Engineer I
Amgen · Thousand Oaks, CA
OtherFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Amgen seeks an Engineer I to support manufacturing operations for cGMP equipment and facilities at its Thousand Oaks site. The role involves equipment reliability, capital project oversight, validation documentation, and continuous improvement while ensuring safety and quality compliance across biotech production.
What they're looking for
- Master's degree, or Bachelor's degree with 2+ years engineering/manufacturing experience
- Bachelor's degree in engineering or science-related field (preferred)
- 7+ years relevant experience with 5+ years in operations/manufacturing environment (preferred)
- Direct experience with regulated environments (FDA, OSHA, EPA)
- Knowledge of cGMP procedures and pharmaceutical/biotech production processes
- Experience with risk-based verification, validation protocols, and GMP equipment automation
- Strong technical writing and communication skills
What you'll be doing
- Support manufacturing activities and drive equipment performance, reliability, safety, and quality compliance
- Lead capital projects and provide data to support business cases and long-term strategy
- Develop design modifications to address risks and ensure validation protocols are executed per cGMP standards
- Act as liaison between Engineering, Automation, Maintenance, and Quality Assurance during project planning and execution
- Lead continuous improvement initiatives and multidisciplinary teams to reduce cost and improve safety and quality
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.