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MFG Documentation Associate; Lighthouse

Job in Chandler, Maricopa County, Arizona, 85249, USA
Listing for: Medivant Healthcare
Full Time position
Listed on 2026-09-23
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, Production QC/QA, QA Specialist - Analyst/Manager
  • Manufacturing / Production
    Regulatory Compliance Specialist, Production QC/QA, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 45000 USD Yearly USD 45000.00 YEAR
Job Description & How to Apply Below

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

MFG Documentation Associate (Lighthouse)

Full Time Chandler, AZ, US

4 days ago Requisition

Salary Range: $45,000.00 To $45,000.00 Annually

Position Summary

The Manufacturing Documentation Associate (Lighthouse) supports environmental monitoring, manufacturing documentation, audit readiness, and coordination of manufacturing activities while ensuring GMP compliance and operational efficiency.

Key Responsibilities

Documentation & Monitoring

  • Monitor environmental conditions through Lighthouse during manufacturing activities.
  • Document and review Lighthouse alarms and batch printouts.
  • Issue, review, and maintain manufacturing documents, logbooks, and forms.

Manufacturing Support

  • Coordinate documentation for visual inspection and packaging operations.
  • Perform assigned tasks as directed by the HOD.

Compliance & Audit Readiness

  • Conduct GEMBA walks and maintain audit readiness across manufacturing lines.
  • Ensure documentation complies with manufacturing and quality requirements.
Qualifications

Required

  • Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or related field.
  • 1-3 years of experience in pharmaceutical manufacturing or documentation.
  • Strong organizational skills and attention to detail.

Preferred

  • Experience with environmental monitoring systems.
  • Knowledge of GMP documentation and audit requirements.
  • Documentation Management
  • GMP Compliance
  • Audit Readiness
  • Attention to Detail
  • Organization & Planning
  • Training Coordination
What Success Looks Like
  • Environmental monitoring and documentation are completed accurately and on time.
  • Manufacturing records remain audit-ready and compliant.
  • Visual inspection and packaging documentation are effectively coordinated.
  • Manufacturing areas consistently meet inspection and compliance standards.
Position Requirements
10+ Years work experience
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