Quality Control Associate , Reagents

Published on:
Oct 7, 2026

Country:
United States

Location:

Austin, Texas

Company:
Luminex Corporation

Job Category:
Operations

Employment type:

Regular Full Time

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

• Build What Matters
  Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
• Innovate with Agility at a Global Scale
  Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
• Grow in a People-Centered Culture
  Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

The Quality Control Associate I, Reagents will be responsible for executing core Quality Control (QC) processes associated with reagent consumable and bioassay production, reagent stability program, and controlled storage monitoring, assisting with incoming quality control, departmental calibration and maintenance and the retention program and maintaining QC laboratory supplies, preparing internal use laboratory reagents, as well as maintaining the integrity and cleanliness of QC work and storage areas.

This position will be participating in QC processes associated with test method development, product development, and equipment/ method validations and have frequent intra-department interaction as well as frequent inter-department interfaces with Quality Assurance, Reagent Manufacturing, Design Transfer and Process Engineering, Production Planning, Purchasing, and Document Control.

Key Duties and Responsibilities

• Deliver timely and accurate Quality Control testing for bioassay and core consumable products.
• Deliver timely and accurate completion of quality control and manufacturing process documentation including related business system transactions.
• Generate Certificates of Quality
• Document and complete non-conformances
• Respond appropriately to environmental monitoring notifications of specialized storage areas; includes 24/7 call list rotation
• Execute stability study sample scheduling and processing.
• Participate in program to sustain orderliness and cleanliness within related quality control and manufacturing area through routing sorting, labeling, systematic cleaning, and standardizing.
• Assist in timely processing of purchased materials for release including related business system transactions.
• Assist in on-time maintenance and calibration of Reagent QC measuring and monitoring devices
• Schedule timely outsource testing and services with associated documentation of results.
• Assist in monitoring of departmental supplies and stocking of focused Reagent QC supplies; generate Purchase orders as needed.
• Assist in filing retentions and retention maintenance program.
• Prepare laboratory reagents for internal use
• Deliver timely and accurate completion of inventory cycle counts for select sub-inventories.
• Participate in applicable departmental and interdepartmental training
• Maintain current training to standard operating procedures, quality control instructions (QCIs), and applicable changes affecting quality control.
• May assist in training of QC Technician and QC Associates to task-specific operations.
• Assist in investigation and resolution of findings impacting Reagent Quality Control initiated through audits, non-conformances, corrective/preventive actions, or customer complaint escalation.
• Assist in the execution of validations of test methods, equipment, and processes.
• Assist in the review or revision of reagent QCIs, manufacturing instructions, and SOPs as required.
• Support design transfer and the integration of new products and processes
• Support process development and process improvement projects.
• Assist in…