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QA Specialist II- Torrance, CA.

Job in Torrance, Los Angeles County, California, 90501, USA
Listing for: Prime Matter Labs
Full Time position
Listed on 2026-07-01
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below

QA Specialist II

The QA Specialist II supports and drives the quality assurance activities for the manufacturing of cosmetic and OTC drug products. This role ensures compliance with FDA regulations, customer requirements, and internal quality standards. The ideal candidate will be detail-oriented, organized, and eager to grow within a fast-paced, regulated manufacturing environment. Essential duties and responsibilities include completing all tasks and assignments in a safe and timely manner, striving toward continuous self improvement in personal productivity, reviewing and approving batch records, specifications, and quality documentation, conducting in-process checks and supporting final product release, leading and assisting in investigations of deviations, non-conformances, and customer complaints, driving reviews and tracking of quality systems documentation such as training, change controls, CAPA, audit commitments, supporting internal audits and regulatory inspection readiness, assisting and leading efforts to ensure compliance with GMP, FDA regulations (21 CFR Parts 210/211), and ISO 22716 for cosmetics and OTC drug products, helping maintain and update SOPs and quality documentation, collaborating with cross-functional teams to support continuous improvement initiatives, maintaining accurate and organized quality records, and aiding in collection, analysis and trending of QC data and Quality metrics.

Preferred skills include exposure to 21 CFR Parts 210/211 and ISO 22716, experience in a contract manufacturing setting, familiarity with OTC monograph compliance and labeling, and willingness to learn and grow within a regulated industry.

Qualifications include a minimum of 3 years of experience in a QA or regulated manufacturing environment preferred (cosmetics or OTC drugs a plus), a bachelor's degree in a scientific or technical field (e.g., Chemistry, Biology, Pharmaceutical Sciences), working knowledge and understanding of GMP, FDA regulations, and quality systems, strong attention to detail and organizational skills, effective written and verbal communication skills, proficiency in Microsoft Office and familiarity with electronic quality systems is a plus, and maintaining an exemplary attendance and punctuality performance record.

At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer.

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