SupportFinity™
Head of Automation Systems & Digital Integration (Director)
SupportFinity™, Hillsboro, Ohio, United States, 45133
Head of Automation Systems & Digital Integration (Director)
Genentech | Posted Sep 13, 2025 Full-time | Hillsboro, Oregon Negotiable | Master (>10 yrs) Overview
Genentech’s Hillsboro Oregon campus—Hillsboro Innovative Therapies (HIT)—serves as a critical hub for emerging cell&gene therapy manufacturing. HIT is a modern 75-acre facility just outside Portland, at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities. The Automation Systems & Digital Integration team will ensure the stability, compliance, and reliability of all automation systems essential for GMP clinical manufacturing, acting as a vital bridge between manufacturing operations and enterprise digital strategies. If you are passionate about building and leading a high-performing technical team in a dynamic environment, this is an excellent opportunity to shape the future of a brand-new facility. Responsibilities
Lead and mentor a high-performing team of engineers and technicians, fostering a culture of technical excellence and innovation. Shape and implement the long-term automation and digital integration strategy for a state-of-the-art cell and gene therapy manufacturing site. Champion digital transformation and continuous improvement by identifying and integrating emerging automation technologies to support paperless manufacturing. Drive compliant and timely system implementation and validation by partnering with QA, IT/OT, and global stakeholders. Provide subject matter expertise during internal audits and Health Authority inspections, ensuring system ownership and validation lifecycle readiness. Influence global automation strategy and best practices by representing HIT in cross-functional forums and network working groups. Oversee critical system support, including deviation investigations and performance metrics, to ensure operational continuity and data integrity for MES and other key platforms. Qualifications
Bachelor’s degree in Engineering, Computer Science, Automation, or related field; Master’s degree preferred. 12+ years of experience supporting automation systems in GMP biopharmaceutical or advanced therapy manufacturing environments. 5+ years of people leadership experience with responsibility for technical teams in a matrixed setting. Demonstrated expertise in SCADA, PLCs, BAS, and Level 1/2 automation system integration. Strong understanding of validation, GAMP principles, data integrity, and regulatory expectations for GMP systems. Proven ability to lead investigations, manage change controls, and deliver compliant system implementations. Experience partnering with IT/OT and Quality organizations to support system lifecycle activities and audit readiness. Familiarity with laboratory systems integration and analytical equipment support. Experience with Emerson DeltaV, Siemens Desigo, or similar automation platforms. Familiarity with ATMP or cell therapy-specific manufacturing processes and systems. Experience in cross-site or enterprise-wide automation governance or communities of practice. Experience representing site automation functions during regulatory inspections or industry forums. Additional Details
Relocation is approved for this posting. This is an on-site position; no remote options are offered at this time. Salary range based on Oregon location: $151,600 - $281,500. Actual pay determined by experience, qualifications, geographic location, and other factors. A discretionary annual bonus may be available. This position also qualifies for the benefits detailed in this
link . Genentech is an equal opportunity employer. It is our policy to employ, promote, and treat employees and applicants on the basis of merit, qualifications, and competence, without unlawful discrimination. If you have a disability and need an accommodation in relation to the online application process, please contact us with Accommodations for Applicants. About the company: Genentech
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Genentech | Posted Sep 13, 2025 Full-time | Hillsboro, Oregon Negotiable | Master (>10 yrs) Overview
Genentech’s Hillsboro Oregon campus—Hillsboro Innovative Therapies (HIT)—serves as a critical hub for emerging cell&gene therapy manufacturing. HIT is a modern 75-acre facility just outside Portland, at the forefront of advancing cell and gene therapy medicines through accelerated clinical and commercial manufacturing capabilities. The Automation Systems & Digital Integration team will ensure the stability, compliance, and reliability of all automation systems essential for GMP clinical manufacturing, acting as a vital bridge between manufacturing operations and enterprise digital strategies. If you are passionate about building and leading a high-performing technical team in a dynamic environment, this is an excellent opportunity to shape the future of a brand-new facility. Responsibilities
Lead and mentor a high-performing team of engineers and technicians, fostering a culture of technical excellence and innovation. Shape and implement the long-term automation and digital integration strategy for a state-of-the-art cell and gene therapy manufacturing site. Champion digital transformation and continuous improvement by identifying and integrating emerging automation technologies to support paperless manufacturing. Drive compliant and timely system implementation and validation by partnering with QA, IT/OT, and global stakeholders. Provide subject matter expertise during internal audits and Health Authority inspections, ensuring system ownership and validation lifecycle readiness. Influence global automation strategy and best practices by representing HIT in cross-functional forums and network working groups. Oversee critical system support, including deviation investigations and performance metrics, to ensure operational continuity and data integrity for MES and other key platforms. Qualifications
Bachelor’s degree in Engineering, Computer Science, Automation, or related field; Master’s degree preferred. 12+ years of experience supporting automation systems in GMP biopharmaceutical or advanced therapy manufacturing environments. 5+ years of people leadership experience with responsibility for technical teams in a matrixed setting. Demonstrated expertise in SCADA, PLCs, BAS, and Level 1/2 automation system integration. Strong understanding of validation, GAMP principles, data integrity, and regulatory expectations for GMP systems. Proven ability to lead investigations, manage change controls, and deliver compliant system implementations. Experience partnering with IT/OT and Quality organizations to support system lifecycle activities and audit readiness. Familiarity with laboratory systems integration and analytical equipment support. Experience with Emerson DeltaV, Siemens Desigo, or similar automation platforms. Familiarity with ATMP or cell therapy-specific manufacturing processes and systems. Experience in cross-site or enterprise-wide automation governance or communities of practice. Experience representing site automation functions during regulatory inspections or industry forums. Additional Details
Relocation is approved for this posting. This is an on-site position; no remote options are offered at this time. Salary range based on Oregon location: $151,600 - $281,500. Actual pay determined by experience, qualifications, geographic location, and other factors. A discretionary annual bonus may be available. This position also qualifies for the benefits detailed in this
link . Genentech is an equal opportunity employer. It is our policy to employ, promote, and treat employees and applicants on the basis of merit, qualifications, and competence, without unlawful discrimination. If you have a disability and need an accommodation in relation to the online application process, please contact us with Accommodations for Applicants. About the company: Genentech
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