1

In Process Inspector Jobs in South Carolina (NOW HIRING)

Additionally, the inspector will support in-process, material receipt, and pre-shipping inspections with broad criteria covering cleanliness, dimensional conformance, verification of material ...

Additionally, the inspector will support in-process, material receipt, and pre-shipping inspections with broad criteria covering cleanliness, dimensional conformance, verification of material ...

Additionally, the inspector will support in-process, material receipt, and pre-shipping inspections with broad criteria covering cleanliness, dimensional conformance, verification of material ...

Machinist Inspector

Summerville, SC · On-site

$32 - $46/hr

Additionally, the inspector will support in-process, material receipt, and pre-shipping inspections with broad criteria covering cleanliness, dimensional conformance, verification of material ...

Machinist Inspector

Summerville, SC · On-site

$32 - $46/hr

Additionally, the inspector will support in-process, material receipt, and pre-shipping inspections with broad criteria covering cleanliness, dimensional conformance, verification of material ...

next page

Showing results 1-20

In Process Inspector information

What is an in process inspector?

In Process Inspectors are quality control professionals responsible for monitoring and evaluating products during various stages of the manufacturing process. Their main duties include inspecting materials, components, and assemblies to ensure they meet specified standards and identifying any defects or deviations. By detecting issues early, they help maintain product quality, reduce waste, and ensure compliance with industry regulations. In Process Inspectors typically use a variety of measuring tools and follow detailed checklists or quality protocols. Their work is essential for delivering reliable and safe products to customers.

What are the key skills and qualifications needed to thrive as an in process inspector?

To thrive as an In Process Inspector, you need a strong understanding of quality control, manufacturing processes, and attention to detail, typically supported by a high school diploma or technical certification. Familiarity with measurement tools, inspection equipment, and quality management systems like ISO standards is essential. Strong observational skills, effective communication, and problem-solving abilities help inspectors identify and address production issues efficiently. These skills ensure products meet quality standards, reduce defects, and maintain smooth production workflows.

What are the main challenges an in process inspector may face during daily inspections?

In Process Inspectors often encounter challenges such as maintaining attention to detail while inspecting repetitive parts, managing time efficiently to meet production deadlines, and ensuring clear communication with production teams when defects are found. Adapting to evolving quality standards and learning new inspection technologies can also be demanding. However, most companies provide ongoing training and encourage teamwork, which helps inspectors stay updated and resolve issues collaboratively.

What is the difference between In Process Inspector vs Quality Control Inspector?

AspectIn Process InspectorQuality Control Inspector
CertificationsOften requires inspection or quality assurance certificationsTypically requires similar certifications, such as ASQ certifications
Work EnvironmentInspects products during manufacturing process on the production lineInspects finished products or during various stages of production
Industry UsageCommonly used in manufacturing, aerospace, automotive industriesWidely used across manufacturing, electronics, and consumer goods sectors

In Process Inspectors focus on monitoring products during manufacturing to catch issues early, while Quality Control Inspectors often evaluate finished products to ensure they meet quality standards. Both roles require similar certifications and are integral to quality assurance in manufacturing industries.

What are popular job titles related to In Process Inspector jobs in South Carolina?

For In Process Inspector jobs in South Carolina, the most frequently searched job titles are:

What cities in South Carolina are hiring for In Process Inspector jobs?

