Senior Project Engineer Process Automation
Job
Genentech
Remote
$142,600 Salary, Full-Time
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Job Description
- The Position
- This role is an integral part of our Automation and Digital Engineering team, which is dedicated to delivering cutting-edge process automation solutions that bridge advanced manufacturing processes with innovative digital technologies.
- The Opportunity
- As a
- Senior Project Engineer for Process Automation Systems
- , you will be a Subject Matter Expert (SME) responsible for delivering advanced automation solutions for manufacturing, packaging, and warehouse operations.
Key duties and responsibilities include:
+ Leading the planning, design, specification, procurement, implementation, and qualification of process automation systems, including DCS, PLC/SCADA, MES, and data historian platforms. + Defining global automation architectures and system concepts, including feasibility studies and alignment with Roche engineering standards. + Managing automation system integration with process equipment, utility systems, robotics, packaging & inspection systems, and warehouse automation. + Acting as the technical and commercial interface to suppliers, integrators, engineering firms, and procurement teams, driving supplier innovation and performance. + Collaborating with multidisciplinary teams to align automation scope with project priorities and stakeholder expectations, providing regular progress updates and risk mitigation strategies. + Leading Computer System Validation (CSV), qualification activities, and commissioning efforts in compliance with GMP, FDA, EMA, and cybersecurity standards. + Supporting digital transformation initiatives through advanced process control, batch analytics, smart manufacturing, and IT/OT convergence solutions.- Who You Are
- + Bachelor's degree in Automation Engineering, Mechatronics, or a related discipline, with 5+ years of experience, preferably in the pharmaceutical or biotech industry; Master's degree is a plus + Strong background in automation architecture design, project execution, commissioning and validation + Demonstrated ability to execute complex scope on mid-sized to large-scale projects + Experience with regulatory compliance (FDA, EMA) and GMP requirements for synthetic molecule manufacturing operations + Project delivery experience in pharmaceutical manufacturing environments + Significant travel (50% or more) assignment required to meet the business need (i.
- link (http://roche.
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