GMP Operations Specialist – Bend, OR

Socket.dev; Bend (OR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Job summary

Lonza in Bend, Oregon, is hiring an Operations Production Specialist to help run manufacturing operations safely and in GMP compliance. This fully site-based role collaborates with Operations, Quality, and MSAT to support production readiness and process improvements.

You will manage batch records, prepare documentation, ensure data integrity, assist audits, and contribute to continuous improvement initiatives. Relocation is available for eligible candidates.

Qualifications

• Diploma or GED required.
• GMP-regulated manufacturing experience preferred.
• Knowledge of Good Documentation Practices and data integrity concepts.
• Experience with quality systems, investigations, or compliance activities.
• Familiarity with continuous improvement methodologies is a plus.
• Strong communication and collaboration skills; ability to manage multiple priorities.

Responsibilities

• Manage batch records, forms, logbooks, and other controlled manufacturing documents.
• Prepare, review, and issue production documentation to support manufacturing readiness.
• Review 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 teams to deliver projects and improve site performance.

Skills

GMP experience

Documentation practices

Data integrity

Electronic batch records

Project management tools

Continuous improvement

Communication skills

Team collaboration

Attention to detail

Education

High School Diploma or GED

Job description

Lonza in Bend, Oregon, is hiring an Operations Production Specialist to help run manufacturing operations safely and in GMP compliance. This fully site-based role collaborates with Operations, Quality, and MSAT to support production readiness and process improvements.

You will manage batch records, prepare documentation, ensure data integrity, assist audits, and contribute to continuous improvement initiatives. Relocation is available for eligible candidates.