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QA Inspector, GMP & FDA Compliance in Pharmaceutical Manufacturing

48K–56K
Onsite · Philadelphia, Pennsylvania
Posted August 14, 2026
full-time

Overview

QA Inspector role focused on in-process and final inspections on production and packaging floors in a GMP regulated facility. Own real-time quality oversight to ensure ALCOA+ data integrity and regulatory compliance. Collaborate with Production, Engineering, and Quality teams to resolve issues and drive quality improvements. This position offers on-site work in Philadelphia with competitive benefits and growth opportunities.

What You'll Do10

  • 1Build and perform in-process inspections and line clearances per approved SOPs and batch records to ensure product conformance
  • 2Monitor manufacturing and packaging operations to maintain cGMP compliance and internal quality procedures
  • 3Inspect raw materials, in-process samples, finished products, and labeling against specifications
  • 4Review batch production, cleaning, and packaging records for accuracy and compliance prior to QA release
  • 5Document inspection results, deviations, and nonconformances with contemporaneous accuracy
  • 6Assist with deviation investigations, CAPAs, and quality event documentation under QA management direction
  • 7Support audits, internal inspections, and continuous improvement initiatives
  • 8Collaborate with Production, Engineering, and Quality to address quality concerns promptly
  • 9Maintain data integrity and ensure documentation meets ALCOA+ principles at all times
  • 10Perform related QA responsibilities to meet departmental objectives

Requirements10

  • 11–3 years of Quality Assurance or Quality Control experience in a GMP regulated pharmaceutical, biotechnology, or related manufacturing environment
  • 2High school diploma or equivalent required; Associate degree or coursework in Life Sciences, Chemistry, or related discipline preferred
  • 3Strong understanding of cGMP and FDA compliance requirements
  • 4Knowledge of quality inspection techniques, sampling methods, and documentation review
  • 5Experience with batch record review, line clearance, or in-process inspection preferred
  • 6High attention to detail with the ability to detect and resolve nonconformances
  • 7Proficiency in Microsoft Office (Word, Excel, Outlook) and standard documentation systems
  • 8Excellent written and verbal communication skills across teams
  • 9Strong time-management, organization, and follow-through abilities
  • 10Ability to work independently while maintaining high accuracy and accountability

Salary Insight

$48 - $56k per year

Location

Typeonsite
LocationPhiladelphia, Pennsylvania

Required Skills

cGMPFDA compliancequality inspection techniquessampling methodsdocumentation reviewbatch record reviewline clearanceMicrosoft OfficeWordExcelOutlookwritten communicationverbal communicationattention to detailtime-managementorganizationindependent work
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