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Manufacturing Technician

Job in Chandler, Maricopa County, Arizona, 85249, USA
Listing for: Medivant Healthcare
Full Time position
Listed on 2026-10-11
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Production QC/QA, Quality Engineering
  • Quality Assurance - QA/QC
    Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 52000 - 76000 USD Yearly USD 52000.00 76000.00 YEAR
Job Description & How to Apply Below
Job Posting Title
- Cleanroom Manufacturing Technician

Job Description Position Summary

The Cleanroom Manufacturing Technician supports sterile injectable manufacturing operations by performing aseptic production, filling, compounding, packaging, and documentation activities in a controlled cleanroom environment. This role ensures compliance with FDA regulations, cGMP requirements, USP / standards, and Medivant Healthcare quality procedures while supporting safe, efficient, and compliant manufacturing operations.

Key Responsibilities Manufacturing Operations
  • Perform aseptic manufacturing, compounding, filling, and packaging activities.
  • Operate and monitor manufacturing equipment, including filling machines, autoclaves, and compounding tanks.
  • Prepare materials and equipment for production batches.
  • Maintain cleanroom standards, gowning requirements, and personnel hygiene practices.
  • Support environmental monitoring and routine equipment cleaning.
Documentation & Compliance
  • Complete Batch Manufacturing Records (BMRs), logbooks, and production documentation accurately.
  • Follow Good Documentation Practices (GDP) and cGMP requirements.
  • Maintain manufacturing records in compliance with FDA and company standards.
  • Support audit readiness and inspection activities.
Quality & Team Collaboration
  • Follow all safety, quality, and compliance requirements.
  • Report deviations, equipment issues, and quality concerns promptly.
  • Collaborate with Quality, Operations, and Manufacturing teams to meet production schedules.
  • Participate in training and continuous improvement initiatives.
  • Perform additional duties as assigned.
Qualifications Required
  • High school diploma or GED.
  • Strong attention to detail and commitment to quality.
  • Ability to work in a cleanroom environment and wear required PPE.
  • Strong teamwork and communication skills.
  • Ability to stand for extended periods and lift up to 25 lbs.
Preferred
  • Experience in pharmaceutical manufacturing, sterile compounding, or cleanroom operations.
  • Familiarity with FDA-regulated and cGMP environments.
  • Technical or vocational training in science, healthcare, or manufacturing.
  • Aseptic Processing
  • Cleanroom Operations
  • cGMP Compliance
  • Documentation Accuracy
  • Quality Focus
  • Attention to Detail
  • Teamwork & Communication
  • Safety Awareness
  • Problem Solving
What Success Looks Like
  • Manufacturing activities are completed safely, accurately, and on schedule.
  • Documentation is maintained with full compliance and accuracy.
  • Cleanroom and aseptic standards are consistently followed.
  • Quality and regulatory requirements are met without deviation.
  • Strong collaboration supports efficient production and operational excellence.
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