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Document Control & Quality Compliance Specialist

Job in Torrance, Los Angeles County, California, 90504, USA
Listing for: Sincerus Solutions
Full Time position
Listed on 2026-08-25
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 55000 - 85000 USD Yearly USD 55000.00 85000.00 YEAR
Job Description & How to Apply Below

Job Description

Job Description

Job Summary

Perform Document Control and Quality Assurance activities related to document management and compliance audit activities. This is a hands‑on onsite role supporting quality systems, controlled documentation, engineering change processes, and RMA activities.

Key Responsibilities
  • Coordinate document control activities including distribution, auditing, tracking, and reporting of controlled documents.
  • Manage archival activities for controlled documents and validation files.
  • Implement and administer the electronic document management system.
  • Manage the ECR/ECO process and facilitate weekly review meetings.
  • Support Quality Management System audits and compliance activities.
  • Review specification changes from customers and agencies.
  • Coordinate RMA activities and maintain reporting metrics.
Education & Experience
  • High School Diploma or equivalent.
  • Bachelor’s degree in a technical field preferred.
  • 1-3 years of manufacturing experience.
  • Experience with engineering/manufacturing documentation and documentation practices.
  • Knowledge of ISO 13485, ISO 9001, FDA 21 CFR Part 820, and AS9100 is a plus.
Must-Have Requirements
  • High School Diploma or equivalent.
  • 1-3 years of experience in a manufacturing environment.
  • Experience working with engineering and manufacturing documentation.
  • Knowledge of document control procedures and good documentation practices.
  • Strong Microsoft Excel and Microsoft Office proficiency.
  • Excellent organizational skills and attention to detail.
  • Ability to manage multiple priorities and work independently.
  • Strong written and verbal communication skills.
  • Preferred Qualifications
    • Bachelor's Degree in a technical field.
    • Experience with electronic document management systems (EDMS).
    • Knowledge of ISO 13485, ISO 9001, FDA 21 CFR Part 820, and/or AS9100 standards.
    • Experience managing Engineering Change Requests (ECRs) and Engineering Change Orders (ECOs).
    • Experience supporting quality audits and compliance activities.
    • Background in electronics, aerospace, medical device, or other regulated manufacturing environments.
    • Veterans are encouraged to apply.
    Skills & Abilities
    • Strong attention to detail and organizational skills.
    • Ability to manage multiple priorities in a fast-paced environment.
    • Strong communication and collaboration skills.
    • Microsoft Excel and Office proficiency.
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