Job ID: 1796903
Reference Code: TESS -Bilingual-Spanish Quality Analyst
Job Summary
A growing manufacturing organization in Gardena, CA is seeking a Bilingual Spanish Quality Analyst to support quality assurance, compliance, and continuous improvement within a regulated production environment. This direct hire opportunity is ideal for a quality professional with experience in personal care, OTC, or related manufacturing who is skilled in investigations, root cause analysis, CAPA, audits, and quality documentation.
The Bilingual Spanish Quality Analyst will play a key role in maintaining cGMP compliance, supporting production teams, resolving quality issues, and helping strengthen quality systems across manufacturing, compounding, and production operations. This is a strong opportunity to join a collaborative environment with supportive leadership, positive teamwork, and the ability to make a meaningful impact on product quality, process improvement, and operational excellence.
Key Responsibilities
- Maintain quality documentation, records, SOPs, protocols, technical reports, and related files in accordance with GMP and GDP requirements.
- Conduct quality investigations, root cause analysis, non-conformance reviews, customer complaint investigations, and OOS event management.
- Develop, implement, and monitor corrective and preventive actions to address quality issues and prevent recurrence.
- Perform internal audits across manufacturing, compounding, and production areas to ensure compliance with cGMP, regulatory standards, and internal procedures.
- Monitor manufacturing processes, identify quality trends, recommend improvements, and support continuous improvement initiatives.
- Collaborate with cross-functional teams and provide training on quality standards, procedures, documentation practices, and best practices.
Compensation and Benefits
- Salary range: $80,000 to $90,000 per year.
- Job type: Direct hire.
- Location: Gardena, CA.
Equal Opportunity Employer / Disabled / Protected Veterans
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For temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.
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https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Required Qualifications and Skills
- Conduct quality investigations, root cause analysis, CAPA, NCR, OOS, and customer complaint resolution.
- Support cGMP compliance, internal audits, SOP management, and Good Documentation Practices.
- Monitor production and manufacturing processes to ensure quality standards are consistently met.
- Partner with manufacturing, compounding, production, and other teams to resolve quality issues and improve processes.
- Bachelor’s degree in Manufacturing, Chemistry, Biology, Engineering, or a related field.
- Bilingual in English and Spanish is required.
- Quality Assurance experience in a manufacturing environment, with experience level aligned to 6-10 years preferred for this role.
- Minimum of 2 years of hands-on quality assurance experience in manufacturing.
- Strong understanding of quality systems, cGMP regulations, GDP, industry standards, and regulatory compliance expectations.
- Experience conducting quality inspections, audits, investigations, testing, and documentation reviews.
- Proficiency with QA databases, Microsoft Office Suite, and quality management systems.
- Strong analytical, organizational, communication, and problem-solving skills.
- Ability to work effectively with cross-functional teams in a fast-paced manufacturing environment.
Preferred Qualifications
- Experience in OTC, personal care, cosmetics, pharmaceutical, or similarly regulated manufacturing environments.
- Experience developing and revising SOPs, protocols, technical reports, and quality documentation.
- Background supporting continuous improvement, process optimization, and quality system enhancements.
- Strong ability to train employees on quality procedures, GMP expectations, and documentation best practices.