Sr Director - Tech at Lilly Manufacturing & Quality
Scorpion Therapeutics, Houston, Texas, United States, 77246
Role Summary
Sr Director - Tech at Lilly Manufacturing & Quality will spearhead the IT landscape for a new site, reporting to the M&Q IT VP and the Manufacturing Site Head. The role shapes the Digital agenda and transformation for the facilities, building and operating a high-tech, integrated manufacturing environment. Responsibilities
Ensure site operational readiness from IT perspective, including site start up and integration of IT systems such as infrastructure, warehouse management & logistics, data historian, real-time floor tracking, digital plant, laboratory information management, CAPA, access security, building monitoring, risk management, and MES. Member of the Site Leadership Team and provide IT site functional leadership. Develop and implement site IT strategic and business plan; benchmark innovative solutions; adapt road map to site evolution and trends; partner cross-functionally locally and globally to establish site IT roadmap; maintain a safe work environment. Staffing to meet the site and functional agenda; lead, coach, and develop team members; establish a site culture aligned with Lilly values and operational excellence; lead recognition, pay, promotions; talent assessment and succession planning; support site recruiting to build IT capability. Ensure IT organization is functionally strong and operationally centered; maintain a solution-focused organization; prioritize work and remove barriers; oversee technical activities; promote knowledge sharing and education. Qualifications
Required: A Bachelor’s Degree in IT, Computer Science, Engineering, or related technical field. Required: 10+ years of leadership in Pharma IT with a focus on manufacturing IT/OT leadership experience. Preferred: 10+ years of experience with MES system implementations, data integration and advanced analytics. Preferred: Flexibility to localize in any part of the US; ability to travel to US and global Lilly sites as required, up to 50% of the time. Skills
Deep knowledge of regulatory compliance (cGMP). Proven leadership and team-building excellence. Agile management of multiple projects with adaptability to shifting priorities. Collaborative spirit with cross-functional teams. Exceptional written and verbal communication skills. Creative and analytical mindset to resolve complex issues. Deep technical knowledge of pharmaceutical manufacturing and IT/OT footprint to support the site. Creative thinking, analytical thinking, and strong problem-solving abilities. Education
Bachelor’s Degree in IT, Computer Science, Engineering, or related technical field 10+ years of leadership in Pharma IT with a focus on manufacturing IT/OT Additional Requirements
Role is on-site, Monday through Friday; must be flexible to support production schedules, shutdowns, and occasional extended hours. Position based at one of Lilly’s new API manufacturing sites in the US (Houston, TX or Virginia) with travel to other sites as required.
#J-18808-Ljbffr
Sr Director - Tech at Lilly Manufacturing & Quality will spearhead the IT landscape for a new site, reporting to the M&Q IT VP and the Manufacturing Site Head. The role shapes the Digital agenda and transformation for the facilities, building and operating a high-tech, integrated manufacturing environment. Responsibilities
Ensure site operational readiness from IT perspective, including site start up and integration of IT systems such as infrastructure, warehouse management & logistics, data historian, real-time floor tracking, digital plant, laboratory information management, CAPA, access security, building monitoring, risk management, and MES. Member of the Site Leadership Team and provide IT site functional leadership. Develop and implement site IT strategic and business plan; benchmark innovative solutions; adapt road map to site evolution and trends; partner cross-functionally locally and globally to establish site IT roadmap; maintain a safe work environment. Staffing to meet the site and functional agenda; lead, coach, and develop team members; establish a site culture aligned with Lilly values and operational excellence; lead recognition, pay, promotions; talent assessment and succession planning; support site recruiting to build IT capability. Ensure IT organization is functionally strong and operationally centered; maintain a solution-focused organization; prioritize work and remove barriers; oversee technical activities; promote knowledge sharing and education. Qualifications
Required: A Bachelor’s Degree in IT, Computer Science, Engineering, or related technical field. Required: 10+ years of leadership in Pharma IT with a focus on manufacturing IT/OT leadership experience. Preferred: 10+ years of experience with MES system implementations, data integration and advanced analytics. Preferred: Flexibility to localize in any part of the US; ability to travel to US and global Lilly sites as required, up to 50% of the time. Skills
Deep knowledge of regulatory compliance (cGMP). Proven leadership and team-building excellence. Agile management of multiple projects with adaptability to shifting priorities. Collaborative spirit with cross-functional teams. Exceptional written and verbal communication skills. Creative and analytical mindset to resolve complex issues. Deep technical knowledge of pharmaceutical manufacturing and IT/OT footprint to support the site. Creative thinking, analytical thinking, and strong problem-solving abilities. Education
Bachelor’s Degree in IT, Computer Science, Engineering, or related technical field 10+ years of leadership in Pharma IT with a focus on manufacturing IT/OT Additional Requirements
Role is on-site, Monday through Friday; must be flexible to support production schedules, shutdowns, and occasional extended hours. Position based at one of Lilly’s new API manufacturing sites in the US (Houston, TX or Virginia) with travel to other sites as required.
#J-18808-Ljbffr