Operations Production Specialist

Lonza; Bend (OR); On-site; Confidential; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Continuous improvement initiatives

Cross-functional collaboration

Relocation assistance

Job summary

Lonza in Bend, Oregon is hiring for a role focused on batch records and production documentation to support manufacturing readiness. This site-based position emphasizes accuracy, data integrity, and compliance within a GMP environment.

You will collaborate with Operations, Quality, and MSAT teams to drive continuous improvement and ensure audits and inspections are prepared for success. Relocation not specified, but location is Bend, Oregon.

Qualifications

• High School Diploma or GED required.
• GMP-regulated manufacturing experience in biotechnology, pharmaceutical, or medical device industries.
• Knowledge of Good Documentation Practices, data integrity principles, and electronic batch records.
• Experience supporting quality systems, investigations, or compliance activities.
• Familiarity with project management tools and continuous improvement methodologies is preferred.
• Strong communication, collaboration, and problem-solving skills.
• Ability to manage multiple priorities while maintaining attention to detail and quality standards.

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 to ensure accuracy, completeness, and data integrity.
• Support GMP compliance activities, investigations, corrective actions, and process changes.
• Help maintain inspection readiness and support internal and external 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

Quality systems

Project management tools

Continuous improvement

Communication skills

Problem solving

Education

High School Diploma or GED

Job description

United States, Bend (Oregon)

The actual location of this job is in Bend, Oregon, USA. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What You Will Get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Medical, dental, and vision insurance.
• Opportunities to lead continuous improvement initiatives.
• Exposure to cross-functional teams across Operations, Quality, and MSAT.
• The full list of our global benefits can also be found at https://www.lonza.com/careers/benefits.

What you will do

• 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 to ensure accuracy, completeness, and data integrity.
• Support GMP compliance activities, investigations, corrective actions, and process changes.
• Help maintain inspection readiness and support internal and external 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.

What we are looking for

• High School Diploma or GED required.
• Experience working in a GMP-regulated manufacturing environment, preferably within biotechnology, pharmaceutical, or medical device industries.
• Knowledge of Good Documentation Practices, data integrity principles, and electronic batch records.
• Experience supporting quality systems, investigations, or compliance activities.
• Familiarity with project management tools and continuous improvement methodologies is preferred.
• Strong communication, collaboration, and problem-solving skills.
• Ability to manage multiple priorities while maintaining attention to detail and quality standards.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Reference: R78048