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Artius Solutions

QA Manufacturing Inspector

Fall River, MA · On-site

$17K - $18K/yr

Job Title: QA Manufacturing Inspector - 2nd Shift Job Location: Fall River, MA (On-site) Job Type: Full-Time | Non-Exempt Shift Timing: Second Shift | 03:00 PM - 11:30 PM (flexible as per business ...

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ARTHREX

Senior Engineer - QA Manufacturing

Ave Maria, FL

$79K - $107K/yr

Senior Engineer - QA Manufacturing Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for ...

Arthrex

Senior Engineer - QA Manufacturing

Ave Maria, FL · On-site

$79K - $107K/yr

Senior Engineer - QA Manufacturing Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for ...

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How much do qa manufacturing jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for qa manufacturing in the United States is $52.71, according to ZipRecruiter salary data. Most workers in this role earn between $44.95 and $59.62 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Qa Manufacturing position, and why are they important?

To thrive as a QA Manufacturing professional, you need a solid understanding of quality assurance principles, manufacturing processes, and experience with inspection techniques, usually supported by a degree or certification in a relevant technical field. Familiarity with quality management systems (like ISO 9001), statistical process control (SPC), and tools such as calipers, micrometers, and ERP software is highly advantageous. Attention to detail, strong problem-solving abilities, and effective communication skills are crucial soft skills for this role. These attributes ensure the consistent production of high-quality products, improve process efficiency, and facilitate effective teamwork.

What is a QA Manufacturing job?

A QA Manufacturing job involves ensuring that products meet quality standards and regulatory requirements during the manufacturing process. Responsibilities typically include inspecting materials, monitoring production, conducting tests, and identifying defects or process improvements. QA professionals work closely with production teams to maintain consistency and compliance with industry standards. Their goal is to prevent defects, reduce waste, and enhance overall product quality before reaching customers.

What are some common challenges faced in a QA Manufacturing role?

Common challenges in QA Manufacturing include identifying and correcting process inconsistencies, managing strict production deadlines, and ensuring compliance with company and regulatory quality standards. You may frequently interact with cross-functional teams such as production, engineering, and supply chain to troubleshoot quality issues or implement process improvements. Staying up to date with evolving technologies and standards, as well as adapting to changing product requirements, is essential for long-term success. Overcoming these challenges not only enhances product reliability but also contributes to a more efficient and collaborative workplace.

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Qa Manufacturing jobs near you
QA Manufacturing Inspector

QA Manufacturing Inspector

Artius Solutions

Fall River, MA • On-site

$17K - $18K/yr

Full-time

Posted 18 days ago

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Job description

Job Title: QA Manufacturing Inspector – 2nd Shift

Job Location: Fall River, MA (On-site)
Job Type: Full-Time | Non-Exempt
Shift Timing: Second Shift | 03:00 PM – 11:30 PM (flexible as per business needs)
Industry: Pharmaceutical Manufacturing
Experience Required: 3–15 Years
Relocation: Not Available
Remote Option: Not Available
Travel: Not Required

Job Overview:

We are currently hiring a Quality Assurance Inspector to join our manufacturing quality operations team. This individual will ensure that manufacturing practices and product quality meet required standards during all production phases. The role involves floor-level inspection, testing, and documentation in alignment with cGMP and internal SOPs.

Key Responsibilities:

  • Conduct routine in-process quality checks such as weight, hardness, thickness, disintegration, friability, etc.

  • Perform room and equipment clearance inspections before and after production stages.

  • Execute sampling and inspections based on Acceptable Quality Limits (AQL).

  • Collect product samples for quality testing and ensure proper documentation for lab submissions.

  • Maintain verification logs of balances, weights, and instruments used during inspections.

  • Manage segregation and documentation of rejected batches/materials.

  • Monitor environmental conditions across manufacturing areas.

  • Assist in reviewing equipment calibration, pest control records, temperature logs, and maintenance reports.

  • Review production documentation for completeness and ensure yields/reconciliation accuracy before moving to next steps.

  • Perform complaint sample testing and submit detailed reports.

  • Report deviations, discrepancies, or non-compliance issues to QA leadership.

  • Participate in assigned improvement projects or additional QA activities as needed.

Required Qualifications:

  • Minimum Education: High school diploma required; vocational training or associate degree in pharma or industrial production preferred.

  • Experience: At least 3 years in a GMP-regulated pharmaceutical manufacturing QA role.

  • Dosage Forms: Preferred exposure to inhalation products (MDI); experience with tablets, capsules, liquids, and solids also acceptable.

  • Systems & Tools: Working knowledge of Microsoft Office, ERP (e.g., SAP), and documentation practices.

  • Communication: Must be fluent in spoken and written English.

  • Compliance: Strong understanding of current Good Manufacturing Practices (cGMPs) and standard operating procedures (SOPs).

Desired Skills:

  • High attention to detail with ability to multitask and manage timelines.

  • Strong communication, organizational, and documentation skills.

  • Ability to work independently with minimal supervision on the production floor.

  • Team-oriented mindset and willingness to support cross-functional operations.

Note:
Candidates must have a pure pharmaceutical manufacturing background (not biotech).
Experience with MDI is a strong plus but not mandatory. Candidates with experience in other dosage forms such as solids, liquids, tablets, or capsules will be considered.