58538BRQuality InspectorDiazyme PowayCalifornia
Diazyme laboratories, Inc., is a cGMP and ISO 13485 certified medical device manufacturer (www.diazyme.com). Diazyme uses its proprietary enzyme technologies to develop diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. The products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes.
We currently have an exciting opportunity for a Quality Inspector located in Poway, CA (San Diego area). This person will join a multidisciplinary Quality team focusing on diagnostic product quality assurance.
Under general supervision, this position is responsible for inspecting raw material parts, labels, sub-assemblies, equipment, and finished goods to ensure compliance with company specifications, and quality requirements. Sets up, operates, inspects, , parts, subassemblies and finished goods for conformance to specifications. Maintains records, processes, and updates confidential and sensitive electronic and hard copy reports, records and statistics.
DUTIES AND RESPONSIBILITIES:
We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply.
Typically requires a high school diploma or equivalent and two or more years of progressive experience in biotechnology, chemical, electrical, mechanical, electromechanical or metrology inspection and calibration.
Must be customer focused and possess:
the ability to read and understand drawings and raw material specifications, and perform basic mathematical computations;
the ability to communicate and interface effectively with all levels of employees;
the ability to interpret routine information and respond to routine issues;
the ability to maintain the confidentiality of sensitive information; and
familiarity with the use of Microsoft office software.
The ability to work independently or in a team environment is essential as is the ability to work extended hours as required.
Experience with FDA, ISO 9001, ISO 13485, quality assurance program requirements, are desirable.
QualityEntry-Level (0-2 years) OnsiteFull-Time Hourly 45,00067,1250% - 25% NoNoNo5238091No5313301410.00.027-Oct-2026Quality Inspector II
| Location | San Diego, CA |
Browse dozens of recruiter approved resume templates, layouts and formats. Choose your favorite and make it your own in minutes.
Free resume templatesImprove your existing resume or start from scratch and create a standout, ATS-friendly resume. Add job-specific content, download and apply.
Resume Builder