GMP Ops Production Specialist - Bend, OR (Relocation)

Lonza

Bend (OR)

On-site

Confidential

Full time

5 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Competitive compensation
Agile culture
Cross-functional exposure
CI initiatives

Job summary

Lonza in Bend, Oregon, is hiring an Operations Production Specialist to help ensure safe, efficient manufacturing operations in a GMP environment. This fully site-based role requires working in close collaboration with Operations, Quality and MSAT to support production readiness and continuous improvement.

The position emphasizes real-time, in-person teamwork to achieve high quality and safety standards in medicine manufacturing.

Qualifications

  • Experience in GMP-regulated manufacturing environments.
  • Knowledge of good documentation practices and data integrity.
  • Experience supporting quality systems or investigations is a plus.
  • Strong communication and collaboration skills.
  • Ability to manage multiple priorities with attention to detail.

Responsibilities

  • Manage batch records, forms, logbooks and other controlled manufacturing documents.
  • Prepare, review and issue production documentation to support manufacturing readiness.
  • Review completed batch records and electronic data for accuracy and data integrity.
  • Support GMP compliance activities, investigations, corrective actions and process changes.
  • Help maintain inspection readiness and support audits.
  • Lead or contribute to continuous improvement and Lean manufacturing initiatives.
  • Partner with Operations, Quality and MSAT to deliver projects and improve site performance.

Skills

GMP experience
Documentation
Communication
Problem solving
Collaboration

Education

High School Diploma or GED

Tools

Electronic batch records
Project management tools

Job description

Lonza in Bend, Oregon, is hiring an Operations Production Specialist to help ensure safe, efficient manufacturing operations in a GMP environment. This fully site-based role requires working in close collaboration with Operations, Quality and MSAT to support production readiness and continuous improvement.

The position emphasizes real-time, in-person teamwork to achieve high quality and safety standards in medicine manufacturing.

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