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Manufacturing Quality Technician

Insight Global

Reno, NVJobSeen 1 day agoSeen in employer's feed 1 day ago

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At a glance

Compensation
No compensation found
Location
Reno, NV
Work Authorization
Not specified

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Job overview

Insight Global seeks a Manufacturing Quality Technician for a biotechnology and medical device firm. The role involves inspecting, processing, and verifying diagnostic components, ensuring compliance with quality and production standards, and supporting continuous improvement while adhering to ISO and regulatory requirements.

Skills & qualifications

RequiredNice to have

Skills

Attention to DetailMicrosoft OfficeQuality InspectionISO-Regulated EnvironmentScientific Bench WorkLaboratory TechniquesAssemblyProduction Operations

Qualifications

High School Diploma or GEDAssociate Degree or Coursework in Biology Chemistry Biotechnology Medical Laboratory Science or Related Field2+ Years Experience in Manufacturing Production Quality Control Laboratory Operations Medical Device Biotechnology Pharmaceutical or Related Industries

Full job description

Job Description

Insight Global is seeking a Manufacturing Quality Technician to join a growing biotechnology and medical device organization. This individual will inspect, process, and verify components used in diagnostic products while ensuring compliance with quality and production standards.

The ideal candidate is detail-oriented, enjoys hands-on work, and can consistently follow established procedures while identifying potential defects and process improvements.

Day-to-Day Responsibilities: Perform detailed inspections of glass and production components to identify defects, contamination, damage, or non-conformances.

Clean, prepare, coat, label, and process materials according to established manufacturing procedures.

Execute production protocols with strict adherence to quality and regulatory requirements.

Conduct quality control checks throughout the manufacturing process.

Document inspection and production activities accurately and completely.

Support engineering, manufacturing, and quality teams with process improvement initiatives.

Ensure compliance with ISO standards, quality systems, and company procedures.

Identify potential failure points and communicate concerns before they impact product quality.

Skills and Requirements

High school diploma or GED.

2+ years of experience in manufacturing, production, quality control, laboratory operations, medical device, biotechnology, pharmaceutical, or related industries.

Exceptional attention to detail and ability to identify small inconsistencies or defects.

Experience following detailed procedures, work instructions, or production protocols.

Basic Microsoft Office proficiency. Experience in medical device, biotech, pharmaceutical, diagnostics, laboratory, veterinary research, or highly regulated manufacturing environments.

Prior quality inspection or quality assurance experience.

Experience working within an ISO-regulated environment.

Associate degree or coursework in Biology, Chemistry, Biotechnology, Medical Laboratory Science, or a related field.

Experience with scientific bench work, laboratory techniques, assembly, or production operations.

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].

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