- Conduct product testing including testing to support complaint investigations and stability verification
- Generate product testing results reports
- Review production batch records DHR's for accuracy and completeness in order to approve intermediate products for use in production. Review finished goods batch records. Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
- Conduct spot-check inspections/audits of production operations
- Participate in the internal audit program
- Write review and approve Standard Operating Procedures SOPs as necessary
- May assist in supporting the Document Control program record retention areas and sample retention areas
- Log returned instruments from the field.
- Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
- Inspect returned instruments for damage and performing basic investigation and documenting results prior to second level processing.
- As necessary process instrument documentation for return to repair facility and pack instruments as required.
- Bachelor's degree in a scientific or technical area or equivalent combination of experience and education. At least one year in quality assurance role in medical device industry is preferred.
- Ability to apply concepts such as fractions percentages ratios and proportions to practical situations.
- To perform this job successfully an individual should have knowledge of Database software Internet software Inventory software Spreadsheet software and Word Processing software.
- Ability to follow procedures and accurately document results
- Understanding the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures
- Attention to detail.
- Ability to use bleach for cleaning purposes is required.
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
Quality Control Technician - Diamond Bar, United States - Actalent
Description
Perform a wide variety of activities to support the Quality Management System.
Essential Duties and Responsibilities:
May support returned instrument processing:
Education and/or Experience:
Mathematical Skills:
Computer Skills:
Other Skills and Abilities:
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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