Title: Quality Control Technician
Location: Pomona, California
Duration: 12+ Month
Summary
To support QC functions within our Drugs of Abuse test manufacturing facility. The position will primarily focus on incoming, in-process and final QC testing, labeling, document inspection results and enter raw material inventory data to ensure the quality and functionality of manufactured products.
Tasks And 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.
- Document QC test results on QC Testing Form, retain retention samples as needed.
- Familiarity with all aspects of product and be able to identify defects.
- Use Agile to issue Quality Incident (QI) reports; perform root cause investigation and write investigation report.
- Ensure timely release of product.
- Ensure cleanliness of the QC lab.
- May be required to work overtime (may include weekends) as defined by the needs of the department.
- Work effectively and independently. Cooperatively work with others in all matter of the organization.
- Able to prioritize and handle multiple tasks and responsibilities, attention to detail, Performs well under stress.
- Good English written and verbal communication skills. Basic computer proficiency.
- Moderate computer skill and moderate knowledge of MS Excel and MS Word.
- Assist the head of QC department with any necessary tasks and other duties as assigned.
- Carries out duties in compliance with established business policies.
- Demonstrates commitment to the development, implementation and effectiveness of Company Quality Management System per ISO, FDA, and other regulatory agencies.
- 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.
- Perform other duties & projects as assigned.
Preferred Educational Background
- BA/BS degree in chemistry or biology or equivalent experience preferred.
Preferred Experiential Background
- 0-2 years’ experience with FDA Class I/II device or other regulated industry preferred.
- Proficient in spoken and written English
- Excellent interpersonal skills.
- Excellent computer skills including Microsoft Excel, Word, Agile and other ERP systems
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.
