Quality Control Technician

Job Title: Quality Control Technician

Location: Pomona, CA

Duration: 8 Months

Responsibilities

• Perform and document incoming, in-process, and final QC testing of in-vitro diagnostics devices to meet compliancy requirements including ISO, FDA and international regulations
• Familiarity with all aspects of product and be able to identify defects
• Cross-train on all processes in QC lab
• May train new staff on processes
• Able to solve process-related questions/problems
• Use Agile to issue quality incidence; perform root cause investigation and write investigation report
• Perform validation study or other appropriate analyses for current or new product/ new features of the product
• Prepare adulteration controls and DOA controls as needed
• Be able to use analytical balance, optical comparator, vacuum chamber, caliper, gauges and the other tools to perform QC testing or measurements
• Ensure timely release of product
• Ensure cleanliness of the QC lab
• Assist the head of QC department with any necessary tasks
• Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities
• Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships
• Carries out duties in compliance with established business policies
• Other duties as assigned, according to the changing needs of the business
  
  

Minimum Qualifications | Education/Experience:

• Requires high school diploma
• Two to five years of laboratory experience
• Ability to follow detailed instructions, maintains accurate records and notes, and carry out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices
• Good written and verbal communication skills
• Experience working in GMP environment
• Intermediate knowledge of a variety of lab equipment and their operation
• Intermediate knowledge of MS Office and manufacturing systems
  
  

Preferred Qualifications

• Experience working with semi-automated equipment
• Medical device manufacturing preferred
• Knowledge of regulations (FDA, ISO, OSHA, etc.)
• Be able to prioritize and handle multiple tasks and responsibilities, attention to details
  
  

Competencies

• Communication
• Attention to detail
• Work in a team environment
  
  

Consultants Eligible Benefits Upon Waiting Period

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account (for High Deductible Health Plans)
• Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
• Supplemental Life Insurance
• Short Term Disability (coverage varies by state)
• Long Term Disability
• Critical Illness, Hospital coverage, Accident Insurance
• MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
• 401(k)
  
  

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.

Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.