Role OverviewJoin Amgen's Mission of Serving Patients. As a Senior Manufacturing Systems Engineer, you will provide automation technical leadership to a group of automation engineers who are responsible for building and maintaining various automation systems and platforms that support the GMP Drug Substance Plant Operations.
What You Will Do
Develop and maintain the process control system on Emerson DeltaV distributed control system (DCS). Work with process subject matter experts (SMEs) to understand key process requirements and transform them into digital automated solutions. Collaborate with business partners to understand how automation can improve workflow and productivity.
Why It Might Be a Fit
The ideal individual must be a self-directed team player ready to mentor and develop engineering staff and embrace a team-based culture that relies on collaboration for effective decision-making. Strong leadership, technical writing, and communication/presentation skills are required.
Requirements
- High School Diploma / GED and 10 years of Engineering experience
- Associate’s Degree and 8 years of Engineering experience
- Bachelor’s Degree and 4 years of Engineering experience
- Master’s Degree and 2 years of Engineering experience
- Doctorate Degree
- Degree in Electrical Engineering, Computer Science, Chemical Engineering, Biotech Engineering, or related field
- Direct knowledge of Automation System design, experience in process control engineering and troubleshooting with GMP biopharmaceutical production facility equipment/systems automation
- Extensive understanding and background in programming, design, installation and lifecycle management of manufacturing process controls, automation and field instrumentation technologies
- Experience with Emerson DeltaV DCS system, Process Control Network design including network segregation, virtual infrastructure design and implementation, and ability to perform sophisticated troubleshooting activities, system integration using OPC, Foundation Fieldbus, Profibus, and DeviceNet technologies
- Ability to interpret and apply GAMPs and GMPs and familiarity with documentation in a highly regulated environment with requirements such as 21 CFR Part 11, ASTM 2500, S88, and S95
- Experience in Capital Project Lifecycle Management: Conceptual Design, Scope and cost estimate development, business case development, detailed design, engineering and validation documentation and project execution
- Demonstrated hands-on experience in developing process control strategies for New Product Introduction and New Technology Deployment for Drug Substance Plant Operations
- Demonstrated experience with continuous improvements resulting in enhanced safety, system reliability, and productivity (e.g. cycle times, and reduced plant utilities usage etc.) related to Drug Substance Plant Operations
Benefits
- Competitive and comprehensive Total Rewards Plans
- Base salary
- Inclusive environment of diverse, ethical, committed and highly accomplished people
- Collaborative culture
- Reasonable accommodation for individuals with disabilities
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