Primary Skills: Root Cause Analysis (advanced), Biopharmaceutical/Process Equipment (advanced), Process Improvement (advanced), Equipment Qualification (advanced), GMP Compliance (advanced), Root Cause Analysis/RCA (intermediate), Statistical Process Control/SPC (intermediate), Maintenance (intermediate), Equipment Troubleshooting (intermediate)
Contract Type: W2 Contract
Duration: 12+ Months
Location: Thousand Oaks, CA (Fully Onsite)
Pay Range: $38.00 - $43.00 Per Hour
Job Summary:This role focuses on ensuring the reliable operation of clinical and commercial facilities and equipment within a biopharmaceutical manufacturing environment. The engineer will be instrumental in integrating new technologies and driving engineering-based improvements to existing systems. Key responsibilities include system ownership, troubleshooting, and supporting new product introductions to minimize production downtime.
Key Responsibilities:
- Own and maintain biopharmaceutical process equipment systems.
- Lead and implement engineering improvements and upgrades for equipment and facilities.
- Coordinate maintenance to maximize system performance and uptime.
- Oversee commissioning and qualification of systems, interacting with inspectors.
- Diagnose and resolve issues to reduce production downtime and implement corrective actions.
Must-Have Skills:
- Ability to analyze problems and propose data-driven engineering solutions.
- Strong technical troubleshooting skills with P&IDs and electrical drawings.
- Effective collaboration with diverse teams and adaptable support.
Domain / Industry Experience: Experience in biopharmaceutical operations and manufacturing within a regulated environment, including familiarity with GMP quality systems, is highly preferred.
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