BioSpace
Associate Director – Automation Engineering Analytical Lab, System Administratio
BioSpace, Lebanon, Indiana, United States, 46052
Overview
Associate Director – Automation Engineering Analytical Lab, System Administration and Integration at Lilly (location: Indianapolis to Lebanon transition). Join to apply for the Associate Director role at BioSpace. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. Responsibilities
Supervise the process control engineers and consultants that support the daily operations of the facility. Own productivity and development of employees to ensure reliable and compliant control applications and systems in manufacturing at the Foundry. Partner to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives. During project delivery and startup phases (startup expected 2025 to 2028), provide leadership as we build a new organization, implement necessary systems and business processes for GMP operations, and shape site culture. Key Objectives / Deliverables
Administrative Leadership Supervise and coach process control team, including performance reviews and development plans Staffing, including recruiting, resource planning, and succession planning Process control work coordination Review and monitor financial performance; commit to meeting targets Develop and implement the Automation Engineering Business Plan Operational Excellence
Demonstrate a commitment to environmental, health, and safety Identify, track, and report key indicators of functional performance Ensure team operates in a state of compliance Organizational Capability
Coordinate with automation and compliance consultants to set and reinforce standards for appropriate rigor in automation work products Assure focus by engineers and completion of critical assignments with appropriate monitoring and reporting Instill teamwork within the department and demonstrate key interpersonal skills Ensure appropriate technical depth and rigor with departmental deliverables Make decisions independently and network with others as appropriate Function in a team environment as a leader and as a member of management teams Basic Requirements
B.S. in Engineering with experience in Automation Engineering, preferably in major pharmaceutical manufacturing handling Laboratory and Analytical systems and equipment, Control System Administration and Systems Integration 10+ years in Biopharma engineering, IT, operations, or manufacturing Additional Preferences
Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, MES, LIMS and Site Historian systems (DeltaV, Rockwell, Syncade, LabVantage, OSI PI) Experience in commissioning, qualifying and supporting analytical and lab equipment such as cell counters, EM, FITs Experience as a member of the group leadership in running the plant, including participation in management sub-teams Successful application of organizational models through recruiting and retention of employees Other Information
Initial location at Lilly Technology Center, Indianapolis. Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly
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Associate Director – Automation Engineering Analytical Lab, System Administration and Integration at Lilly (location: Indianapolis to Lebanon transition). Join to apply for the Associate Director role at BioSpace. At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. Responsibilities
Supervise the process control engineers and consultants that support the daily operations of the facility. Own productivity and development of employees to ensure reliable and compliant control applications and systems in manufacturing at the Foundry. Partner to influence and implement within the process control organization and across functional disciplines to support the process control technical agenda, business plan priorities, and compliance objectives. During project delivery and startup phases (startup expected 2025 to 2028), provide leadership as we build a new organization, implement necessary systems and business processes for GMP operations, and shape site culture. Key Objectives / Deliverables
Administrative Leadership Supervise and coach process control team, including performance reviews and development plans Staffing, including recruiting, resource planning, and succession planning Process control work coordination Review and monitor financial performance; commit to meeting targets Develop and implement the Automation Engineering Business Plan Operational Excellence
Demonstrate a commitment to environmental, health, and safety Identify, track, and report key indicators of functional performance Ensure team operates in a state of compliance Organizational Capability
Coordinate with automation and compliance consultants to set and reinforce standards for appropriate rigor in automation work products Assure focus by engineers and completion of critical assignments with appropriate monitoring and reporting Instill teamwork within the department and demonstrate key interpersonal skills Ensure appropriate technical depth and rigor with departmental deliverables Make decisions independently and network with others as appropriate Function in a team environment as a leader and as a member of management teams Basic Requirements
B.S. in Engineering with experience in Automation Engineering, preferably in major pharmaceutical manufacturing handling Laboratory and Analytical systems and equipment, Control System Administration and Systems Integration 10+ years in Biopharma engineering, IT, operations, or manufacturing Additional Preferences
Experience in design, development, commissioning and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, MES, LIMS and Site Historian systems (DeltaV, Rockwell, Syncade, LabVantage, OSI PI) Experience in commissioning, qualifying and supporting analytical and lab equipment such as cell counters, EM, FITs Experience as a member of the group leadership in running the plant, including participation in management sub-teams Successful application of organizational models through recruiting and retention of employees Other Information
Initial location at Lilly Technology Center, Indianapolis. Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana. Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status. #WeAreLilly
#J-18808-Ljbffr