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Perrigo Company plc

Packaging QA Technician – 3rd Shift

Perrigo Company plc

. Respond to quality events . Complete related documentation . Determine immediate physical containment and remediation . Assist in identifying, assessing, and containing defects . Conduct ASPs . Manage the rework

Posted 10/9/2026full-timeAllegan • Michigan • United StatesJuniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in cGMP compliance and quality event response within FDA regulated environments, with strong analytical and communication skills to effectively manage documentation and rework processes.

Highest-signal resume keywords
CGMP ComplianceQuality Event ResponseFDA Regulated Industry ExperienceAnalytical SkillsSOP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality Event DocumentationDefect ContainmentRework Process ManagementASPs ConductingManufacturing Process Understanding
Soft Skills
Clear Direction ProvidingOral CommunicationWritten CommunicationInterpersonal SkillsIndependent Work
Industry Keywords
FDA RegulationsCGMP RequirementsSOPsQuality AssuranceManufacturing Compliance

About the role

Key responsibilities & impact
  • Respond to quality events
  • Complete related documentation
  • Determine immediate physical containment and remediation
  • Assist in identifying, assessing, and containing defects
  • Conduct ASPs
  • Manage the rework process, including providing rework instructions
  • Review documentation as necessary
  • Audit Perrigo manufacturing and packaging processes for compliance with applicable cGMP requirements

Requirements

What you’ll need
  • High school diploma or GED is required
  • Advanced education (2-year or 4-year degree, or progress toward a degree) preferred
  • At least 6 months of experience working in an FDA regulated industry required
  • A minimum of 2 years of experience working in an FDA regulated industry preferred
  • Understanding of and ability to apply cGMPs
  • Working knowledge of SOPs
  • Ability to provide clear direction and interpretation
  • Strong analytical skills
  • Excellent oral and written communication skills
  • Strong interpersonal skills
  • Ability to work independently against multiple deadlines
  • Ability to understand equipment operation and manufacturing/packaging processes
  • All application materials, including resumes and CVs, must be submitted in English

Benefits

Comp & perks
  • Competitive compensation
  • Benefits tailored to supporting you and your family
  • Career development opportunities
  • Inclusive, collaborative culture
  • Equal opportunity employment