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Quality Control Associate Reagent Manufacturing

Tailored Management

Tucson, AZ

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JOB DETAILS
SALARY
$20–$25.75 Per Hour
SKILLS
Analysis Skills, Biology, Business Support, Calibration, Communication Skills, Continuous Improvement, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Data Analysis, Decision Support, Detail Oriented, Documentation, Environmental Compliance, Environmental Monitoring, Equipment Maintenance/Repair, FDA (Food and Drug Administration), GLP (Good Laboratory Practices), High School Diploma, ISO (International Organization for Standardization), Identify Issues, Inventory Cycle Counts, Inventory Management, Laboratory, Laboratory Equipment, Laboratory Management, Laboratory Operations, Laboratory Techniques, Leadership, Lift/Move 20 Pounds, Lift/Move 25 Pounds, Maintain Compliance, Manufacturing, Manufacturing Operations, Materials Testing, OSHA, Onboarding, Operational Improvement, Operational Strategy, Operations Planning, Operations Processes, Organizational Skills, Performance Analysis, Performance Metrics, Presentation/Verbal Skills, Problem Solving Skills, Procedure Development, Process Improvement, Quality Assurance Methodology, Quality Control, Quality Metrics, Quality System Requirements (QSR), Record Keeping, Regulations, Regulatory Requirements, Reporting Skills, Shipping/Receiving, Staff Training, Standard Operating Procedures (SOP), Team Player, Test Data, Testing, Time Management, Vendor/Supplier Planning, Vision Plan, Writing Skills
LOCATION
Tucson, AZ
POSTED
5 days ago
Role: Quality Control Associate – Reagent Manufacturing
Location: 1910 East Innovation Park Drive, Tucson, AZ 85755
Contract Duration: 12 Months (Potential for Extension or Full-Time Conversion)
Pay Rate: $20.00 – $25.75/hour + Benefits
Benefits: Weekly Pay | Medical | Dental | Vision Insurance
 
Top 3 Desired Skills
  • Strong analytical and problem-solving abilities
  • Excellent communication and organizational skills
  • Ability to lift 20–25 lbs and stand for extended periods
 
Job Summary
We are seeking a detail-oriented Quality Control Associate – Reagent Manufacturing to support raw material and finished goods testing in a regulated manufacturing environment. This role is responsible for quality documentation, data analysis, laboratory compliance, environmental monitoring, and maintaining inspection readiness in accordance with ISO 13485, cGMP, and regulatory standards.
The ideal candidate will thrive in a fast-paced laboratory setting, demonstrate strong technical and troubleshooting skills, and collaborate cross-functionally to support quality and manufacturing operations.
 
Key Responsibilities
Quality Control & Laboratory Operations
  • Perform inspection and testing of raw materials, in-process materials, and finished goods in compliance with established procedures.
  • Record test results, complete batch records, document observations, and generate qualification reports.
  • Analyze test data and support quality decision-making processes.
  • Prepare and maintain compliant QC documentation for Device History Records and product release activities.
  • Maintain laboratory records, equipment, and environment to meet cGMP, operational procedures, and regulatory requirements.
  • Conduct routine laboratory equipment maintenance and support vendor coordination when required.
  • Perform environmental monitoring activities for laboratory and manufacturing areas.
  • Manage laboratory inventory, supply ordering, cycle counts, and inventory control processes.
  • Support reagent formulation activities for testing processes.
Quality, Compliance & Safety
  • Ensure compliance with FDA, OSHA, ISO, QSR, and internal quality standards.
  • Investigate Out-of-Specification (OOS) results and support non-conformance investigations and corrective actions.
  • Maintain calibration compliance for laboratory equipment.
  • Review and provide feedback on document changes and procedural updates.
  • Promote and maintain a strong safety culture by identifying and escalating workplace risks.
  • Maintain complete, accurate documentation and achieve internal training compliance targets.
Continuous Improvement
  • Participate in Lean and 6S initiatives to improve operational efficiency.
  • Support process improvement projects and operational excellence programs.
  • Collect and report performance metrics to support business improvements.
  • Contribute to team meetings and ongoing optimization initiatives.
Collaboration & Team Support
  • Partner with cross-functional teams including vendors, planners, and operational groups.
  • Assist with onboarding and training new employees and contractors.
  • Support quality investigations, product transfers, and technical projects.
  • Update and maintain standard operating procedures (SOPs).
  • Provide backup support for QC leadership when required.
 
Education
  • High School Diploma required
  • Associate’s or Bachelor’s Degree in Science or Life Sciences preferred
 
Experience
  • 7+ years of experience in a regulated industry with a High School Diploma, OR
  • 3+ years of experience with an Associate’s Degree, OR
  • Entry-level opportunity for candidates with a Bachelor’s Degree
 
Required Skills & Qualifications
  • Strong verbal and written communication skills
  • Excellent analytical, troubleshooting, and problem-solving abilities
  • Hands-on laboratory experience
  • Precise pipetting and measurement techniques
  • Strong attention to detail and organizational skills
  • Proficiency with Google Workspace and computer applications
  • Ability to meet deadlines and work collaboratively
  • Experience performing moderate to complex laboratory techniques
 
Preferred Qualifications
  • Experience handling corrosive and biohazardous reagents
  • Experience working in GLP, cGMP, or ISO-regulated environments
  • Familiarity with Lean and 6S methodologies
 
Physical Requirements
  • Work in a controlled environment requiring PPE (gown, hairnet, gloves, safety glasses, foot coverings)
  • Ability to lift and move up to 25 lbs
  • Ability to stand, walk, bend, crouch, and perform repetitive hand movements for extended periods
  • Flexibility to work overtime or shifts based on business needs
#TMN

About the Company

T

Tailored Management

CONNECTING TOP TALENT WITH TOP-TIER OPPORTUNITIES

Tailored Management is a global staffing firm that specializes in partnering with large organizations that run their contingent labor program in a VMS/MSP environment. We have the unique capacity to support programs across all scopes and geographic locations from a single headquarters, successfully elevating program performance across the board and minimizing costs, miscommunication and delivery times. But what do we really do? We bring together the best talent with the greatest opportunities.

COMPANY SIZE
1,000 to 1,499 employees
INDUSTRY
Staffing/Employment Agencies
FOUNDED
1968
WEBSITE
https://www.tailoredmanagement.com/

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