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Quality Assurance Production Jobs (NOW HIRING)

Tulkoff Food Products

Food Products is a dynamic and rapidly growing private equity-backed portfolio company within the ... The QA Supervisor serves as a key liaison between Quality Assurance, Production, Sanitation ...

Manpower

Quality Assurance

Tonawanda, NY · On-site

$26.47/hr

As a Quality Assurance team member, you will be supporting the QA & Product Safety department. The ideal candidate will demonstrate attention to detail, effective communication skills, and a ...

New

US0767 PRYSMIAN CABLES AND SYSTEMS USA LLC

$25 - $38/hr

The Quality Assurance Technician Lead ensures product compliance at the point of production, data analysis, and support for root cause investigations. This is achieved by auditing processes, hands-on ...

acme

Technician - Quality Assurance

New York, NY · On-site

$20 - $26.50/hr

The QA Technician I will assist the Quality Assurance Department and Manager in executing quality ... Monitor product quality, food safety, packaging, labeling, and production processes to ensure ...

acme

Technician - Quality Assurance

New York, NY

$20 - $26.50/hr

The QA Technician I will assist the Quality Assurance Department and Manager in executing quality ... Monitor product quality, food safety, packaging, labeling, and production processes to ensure ...

Acme

Technician - Quality Assurance

Brooklyn, NY · On-site

$20 - $26.50/hr

The QA Technician I will assist the Quality Assurance Department and Manager in executing quality ... Monitor product quality, food safety, packaging, labeling, and production processes to ensure ...

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How much do quality assurance production jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for quality assurance production in the United States is $44.87, according to ZipRecruiter salary data. Most workers in this role earn between $36.54 and $54.57 per hour, depending on experience, location, and employer.

What is quality assurance production?

Quality Assurance (QA) in production refers to the systematic process of ensuring that manufactured products meet defined quality standards and specifications. QA professionals monitor the production process, conduct inspections, and implement testing procedures to identify defects or deviations from standards. Their goal is to prevent errors, improve product reliability, and ensure customer satisfaction by delivering consistent, high-quality goods. QA in production also involves maintaining documentation and working with other departments to resolve quality issues.

What are common challenges faced by quality assurance production professionals, and how can they address them?

Quality Assurance Production professionals often encounter challenges such as tight production deadlines, balancing product quality with operational efficiency, and managing cross-functional communication. Addressing these challenges involves proactive planning, maintaining clear documentation, and leveraging quality management systems to monitor processes. Regular collaboration with production, engineering, and supply chain teams also helps ensure that any issues are identified early and resolved efficiently, supporting both quality standards and production targets.

What are the key skills and qualifications needed to thrive as a quality assurance production professional, and why are they important?

To thrive in Quality Assurance Production, you need a strong understanding of quality control processes, attention to detail, and familiarity with industry standards, often backed by a relevant degree or certification. Experience with quality management systems (QMS), statistical process control (SPC), and tools like Six Sigma or ISO standards is highly valued. Excellent problem-solving, communication, and teamwork skills set top performers apart in this role. These competencies are crucial for ensuring product consistency, reducing defects, and maintaining compliance in a production environment.

What is the difference between Quality Assurance Production vs Quality Control Inspector?

AspectQuality Assurance ProductionQuality Control Inspector
Primary FocusPreventing defects through process improvements and standardsIdentifying defects through product inspection
Work EnvironmentCollaborates with production teams, involved in process developmentPerforms inspections on finished or in-process products
CertificationsOften requires ISO or Six Sigma certificationsMay require specific industry certifications or training
Employer & Industry UsageUsed across manufacturing, aerospace, automotive sectorsCommon in manufacturing, electronics, and consumer goods

While both roles aim to ensure product quality, Quality Assurance Production focuses on preventing defects through process improvements, whereas Quality Control Inspector emphasizes detecting defects through product inspections. Understanding these differences helps organizations assign the right responsibilities for quality management.

Is quality assurance production a stressful job?

Quality assurance production roles can be stressful due to strict quality standards, tight deadlines, and the need for attention to detail. Employees often perform repetitive tasks and must quickly identify and resolve issues to ensure product quality, which can contribute to job pressure.

What cities are hiring for Quality Assurance Production jobs?

Cities with the most Quality Assurance Production job openings:

What states have the most Quality Assurance Production jobs?

States with the most job openings for Quality Assurance Production jobs include:

What are popular job titles related to Quality Assurance Production jobs?

For Quality Assurance Production jobs, the most frequently searched job titles are:

Quality Assurance Production jobs near you
Infographic showing various Quality Assurance Production job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $93,338 per year, or $44.9 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 yesterday

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.

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