Cities in South Carolina with the most In Process Inspector job openings:

Infographic showing various In Process Inspector job openings in South Carolina as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

In Process Quality Assurance Auditor

TekSky

Greenville, SC • On-site

Full-time

Re-posted 12 days ago


Job description

Job Summary
The In Process Quality Assurance Auditor ensures consistent product quality through independent inspection in process testing, verification and auditing of pharmaceutical drugs during manufacturing and packaging within a cGMP-regulated pharmaceutical manufacturing environment.
This position provides intermediate-level Quality Assurance support across manufacturing, warehousing and packaging operations. The In Process Quality Assurance Auditor applies critical thinking, analytical reasoning, and sound judgment to evaluate data, identify deviations, and ensure compliance with internal procedures and regulatory requirements (FDA, DEA).
Essential Duties And Responsibilities
Quality Assurance Operations
  • Promote and ensure compliance with current Good Manufacturing Practices (cGMPs) and all applicable regulatory standards.
  • Independently perform in-process inspections throughout manufacturing and packaging operations to verify conformance to specifications.
  • Conduct verification of production operations and environmental conditions prior to line clearance and batch initiation.
  • Perform in-process testing (pH, specific gravity, etc.) and assay calculations for compounding operations.
Review batch records, logbooks, and associated documentation for completeness and compliance as the process is in production ; verify data accuracy and documentation integrity. Identify out of trends or non conformances from documented data or auditing on the line from in process testing results , review of label print and application, DSCSA serialization/aggregation , downtime activities, and proactively communicate to put in corrective actions prior to the product being removed from the area. Record inspection results and maintain accurate data in quality systems (SAP, WMS, and other databases).
  • Identify, segregate, and document non-conforming events on the process line, and halt the processing if critical compliance activities are identified. Ie, product spills, equipment set up incorrectly, label print incorrect, mixed components on the line,
  • Immediately escalate non conformance or observations to management for direction
Initiate non conformances in TrackWise system and assist in investigations Apply critical thinking to evaluate quality data, assess deviations, and determine appropriate actions or escalation.
  • Support Process Issues (PIs) and Corrective and Preventive Actions (CAPAs) by providing detailed, factual information.
  • Collaborate with manufacturing and packaging personnel to resolve quality issues and ensure adherence to quality standards.
  • Participate in continuous improvement activities to enhance product quality and operational efficiency.
  • Conduct packaging room and line clearance inspections prior to production start-up.
  • Verify reconciliation of components after batch completion and ensure proper documentation and return to inventory.
  • Exercise judgment and problem-solving skills to identify potential quality risks in packaging operations.
Continuous Improvement and Compliance
  • Support the development and revision of SOPs, Work Instructions (WIs), and related quality documents.
  • Assist with internal audits and data collection for quality reporting.
  • Provide on-the-job training to QA Inspector I or new team members as assigned.
  • Maintain up-to-date knowledge of cGMPs, regulatory requirements, and company quality policies.
Education And Experience
  • High school diploma or GED required; associate degree in a scientific or technical discipline preferred.
  • Minimum 2 years of Quality Assurance or Quality Control experience in a pharmaceutical or regulated manufacturing environment required.
  • Demonstrated understanding of FDA/DEA regulations, cGMP compliance, and documentation practices.
  • Proficiency with Microsoft Office (Word, Excel, Outlook) and experience with SAP or equivalent ERP/WMS systems preferred.
  • Strong mathematical aptitude and ability to perform precise calculations and data entry.
Knowledge, Skills & Abilities
  • Advanced critical thinking and analytical reasoning skills - able to evaluate data, identify trends, and make quality-based decisions.
  • Strong attention to detail, accuracy, and documentation discipline.
  • Excellent communication skills, both verbal and written.
  • Ability to manage multiple priorities and work effectively under minimal supervision.
  • Strong interpersonal skills with the ability to work collaboratively across departments.
  • Self-motivated, dependable, and demonstrates high ethical and professional standards.
Physical Requirements & Working Conditions
  • Regularly required to stand, walk, sit, talk, and hear.
  • Occasionally required to climb, balance, stoop, kneel, crouch, or crawl.
  • Must be able to lift up to 50 lbs.
  • Visual requirements include close, distance, color, and depth perception.
  • Work is performed in both office and manufacturing environments with exposure to moving mechanical parts and occasional contact with chemicals.
  • Must comply with gowning and cleanroom entry requirements.
  • Moderate noise level typical of manufacturing environments.