Sr Engineer I, Automation (Syncade MES)
- Compensation
- $93K–$121K / yr
- Location
- Research Triangle Park, NC
- Work setup
- Not specified
- Seniority
- Senior
- Employment
- Not specified
- Experience
- Not specified
- Category
- Not specified
- Posted
Skills
Must have
- Bachelor’s degree in Engineering
- 5–8+ years of automation engineering experience in a regulated environment (GMP preferred)
- Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process support
- Strong understanding of GxP compliance, data integrity, and change control processes
- Proven ability to independently troubleshoot and resolve complex technical issues
Nice to have
- Experience with Emerson DeltaV (DCS) integration and support
- Experience with AVEVA PI System for data collection and analytics
- Familiarity with Infobatch for batch reporting
- Participation in system upgrades, tech transfers, or manufacturing modernization initiatives
Full description
About This Role
We are seeking an experienced technical contributor to join our Automation Systems Engineering team at the Biogen RTP Bio site. The Senior Automation Engineer I will support Syncade (MES) system administration within a GMP-regulated manufacturing environment. This role operates with a high degree of independence and is accountable for ensuring system reliability, supporting manufacturing execution, and driving continuous improvement initiatives. The Senior Automation Engineer I will be a subject matter expert for Syncade, capable of leading small-to-moderate complexity initiatives to influence cross-functional outcomes.
What You’ll Do
- Act as system administrator/SME for Syncade (MES), including configuration, maintenance, troubleshooting, and lifecycle management
- Own and support Syncade Application and the relevant infrastructure to enable electronic batch record (eBR) workflows, recipe configuration, and exception handling
- Ensure system availability, performance, and data integrity to support GMP manufacturing operations
- Lead root cause investigations and implement corrective/preventive actions for MES-related deviations
- Manage user access, security roles, and audit trail reviews in compliance with GxP and cybersecurity requirements
- Execute and support change controls, including system updates, enhancements, and validation deliverables (IQ/OQ/PQ)
- Drive continuous improvement efforts to enhance system usability, reliability, and operational efficiency
- Support integration and data flow between Syncade and other automation and Enterprise systems, e.g. DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMS
- Provide technical support during manufacturing operations, including off-hours support as required
Who You Are
You are a meticulous professional with a strong foundation in automation / manufacturing systems engineering, particularly in biopharmaceutical settings. Your analytical mindset and problem-solving skills empower you to tackle complex challenges independently. You thrive in collaborative environments, easily engaging with diverse teams to achieve shared goals. Your
dedication to operational excellence and compliance ensures that systems run smoothly and efficiently.
Required Skills
- Bachelor’s degree in Engineering
- 5–8+ years of automation engineering experience in a regulated environment (GMP preferred)
- Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process support
- Strong understanding of GxP compliance, data integrity, and change control processes