Manufacturing Engineer I - Biotech Operations

Amgen SA; Thousand Oaks (CA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Stock-based incentives

Flexible work models

Retirement and savings plan

Job summary

Amgen Thousand Oaks is seeking an Engineer I to support manufacturing activities related to cGMP equipment and facilities. You will collaborate with Automation, Maintenance, Project Management, and Quality Assurance to ensure equipment reliability and compliance.

The role emphasizes safety, data-driven improvements, and participation in audits, with opportunities to lead capital projects and mentor others in risk-based methods.

Qualifications

• Bachelor’s degree in engineering or related field; advanced degree preferred.
• 7+ years of relevant work experience in operations/manufacturing environments.

Responsibilities

• Lead and support engineering activities for cGMP equipment and facilities.
• Collaborate with Automation, Maintenance, and Quality Assurance to ensure equipment reliability.
• Participate in validation protocols and regulatory inspections as needed.
• Drive continuous improvement and risk-based verification on GMP equipment projects.
• Mentor project teams and provide technical guidance to engineers.

Skills

Engineering fundamentals

Manufacturing environments

cGMP compliance

Data analysis

Education

Master’s degree in engineering

Bachelor’s degree in engineering

Associate’s degree with experience

Tools

DeltaV

Rockwell

Plant Information Systems

Job description

Amgen Thousand Oaks is seeking an Engineer I to support manufacturing activities related to cGMP equipment and facilities. You will collaborate with Automation, Maintenance, Project Management, and Quality Assurance to ensure equipment reliability and compliance.

The role emphasizes safety, data-driven improvements, and participation in audits, with opportunities to lead capital projects and mentor others in risk-based methods.