Pharma Packaging Specialist - Finishing Line

AbbVie Inc.

Waco (TX)

On-site

USD 25,000 - 39,000

Full time

6 days ago
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Job summary

AbbVie Inc. is seeking a Production Specialist I for the UD Packaging line on a 7am-7:30pm schedule (Thu-Sat, and every other Wednesday). You will support setup, changeover, and packaging of pharmaceutical products while maintaining safety and quality as top priorities.

You will contribute to a team environment, perform line clearances, operate automated equipment, and execute quality checks throughout the production run. This role requires stamina and a strong commitment to cGMP standards.

Qualifications

  • High school education or equivalent; technical certificate preferred.
  • Commitment to quality and regulatory compliance.
  • Ability to communicate issues to engineering and mechanical teams.
  • Basic computer skills and willingness to learn new programs.
  • Understanding of cGMP requirements is preferred.

Responsibilities

  • Adhere to safety procedures and promote a proactive safety culture.
  • Perform housekeeping on finishing lines and line clearances for changes.
  • Assist in setup of automated equipment in packaging areas.
  • Operate automated and semi-automated equipment to produce finished product.
  • Perform in-process checks, sample pulls, and quality-related tasks.
  • Sustain 6S of parts and tooling on the production floor.
  • Escalate safety, quality and technical issues promptly.
  • Communicate improvement opportunities with cross functional teams.
  • Troubleshoot minor equipment issues and adjust for efficiency.

Skills

Safety awareness
Team collaboration
Problem solving
Basic computer skills

Education

High school education or equivalent

Tools

SAP
MAXIMO
POMs

Job description

AbbVie Inc. is seeking a Production Specialist I for the UD Packaging line on a 7am-7:30pm schedule (Thu-Sat, and every other Wednesday). You will support setup, changeover, and packaging of pharmaceutical products while maintaining safety and quality as top priorities.

You will contribute to a team environment, perform line clearances, operate automated equipment, and execute quality checks throughout the production run. This role requires stamina and a strong commitment to cGMP standards.

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