Senior Manufacturing Process Optimization Analyst

Allergan

Waco (TX)

On-site

USD 90,000 - 130,000

Full time

11 days ago
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Job summary

AbbVie seeks a Production Project Manager to lead manufacturing efficiency and safety initiatives. You will coordinate cross-functional teams, monitor data inputs in SAP, LIMS, and PI, and drive continuous improvement across GMP-compliant processes.

The role emphasizes planning, execution, and documentation support. The ideal candidate has 5+ years in manufacturing, strong writing skills, and experience with tech transfer and regulatory filings.

Qualifications

  • Bachelor’s Degree or equivalent in engineering or related field.
  • At least 5 years’ experience in manufacturing/production processes.
  • Familiarity with safety, quality systems and GMP practices.
  • Proficiency in tech transfer and equipment/validation processes.
  • Strong writing skills and ability to document and communicate clearly.

Responsibilities

  • Manage production projects to improve manufacturing efficiency, safety, quality and compliance.
  • Schedule tasks and manage document reviews to meet timelines.
  • Analyze data to develop and present solutions to management.
  • Support validation activities for manufacturing equipment and troubleshoot issues.
  • Implement changes to Process Control System and ensure regulatory compliance.
  • Provide training and ensure successful rollout of new methods.
  • Maintain inventory tracking and interface with Planning for production orders and batch numbers.

Skills

Project management
Writing skills
MS Office
GMP familiarity
Tech transfer
Regulatory awareness

Education

Bachelor’s Degree or equivalent

Tools

SAP
LIMS
PI

Job description

AbbVie seeks a Production Project Manager to lead manufacturing efficiency and safety initiatives. You will coordinate cross-functional teams, monitor data inputs in SAP, LIMS, and PI, and drive continuous improvement across GMP-compliant processes.

The role emphasizes planning, execution, and documentation support. The ideal candidate has 5+ years in manufacturing, strong writing skills, and experience with tech transfer and regulatory filings.

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