harbaheadercoverblack.png

Senior Quality Engineer - Packaging & Labeling

Indianapolis $125,000 - $150,000 Permanent

Key Responsibilities

  • Provide quality oversight for pharmaceutical packaging, labeling, and serialization operations
  • Support automated and high-speed packaging line activities within a GMP environment
  • Manage investigations, deviations, CAPAs, and change controls related to packaging and labeling events
  • Review and approve SOPs, batch record documentation, and packaging specifications
  • Support validation and qualification activities for packaging equipment and labeling systems
  • Partner cross-functionally with Manufacturing, Engineering, Technical Services, and Supply Chain teams
  • Ensure inspection readiness for FDA, EMA, and client audits
  • Support defect investigations, label reconciliation, and packaging compliance initiatives
  • Drive continuous improvement efforts across packaging quality systems
  • Maintain compliance with serialization and track-and-trace requirements


Qualifications

  • 5+ years of experience in pharmaceutical or biotech Quality Assurance
  • Direct experience supporting packaging, labeling, or serialization operations in a GMP-regulated environment
  • Experience within sterile injectable, biologics, or other highly regulated manufacturing environments preferred
  • Strong understanding of deviations, CAPAs, risk assessments, and validation activities
  • Familiarity with automated packaging technologies and serialization platforms
  • Experience supporting FDA and/or EMA inspections
  • Strong communication skills with the ability to work across multiple departments
Share this job:

Apply now

Similar Jobs

Senior Sustainability Engineer

Boston 137K - 160K Permanent

Job Responsibilities: Shape and execute environmental reduction strategies across multiple company sites, translating high-level corporate commi...

Regulatory Affairs Specialist

St. Louis $44-$47/hr Contract

Key Responsibilities Author, compile, review, and submit regulatory documents in eCTD format, including NDAs, ANDAs, DMFs, and post-app...

Technical Regulatory Affairs Writer

St. Louis $35 - $ 37 /HR Contract

Essential Functions Coordinate regulatory submission projects and support the preparation, compilation, review, and tracking of regulatory docum...

Supplier Quality Engineer

Noblesville $80,000 - $90,000 Permanent

Key Responsibilities Support and maintain the Supplier Quality Program in compliance with applicable regulatory requirements. Perform supplier...

LIMS Administrator

Indianapolis 65 - 80 p/h Contract

Responsibilities Administer, configure, and maintain the LIMS platform, including user access, workflows, test methods, specifications, and inst...