×
Register Here to Apply for Jobs or Post Jobs. X

Quality Assurance Specialist

Job in Pomona, Los Angeles County, California, 91768, USA
Listing for: Abbott
Full Time position
Listed on 2026-01-04
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below
Position: Quality Assurance Specialist I

Quality Assurance Specialist I – Abbott

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio spans diagnostics, medical devices, nutritionals and branded generic medicines. We serve people in more than 160 countries.

Location:

Pomona, California
. The position is within our CMI Unit.

Benefits
  • Career development with an international company.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan.
  • An excellent retirement savings plan with a high employer contribution.
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit.
  • Recognition as a great place to work worldwide.
  • Recognition for diversity and inclusion.
Responsibilities
  • Responsible for implementing and maintaining the effectiveness of the Quality System.
  • Participate in Quality System processes which may include training, corrective action and preventive action (CAPA) activities, equipment maintenance, product and process planning, quality audits, validation.
  • Aid in implementing process improvements with respect to Quality Assurance processes.
  • Maintain Quality metrics as required.
  • Manage and/or assist with complaints, CAPA, change requests, NCMRs, deviations.
  • Provide support to QA activities for regulatory compliance (i.e. Management Review support, regulatory audits).
  • Assist in determining quality attributes and requirements. May provide technical assistance.
  • Utilize quality management techniques to perform investigations and facilitate solutions.
  • Work with managers to coordinate training requirements for employees as required.
  • Manage training program and organizational chart as required.
  • Perform Quality System Training Requirements as needed.
  • Review/approve supplier surveys and make recommendations as required.
  • Assist with internal audits and agency audits.
  • Manage Document Control as required.
  • Recognizes risks versus the relative gains associated with actions; understands a project's critical success factors and makes recommendations and decisions impacting those factors.
  • Drives functional performance to ensure that cross-functional standards and expectations are met.
  • May assist in the training of personnel as directed by management.
  • Responsible for completing documentation in a timely manner and in accordance with business standards.
  • Manage equipment maintenance and calibration program as required.
  • Assist with equipment, process and facility qualification and validation activities as required.
  • 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.
  • 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.
  • Carries out duties in compliance with established business policies.
  • Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
  • Perform other duties and projects as assigned.
Required Qualifications
  • BS/BA degree in chemistry, biology, or other scientific discipline or equivalent combination of education and work experience.
  • 0-2 years’ experience in Quality Assurance or Regulatory Compliance experience in a manufacturing environment, preferably in vitro diagnostics.
  • 0-4 years of relevant work experience in assigned subsystem(s).
  • Writing and Communication Skills (e.g. write technical reports, present data analysis).
  • Experience with MS Office including excel and power point.
  • Must be detail-orientated, self-motivated and available for flexible scheduling.
Preferred Qualifications
  • Knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485, CMDR.
  • Demonstrated initiative and problem-solving skills.
  • Ability or aptitude to use various types of databases and other computer software.
  • Strong organizational skills.
  • Ability to clearly, concisely and accurately convey…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary