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Temporary Qualcomm Qa Jobs (NOW HIRING)

Jobsbridge

QA Manager

Kenosha, WI

Max Salary $ DOE Per Hour Employment Type Contract Jobs (Temp/Consulting) Job Duration 12+ Months Domain Any Description Drive quality assurance (QA) efforts for IT Project Services team. Collaborate ...

Aston Carter

Quality Assurance

Bettendorf, IA · On-site

$29 - $31/hr

Quality Assurance Specialist As a Quality Assurance Specialist, you will be responsible for ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

TRC Talent Solutions

QA Coordinator

Johns Creek, GA

$20 - $24/hr

Temp-to-Hire Position Summary TRC Talent Solutions is seeking a QA Coordinator for a growing electronics manufacturing company in Suwanee, GA. This role will support quality assurance activities ...

Aston Carter

Quality Assurance

Bettendorf, IA

$29 - $31/hr

Quality Assurance Specialist As a Quality Assurance Specialist, you will be responsible for ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

E*Pro, Inc.

Quality Assurance Architect

New York, NY

... Temp-to-Hire. In addition, our industry expertise and knowledge within financial services ... Quality Assurance Job Location: New York, NY Job Type: Permanent Full Time Description: * A strong ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · On-site

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst Newspapers

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

Hearst

Lead QA Engineer (TEMPORARY)

Chicago, IL · Hybrid

$69 - $81/hr

About this job As a iCrossing QA Lead, you'll lead a test team consisting of manual and automation engineers for one of our biggest clients. You will have an opportunity to lead a QA team and the QA ...

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Temporary Qualcomm Qa information

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$12

$29

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How much do temporary qualcomm qa jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for temporary qualcomm qa in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is the difference between Temporary Qualcomm Qa vs Temporary Qualcomm Tester?

AspectTemporary Qualcomm QaTemporary Qualcomm Tester
CertificationsRelevant QA certifications, such as ISTQBBasic testing certifications or experience
Work EnvironmentOffice and lab settings, focusing on quality assurance processesLab and production environments, focusing on product testing
Job FocusDeveloping and executing test plans, ensuring quality standardsPerforming tests on hardware/software, identifying defects
Industry UsageCommonly used in tech and semiconductor industriesUsed in electronics and device manufacturing sectors

Temporary Qualcomm Qa roles primarily focus on quality assurance processes, including test plan development and process improvement, often requiring QA certifications. Temporary Qualcomm Testers concentrate on executing tests on devices or software, identifying defects, and working in lab environments. Both roles are essential in tech manufacturing but differ in their specific responsibilities and skill requirements.

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Temporary Qualcomm Qa jobs near you
Infographic showing various Temporary Qualcomm Qa job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 3% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $60,925 per year, or $29.3 per hour.

QA Assistant Temp.

Charles River Laboratories, Inc.

Charleston, SC • On-site

$21/hr

Full-time, Temporary

Medical, Retirement, PTO

Posted 28 days ago

Charles River Laboratories rating

8.3

Company rating: 8.3 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.

Job Overview

This is a temporary opportunity expected to last up to 6 months. The Quality Assurance (QA) Assistant is an entry level trainee position. The QA Assistant will perform audits of incoming and in-process materials, process documentation and labeling to assure accuracy and compliance with Good Manufacturing Practice (GMP) Regulations and Standard Operating Procedures (SOP).

The working hours for this role are Mon-Fri 8:30am-5:00pm.

ESSENTIAL DUTIES AND RESPONSIBILITIES: 
Under the training, mentorship and review of senior Quality Assurance personnel, learn and apply the principles of GMP compliance to work assignments including:
•    Provide administrative assistance and support of Quality Assurance (QA) as needed.
•    Perform raw data audits of documentation for temperature, humidity, and magnehelic gauges monitoring environmentally controlled areas, and autoclave/oven charts to ensure accuracy and compliance with applicable GMPs and Standard Operating Procedures.
•    Review incoming raw material receipt packages for compliance with the requirements detailed in material specifications and applicable testing procedures.
•    Review accessory product records for compliance with the requirements detailed in product specifications and applicable testing procedures.
•    Review instrument release packages for compliance with the requirements detailed in product specifications and applicable testing procedures. 
•    Utilize company provided software to monitor and release materials.
•    Perform all other related duties as assigned.

Qualifications

•    Education: Associate’s degree (A.S./A.A.) or equivalent, preferably in a life science or related discipline.
•    Experience: Entry level - 0+ year experience
•    An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
•    Certification/Licensure: N/A
•    Other:  Knowledge of Microsoft Office ® applications and spreadsheet programs such as Access and Excel. This position requires the individual to comprehend regulations and guidance documents and apply critical thinking skills to evaluate requirements and effectively communicate (written and oral) findings.

The pay for this position is $21.00 per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location.

About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.


About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.

With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.

At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.

We’re committed to providing benefits that elevate your quality of life.  Based on your position these may include:  bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.

Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.

It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.

For more information, please visit www.criver.com.

What Charles River Laboratories employees say

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About Charles River

Sourced by ZipRecruiter

Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Wilmington, MA, US

Year founded

1947

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