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Associate Director - Automation Engineering – Hybrid Manufacturing

Scorpion Therapeutics, West Lebanon, IN, United States


Role Summary The Associate Director-Automation Engineering is responsible for the supervision of the process control engineers and consultants that support the daily operations of the Hybrid facility. The role also oversees the productivity and development of the team to ensure reliable and compliant control applications and systems are used in manufacturing, and partners to influence and implement within the process control organization to support the process control technical agenda, business priorities, and compliance objectives. During the project delivery and startup phases (startup expected 2025 to 2028), leadership roles will be fluid and dynamic as the organization builds capabilities to support GMP operations and site culture.

Responsibilities

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

Set and reinforce standards for appropriate rigor in automation work products

Ensure focus by engineers and completion of critical assignments with monitoring and reporting

Foster teamwork within the department and demonstrate interpersonal skills

Maintain technical depth and rigor in deliverables

Make independent decisions and network with others as appropriate

Function as a leader and as a member of management teams

Qualifications

Required: Minimum B.S. in Engineering with experience in Automation Engineering, preferably in API and Biologics manufacturing

Required: 10+ years of experience in Biopharma engineering, operations, or manufacturing

Preferred: Experience in design, development, commissioning, and qualification of highly automated greenfield manufacturing sites utilizing SCADA, DCS, and MES systems (DeltaV, Rockwell, Syncade, etc)

Preferred: Experience as a member of group leadership in running the plant, including participation in management sub-teams

Skills

Strong leadership and people-management capabilities

Experience with process control standards, automation lifecycle, and compliance practices

Ability to drive cross-functional collaboration across automation and compliance teams

Education

B.S. in Engineering (required)

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