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Hourly Qa Validation Jobs (NOW HIRING)

Company Description Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs ...

Validation QA Specialist

Pomona, CA · On-site

$110K - $120K/yr

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Your Role The Validation QA Specialist is responsible for providing Quality Assurance oversight of validation documentation and ensuring compliance with applicable GMP regulations, company procedures ...

Perform hourly quality inspections on packaging lines. * Complete quality documentation accurately ... Quality Assurance Technician Requirements: * Previous experience working in a food/beverage ...

Showing results 41-60

Hourly Qa Validation information

See salary details

$10

$56

$98

How much do hourly qa validation jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for hourly qa validation in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Qa Validation jobs?

The most popular types of Qa Validation jobs are:

Specialist QA - Validation, cGMP

Aequor

Woburn, MA

Contractor

Re-posted 16 days ago


Job description

Company Description

Engineering

Job Description

Job Title- Specialist QA

Location- Woburn, MA

Duration - 12 months with possible extension

Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs, Change

 Bio-pharma space / Biologics . M-F onsite

    Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of pharmaceutical processes/systems/equipment 
    Project Management and organizational skills, including ability to follow assignments through to completion

Direct: 732-339-3518 - Ext 2065

              

Qualifications

    Bachelor degree in a science or engineering discipline
    No less than 5 years of experience in the pharmaceutical environment and validation

Additional Information

All your information will be kept confidential according to EEO guidelines.