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In Process Inspector Jobs in Tonawanda, NY (NOW HIRING)

Die Cutter Operator - 3rd Shift

Buffalo, NY ยท On-site

$20.50 - $28.50/hr

Follow Quality guidelines for "in-process" inspection * Perform Preventative Maintenance as outlined in PM Program * Assist with Tooling Change-Overs * Clear Machine Jam-Ups * Deliver finished ...

Grinder

Buffalo, NY

$17 - $21/hr

The operator performs setups ranging from basic to advanced, conducts in-process inspections using calibrated gages, and carries out planned preventive and minor corrective maintenance. Key ...

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Press Brake Operator

Clarence, NY ยท On-site

$23 - $25/hr

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Press Brake Operator

Clarence, NY ยท On-site

$23 - $25/hr

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Press Brake Operator

Clarence, NY ยท On-site

$23 - $25/hr

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Determine with Quality Control in-process inspection requirements, gauging and measuring devices. * Monitor production to ensure conformance with process sheet and time standards. * Monitor machine ...

Quality Inspector

Buffalo, NY ยท On-site

$25 - $27/hr

The Quality Inspector plays a critical role in ensuring products meet contractual, regulatory, and ... Process MTRs and document packages. * Prepare contract folders for Authorized Inspector (AI) review.

The Quality Inspector plays a critical role in ensuring products meet contractual, regulatory, and ... Process MTRs and document packages. * Prepare contract folders for Authorized Inspector (AI) review.

The Quality Inspector plays a critical role in ensuring products meet contractual, regulatory, and ... Process MTRs and document packages. * Prepare contract folders for Authorized Inspector (AI) review.

Grinder

Buffalo, NY ยท On-site

$24.33/hr

The operator performs setups ranging from basic to advanced, conducts in-process inspections using calibrated gages, and carries out planned preventive and minor corrective maintenance. Key ...

QUALITY INSPECTOR

Buffalo, NY ยท On-site

$20 - $21/hr

... in internal and external audits * Perform process and inspection audits * Use measurement tools ... such as calipers, scales, gage blocks, fixtures, and 3D measuring devices * Train other team ...

Be Seen First

... in-process inspection of materials and components to assure conformance with specifications. -Report any problems to operations or management to ensure quality; help develop processes as needed for ...

Showing results 21-40

In Process Inspector information

See Tonawanda, NY salary details

$22.9K

$51.4K

$92.6K

How much do in process inspector jobs pay per year?

As of Aug 15, 2026, the average yearly pay for in process inspector in Tonawanda, NY is $51,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,000.00 and $59,400.00 per year, depending on experience, location, and employer.

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 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 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 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 cities near Tonawanda, NY are hiring for In Process Inspector jobs?

Cities near Tonawanda, NY with the most In Process Inspector job openings:

Infographic showing various In Process Inspector job openings in Tonawanda, NY as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 18% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $51,411 per year, or $24.7 per hour.

MQA III (Aseptic Process and Cleanroom Behavior)

Pine Pharmaceuticals

Tonawanda, NY โ€ข On-site

$24 - $28.50/hr

Full-time

Posted 3 days ago

New


Job description

Position Summary:

Responsible for the routine oversight of manufacturing operations to ensure compliance with cGMP, Pine Policies and Procedures, and good aseptic technique.


Essential Functions:

Fully qualified and capable of executing all responsibilities across MQA Specialist level II and the following:

Cleanroom Oversight & Compliance

  • Act as Subject Matter Expert (SME) for aseptic processes and cleanroom behaviors.
  • Conduct routine and non-routine audits of cleanroom suites, including personnel, environment, equipment, and materials.
  • Observe in-process operations to ensure adherence to aseptic technique and process-specific cGMP procedures.
  • Provide real-time feedback and coaching to production operators on aseptic behavior and procedural compliance.
  • Perform real-time and retrospective audits to assess operator technique and compliance with cleanroom standards.
  • Execute aseptic gowning evaluations and support corrective action plans as needed.

Deviation & Nonconformance Management

  • Perform in-process assessments of manufacturing deviations and non-conformances, including risk assessments and immediate corrective actions.
  • Support investigations and time-outs by providing technical expertise in aseptic and cleanroom processes.
  • Audit cleanroom and pre-cleanroom activities in support of investigations.

Training & Cross-Functional Support

  • Act as a compliance resource for other departments, including assistance with deviations, CAPAs, and process-related questions.
  • Collaborate with the training department to identify and remediate operator deficiencies.
  • Provide support and coaching to ensure operator understanding and application of cGMP requirements.

Media Fill & Sterility Assurance Oversight

  • Audit and oversee media fill runs for compliance with aseptic technique and regulatory requirements.

Manufacturing QA Oversight

  • Ensure all components and materials issued for manufacturing are approved, within expiry, and appropriate for intended use.
  • Verify purity calculations for APIs and ensure proper tracking of bulk powder expiration dates.
  • Monitor and verify proper material issuance to batch records and BOMs.
  • Oversee cleanroom material stocking, component staging, and bulk mixing processes.

Material & Component Quality Monitoring

  • Track trends and escalate issues associated with raw materials, container/closure systems, and in-process components.
  • Perform inspections and approvals of reusable components (e.g., glassware, autoclave cycles).

Procedural Compliance & Improvement

  • Routinely evaluate procedural adherence and recommend updates to enhance compliance and efficiency.
  • Verify completion of required processing steps, including log entries and batch record documentation.
  • Audit aseptic cleaning activities and ensure consistency with SOPs and regulatory expectations.

Additional Responsibilities

  • Additional tasks inside and outside the cleanroom as required by management.

Education and Experience:

  • Minimum of two years in aseptic manufacturing/cGMP experience. At least six months must contain bulk formulation experience.
  • Associates degree in a scientific field highly desired.
  • Knowledge of computer software highly desired: Microsoft Word, Excel, Sharepoint, Outlook, MasterControl

Knowledge, Skills and Abilities:

  • Strict attention to detail
  • Quality-based mindset
  • Ability to identify and address deviations from policy and procedure
  • Ability to perform risk-based assessment of events
  • Strong communication skills and ability to advise operators for corrections when deviations are identified
  • Excellent time management and ability to balance multiple responsibilities within the confines of one shift
  • Ability to work independently and as a team
  • Ability to identify process or procedure flaws and propose pathways to improvement (i.e., problem solving skills)