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QA Inspector III - 2nd Shift

Job in Orangeburg, Rockland County, New York, 10962, USA
Listing for: PDI
Full Time position
Listed on 2026-01-14
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager, Quality Engineering
  • Manufacturing / Production
    QA Specialist / Manager, Quality Engineering
Job Description & How to Apply Below
Location: Orangeburg

Description

Driven by a commitment to research, quality, and service, PDI provides innovative products, educational resources, training, and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture, and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team!

POSITION

PURPOSE

The Quality Assurance Inspector III ensures that all products manufactured on the production floor meet required quality, regulatory, and customer standards. This role performs daily in-process inspections, testing, documentation review, and line clearances to verify compliance with GMPs and manufacturing specifications. The Inspector collaborates closely with Production and Quality teams to identify discrepancies, support sample collection and rework activities, and assist with trials and validations.

As a senior-level inspector, this position also provides oversight and serves as backup to the Lead QA Inspector, ensuring appropriate coverage of inspection activities and supporting coordination of quality tasks across production lines when needed.

ESSENTIAL FUNCTIONS AND BASIC DUTIES
  • Perform daily inspection of all production lines to assure compliance to GMPs and company. Accurately and completely document all inspection information on Daily Inspection Report (DIR). Documentation required includes but is not limited to: incoming lot #, liquid lot #, item #s, fill weights, defects, etc. Ensure that all manufacturing specifications for components, labeling and product are correct, clear and complete.
  • Inspect work areas for removal of all previous products and components. Verify readiness of work areas prior to use (Line Clearance).
  • Monitor, sample, and inspect in-process finished product for quality by performing appropriate tests. Collect data and samples to support disposition of product. Determine final disposition of products inspected and verify information on transfer tickets. Apply appropriate disposition label to material.
  • Identify and notify Production and Quality when discrepancies from procedures and specifications are observed.
  • Perform AQL inspections as required.
  • Execute Rework protocols as required.
  • Initiate/Login LIMS and Retain Samples.
  • Print Specifications from AS400, create shop order packages, and provide to Production, as needed.
  • Collect samples as required by customers or Nice Pak/PDI specifications and ship samples to customers, as required by the Manufacturing Instructions.
  • Collect stability samples.
  • Execute Trials and Validations.
  • Review documentation to assure accuracy prior to submittal to QA Release team.
  • Review Master Batch Sheets.
  • Act as Lead QA Inspector in his or her absence to complete distribution of lines and ensure proper coverage of the production floor during the appropriate shift.
  • Identify continuous improvement opportunities and promote a quality culture.
  • Handle assignments as requested by supervision to establish and maintain product quality.
  • Perform any required testing as per SOPs and WIs.
PERFORMANCE MEASUREMENTS
  • First time right on review of production jackets
  • On-time completion of all training
QUALIFICATIONS

EDUCATION/CERTIFICATION:
  • Associate's Degree in a scientific, technical, or related field, or equivalent combination of education and experience.
REQUIRED KNOWLEDGE:
  • Strong understanding of Good Manufacturing Practices (GMPs), quality systems, and regulated manufacturing environments.
  • Working knowledge of AQL inspection standards, sampling plans, and in-process quality control methods.
  • Familiarity with batch documentation, manufacturing specifications, and component/label verification.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook); ability to learn and operate quality-related systems such as LIMS, ERP, and electronic documentation tools.
EXPERIENCE

REQUIRED:
  • Minimum 3+ years of experience in a regulated industry (e.g., FDA, EPA, ISO), preferably in manufacturing or quality assurance roles.
  • Demonstrated experience performing in-process quality…
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