Senior Project Engineer Process Automation
AI summary of the role
This role leads the design, implementation, and qualification of process automation systems (DCS, PLC/SCADA, MES, data historians) for pharmaceutical manufacturing, packaging, and warehouse operations.
No longer in the current catalog. Last included 2026-09-09. Check the employer’s posting for availability.
What you’ll do
- Lead planning, design, specification, procurement, implementation, and qualification of process automation systems (DCS, PLC/SCADA, MES, data historian platforms).
- Define global automation architectures and system concepts, including feasibility studies and alignment with Roche engineering standards.
- Manage automation system integration with process equipment, utility systems, robotics, packaging & inspection systems, and warehouse automation.
- Act as technical and commercial interface to suppliers, integrators, engineering firms, and procurement teams.
What you’ll bring
- Bachelor’s degree in Automation Engineering, Mechatronics, or related discipline.
- 5+ years of experience, preferably in pharmaceutical or biotech industry.
- Strong background in automation architecture design, project execution, commissioning and validation.
- Experience with regulatory compliance (FDA, EMA) and GMP requirements for synthetic molecule manufacturing.
Technologies
DCS · PLC/SCADA · MES · data historian · robotics · IT/OT convergence · Computer System Validation (CSV) · GMP · FDA · EMA
About Genentech
Biotechnology company discovering and developing medicines for serious and life-threatening diseases (oncology, neuroscience, immunology); operates as Roche's independent US pharma R&D and commercial arm.
Acquired · 5000+ people
Source and classification
Internal deployment & tooling · Evidence for this classification:
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. As a member of this team, you will play a key role in designing, implementing, and managing automation systems across pharmaceutical and biotech manufacturing, packaging, and warehouse operations. You will collaborate closely with multidisciplinary stakeholders and global teams to ensure compliance, performance, and alignment with our digital transformation initiatives. This is a unique opportunity to contribute to groundbreaking projects shaping the future of pharmaceutical production. The Opportunity As a Senior Project Engineer for Process Automation Systems, you will be a Subject Matter Expert (SME) responsible for delivering advanced automation
More from the job description
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. As a member of this team, you will play a key role in designing, implementing, and managing automation systems across pharmaceutical and biotech manufacturing, packaging, and warehouse operations. You will collaborate closely with multidisciplinary stakeholders and global teams to ensure compliance, performance, and alignment with our digital transformation initiatives. This is a unique opportunity to contribute to groundbreaking projects shaping the future of pharmaceutical production. 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. You will take ownership of the entire project lifecycle, ensuring compliance, performance, and successful execution while driving progress in digital manufacturing and Industry 4.0 initiatives. 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 a [... source excerpt omitted ...] ecution, 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.e. weekly commuting and/or temporary remote assignment, including on-site presence during FAT/SAT activities, international project assignment of 1 to 3 years) The expected salary range for this position based on the primary location of Oceanside is $99,820 - $185,380. Actual pay will be dete [... source excerpt omitted ...] 2026 Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
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