Sterile GMP Packaging Operator

ROIS

Phoenix (AZ)

On-site

USD 39,000 - 48,000

Full time

30 hours ago
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Job summary

ROIS in Phoenix, AZ is seeking a Manufacturing Operator (Packaging Operator I) to support production of sterile injectable products in a regulated environment. You will follow detailed work instructions, maintain GMP/SOP compliance, and help ensure safety and quality.

The schedule is Monday-Thursday, 6:00am-4:30pm. This role requires lifting, gowning in controlled areas, accurate documentation, and teamwork with cross-functional groups to meet production goals.

Qualifications

  • High school diploma or GED required; equivalent combinations considered.
  • Experience in regulated manufacturing or GMP environment preferred.
  • Ability to read, write and understand English; basic math skills.

Responsibilities

  • Follow detailed work instructions and production procedures.
  • Prepare equipment, materials, and resources to meet schedules.
  • Operate and support sterile injectable manufacturing equipment.
  • Handle hazardous materials per regulations and policies.
  • Document production activities accurately in real time per GMP.
  • Identify and address discrepancies in procedures or documentation.
  • Participate in training and continuous improvement initiatives.
  • Collaborate with team members and cross-functional departments.

Skills

Attention to detail
Documentation accuracy
Written communication
Verbal communication
Mathematical skills
English literacy
Teamwork
Flexibility/OT
Independent work

Education

High School Diploma or GED
Equivalent education/experience

Tools

Microsoft Office
MES/HMI/Manufacturing software

Job description

ROIS in Phoenix, AZ is seeking a Manufacturing Operator (Packaging Operator I) to support production of sterile injectable products in a regulated environment. You will follow detailed work instructions, maintain GMP/SOP compliance, and help ensure safety and quality.

The schedule is Monday-Thursday, 6:00am-4:30pm. This role requires lifting, gowning in controlled areas, accurate documentation, and teamwork with cross-functional groups to meet production goals.

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