QC Inspector I

Hygiena LLCCamarillo, CA
Onsite

About The Position

Hygiena provides rapid microbiology diagnostic tests and solutions for mission-critical, time-sensitive processes around the world. Hygiena’s proprietary diagnostic technologies enable customers to; prevent illness and save lives, comply with regulations, protect products and brands, run businesses more effectively. At Hygiena we believe in providing the highest quality products & service, being a leader in innovation, having a compelling desire to improve and win in the marketplace, and in contributing positively not only in the workplace, but in our community and environment. With rapid growth comes opportunity. We are looking for a QC Inspector I to join our team in Camarillo, CA. This is a non-exempt position. The QC Inspector will be responsible for performing receiving inspections of raw materials and components, in addition to conducting in-process and final inspections during production to verify compliance with quality procedures, product specifications and all relevant regulatory standards (ISO 9001, ISO 13485, FDA, USDA).

Requirements

  • High school diploma or GED equivalent required.
  • Minimum 2 years’ Quality Control Inspector experience.
  • Knowledge in using measuring tools such as calipers, gauges, micrometers and force gauges required.
  • Knowledge of Microsoft Office (Outlook, Word, Excel, Visio, PowerPoint) and Adobe Acrobat required.

Nice To Haves

  • Knowledge of Microsoft Navision Dynamics system is a plus
  • Bilingual Spanish preferred, but not required

Responsibilities

  • Performs in-process inspections on the manufacturing floor to ensure products meet specifications per Manufacturing Procedures (MPPs)/Quality Assurance Procedures (QAPs).
  • Documents data and completes batch records as appropriate.
  • Completes Receiving Inspection of various raw materials/components from outside suppliers per purchasing specifications using sampling plans per ANSI/ASQ Z1.4. Identifies and control non-conforming materials.
  • Ensure batch records have proper documentation by maintaining complete identification and traceability per QMS requirements. Performs finalization of batch records and visual inspection of final goods to meet specified requirements.
  • Maintains expertise in the Material Review Board (MRB) process and related documentation. Completes the Material Review Record for nonconforming products and processes; ensure non-conforming materials are quarantined.
  • Issues appropriate COCs and COAs for products shipped, as required. Upload the certificates for multiple product lines (Hygiena, Qualicon, Allergen, Innovate, etc.) to the designated site.
  • Implements at least one improvement idea a year on process simplification and harmonization related to QC processes and forms.

Benefits

  • 15 days of PTO & 10 paid company holidays
  • Medical with HSA employer contribution, Dental, Vision available 1st of the month after start date
  • Company paid Life Insurance, Short and Long-Term Disability and an Employee Assistance Program
  • 401(k) with Safe Harbor and Profit-Sharing employer contributions
  • Tuition Reimbursement program
  • Charitable Contribution matching
  • Employee Referral bonus opportunities
  • State paid short-term disability for California based employees
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service