Quality Assurance Inspector I

Argen Corp

San Diego, CA

JOB DETAILS
SKILLS
Administrative Procedures, Code of Federal Regulations, Communication Skills, Compensation and Benefits, Computer Systems, Current Good Manufacturing Practice (cGMP), Dentistry, Detail Oriented, FDA Requirements, GMP (Good Manufacturing Practices), HRIS/HRMS, High School Diploma, Housekeeping/Cleaning, ISO (International Organization for Standardization), Internal Audit, Maintain Compliance, Manufacturing, Onboarding, Organizational Skills, Presentation/Verbal Skills, Problem Solving Skills, Product Positioning, Project/Program Management, Quality Assurance, Quality Control, Quality Metrics, Regulations, Regulatory Compliance, Safety Standards, Safety/Work Safety, Team Player, Technical Drawing, Technical Writing, Testing, Time Management, Traceability, Writing Skills
LOCATION
San Diego, CA
POSTED
16 days ago

Join Argen as a Quality Assurance Inspector I

Location: 8515 Miralani Dr, San Diego, CA 92126

Schedule: Monday-Friday, 8:00am - 4:30pm

Argen, a global leader in digital dentistry and dental materials, is seeking an HR Generalist to support benefits & LOA administration, HRIS reporting, recruiting, onboarding, and compliance. If you thrive on details, communication, and project management, this role is for you.

About the Role

The Quality Assurance Inspector I plays a pivotal role in ensuring the quality and integrity of Argen products. This position is responsible for inspecting in-process and finished goods within manufacturing areas to ensure compliance with ISO 13485:2016, FDA regulations, customer specifications, Argen requirements, and applicable procedures.

Key Responsibilities

  • Conduct in-process and final inspections and testing as required.
  • Perform visual inspections of finished products.
  • Participate in internal assessments and audits.
  • Maintain accurate inspection and test records.
  • Identify and properly label non-conforming materials.
  • Communicate product/material acceptability to production personnel.
  • Assist with technical problem-solving and special projects.
  • Maintain lot traceability, log sheets, and housekeeping standards.
  • Follow safety policies and regulations to ensure safe work practices.
  • Ensure lab cleanliness and safety standards are upheld.
  • Perform thorough inspections during and after production to ensure quality and compliance.
  • Verify product labeling for accuracy and regulatory compliance.
  • Clear and prepare production lines for subsequent runs.
  • Review and validate Device History Records (DHRs) for completeness and compliance.
  • Perform other duties as assigned.

What You Bring

  • High school diploma or equivalent required.
  • Experience in a GMP-regulated facility is a plus.
  • Completion of 8 hours of Quality Training (PTC) required.
  • Strong attention to detail.
  • Proficiency in basic arithmetic and problem-solving.
  • Understanding of raw materials, production processes, and quality control.
  • Familiarity with administrative procedures and computer systems.
  • Effective written and verbal communication skills.
  • Ability to interpret technical drawings, artwork, and procedures.
  • Commitment to safety and quality standards.
  • Ability to follow site protocols, policies, and procedures.
  • Flexible, motivated, and capable of working independently.
  • Strong organizational and time-management skills.
  • Problem-solving abilities.
  • Ability to learn technical concepts through documentation and training.
  • Preferred knowledge of regulatory standards including: cGMP, ISO 13485, 21 CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16/2013, MHLW MO 169, TG(MD)R Sch3

Why You'll Love Working at Argen

  • Competitive pay and full benefits package
  • Medical, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and wellness programs
  • Employee events and exclusive discounts
  • A collaborative, innovative, growth-focused culture

About the Company

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Argen Corp