before leaving the facility.

Responsibilities include reviewing batch records, maintaining QA/QC documentation, supporting audits, and CAPA activities. The position requires GMP experience, strong attention to detail, and effective communication within a fast-paced manufacturing environment.