ZipRecruiter

Log In

1

Qa In The Last 3 Days Jobs in Riverside, CA (NOW HIRING)

IEHP

Engineer III - QA

Rancho Cucamonga, CA · On-site

... III - Quality Assurance to lead Quality Assurance efforts on complex software products. The role ... This experience is in addition to the minimum years listed in the Experience Requirements above • ...

LGM Pharma, LLC

SUPERVISOR, QUALITY ASSURANCE

Irvine, CA · On-site

$90K - $105K/yr

Manages or assists in the compliance profile of the site and drives continuous improvements, QRB ... Quality Assurance in a GMP facility, including people management and/or equivalent combination of ...

Philips

Quality Assurance Coordinator

Ontario, CA · On-site

$26 - $41/hr

Job Title Quality Assurance Coordinator Quality Assurance Coordinator As a Quality Assurance ... in-person at least 3 days per week. Onsite roles require full-time presence in the company ...

ontrac

Quality Assurance Consultant

Dallas, TX · Hybrid

$104K - $157K/yr

OnTrac is hiring a Quality Assurance Consultant ! Are you eager to join a dynamic and expanding ... in the U.S. Location: Hybrid - 3 days onsite / 2 days remote. This position may be based in ...

ontrac

Quality Assurance Consultant

Dallas, TX · Hybrid

$104K - $157K/yr

OnTrac is hiring a Quality Assurance Consultant ! Are you eager to join a dynamic and expanding ... in the U.S. Location: Hybrid - 3 days onsite / 2 days remote. This position may be based in ...

Philips

Quality Assurance Coordinator

Ontario, CA · On-site

$26 - $41/hr

Job TitleQuality Assurance Coordinator Quality Assurance Coordinator As a Quality Assurance ... in-person at least 3 days per week. Onsite roles require full-time presence in the company ...

next page

Showing results 1-20

All JobsQa In The Last 3 Days JobsQa In The Last 3 Days Jobs in Riverside, CA

Qa In The Last 3 Days information

See Riverside, CA salary details

$15

$46

$67

How much do qa in the last 3 days jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for qa in the last 3 days in Riverside, CA is $46.82, according to ZipRecruiter salary data. Most workers in this role earn between $38.12 and $56.92 per hour, depending on experience, location, and employer.

What is the difference between Qa In The Last 3 Days vs Qa Analyst?

AspectQa In The Last 3 DaysQa Analyst
CertificationsBasic QA certifications, testing tools knowledgeAdvanced QA certifications, testing methodologies
Work EnvironmentShort-term, project-specific testingOngoing testing, process improvement
Industry UsageFrequent in fast-paced release cyclesCommon in software development companies

Qa In The Last 3 Days typically refers to recent testing activities, often in a short-term context. Qa Analyst involves ongoing quality assurance responsibilities, including process analysis and long-term testing strategies. Both roles require similar skills but differ in scope and duration of tasks.

What are popular job titles related to Qa In The Last 3 Days jobs in Riverside, CA?

For Qa In The Last 3 Days jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Qa In The Last 3 Days jobs in Riverside, CA look for?

The top searched job categories for Qa In The Last 3 Days jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Qa In The Last 3 Days jobs?

Cities near Riverside, CA with the most Qa In The Last 3 Days job openings:

Qa In The Last 3 Days jobs near you
Infographic showing various Qa In The Last 3 Days job openings in Riverside, CA as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 24% Part Time, 1% Temporary, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $97,376 per year, or $46.8 per hour.

Quality Assurance Associate I - 2nd Shift

Irvine, CA • On-site

Siegfried
Civil Engineering Construction • 11 - 50 employees
Learn more about Siegfriedexternal

$30 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Job description

"Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions-offering long-term opportunities to grow and make an impact.

Your Role:

The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release.
2nd Shift Hours: 2 PM - 10:30 PM Monday through Friday

Your Profile:

Responsibilities

QA Production Floor Support

  • Provide Quality support to Manufacturing personnel on the shop floor for compounding and QA- in-process checks.
  • Perform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CSIT/PID test, weight check, and torque test.
  • Perform AQL and Level II Visual Inspection for Finished products.
  • Prepare in-process samples for submission to the Quality Control laboratory. Support handling of GMP events and initiation of deviation investigations.
  • Read, understand, and follow SOP's and comply with cGMP and GDP.
  • Support the issuance of GMP documentation to the Manufacturing floor.

QA Batch Review and Product Release

  • Review executed batch records for completeness, accuracy and compliance with approved procedures and Good Documentation Practices (GDP) and resolve discrepancies with manufacturing operators or supervisors.
  • Use computerized systems and software such as SAP, LIMS, and TrackWise for data collection and batch record review.
  • Enter and verify data from executed batch records into the Product Log Sheet and maintain the database up to date at all times.
  • Participate in deviation investigation and CAPA implementation.
  • Initiate Certificate of Conformance and prepare executed batch records for product release in a timely manner to meet compliance requirements and business needs.
  • Scan and file batch records (physically & electronically).
  • Assist in writing and/or revising SOPs to ensure compliance with cGMP and other applicable regulations.

Required Knowledge, Skills and Abilities

  • Working knowledge of QA principles In Pharmaceutical and/or other FDA regulated industries required
  • Good computer skills
  • Strong attention to detail
  • Good oral and written communication skills
  • Ability to work overtime and/or work
  • on weekend as needed

Required Education and Experience

  • Bachelor's Degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required
  • 1-2 years' experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required

Target Pay Range: $30-32/hour +10% Differential when working on 2nd Shift (2 PM -10:30 PM)

Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.

Your Benefits:

  • Medical, Dental, Vision, Life
  • Voluntary Accident, Hospital, Pet
  • 401K
  • Generous Time Off Structure including PTO, Holidays, Sick & Personal

Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry.

Apply