Manufacturing Technician

Medivant Healthcare

Chandler (AZ)

On-site

USD 52,000 - 76,000

Full time

41 hours ago
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Job summary

Medivant Healthcare in Chandler, AZ is seeking a Cleanroom Manufacturing Technician to support sterile injectable manufacturing. You will perform aseptic production, filling, compounding, packaging, and documentation in a controlled cleanroom environment, ensuring adherence to FDA/cGMP standards and company procedures.

Responsibilities include operating equipment, maintaining cleanroom standards, and contributing to quality, safety, and continuous improvement initiatives.

Qualifications

  • Must have high school diploma or GED.
  • Ability to work in a cleanroom with required PPE.
  • Strong attention to detail and commitment to quality.
  • Ability to stand for extended periods and lift up to 25 lbs.

Responsibilities

  • Perform aseptic manufacturing, compounding, filling, and packaging activities.
  • Operate and monitor manufacturing equipment, including filling machines, autoclaves, and tanks.
  • Prepare materials and equipment for production batches.
  • Maintain cleanroom standards, gowning, and hygiene practices.
  • Complete production documentation with accuracy and compliance.

Skills

Attention to detail
Teamwork
Communication
Safety awareness
Problem solving
Documentation accuracy

Education

High school diploma or GED

Job description

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 <797>/<800> 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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