Associate Director - Radioligand Therapies Operations

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.

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 35,000 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.

The Associate Director / Director in Indy RLT Operations is responsible for overseeing the day - to - day activities of their operational area as well as planning for the 3-to-6-month horizon.  They are expected to lead by example and provide coaching to others in the areas of safety, quality, manufacturing operations, and continuous improvement.  The Associate Director / Director is also responsible for leading their respective process team per Manufacturing Standard for Operational Excellence (MSOE) 602.

Key Objectives / Deliverables:

• Responsible for maintaining a safe work environment, leading safety initiatives, and working safely and accountable for supporting all HSE Corporate and Site Goals.
• Responsible for a work force of approximately 25-30 individuals on various shifts.
• Train and develop reports and area supervisors through the PM process as well as education of operators on the technical aspects of product manufacturing / packaging.
• Ensure consistency of operations across shifts through active engagement on the shop floor and through Practice vs. Procedure.
• Provide leadership and develop objectives to deliver the business plan as it relates to production, financial, safety, quality, stewardship, and people.
• Maintain metrics to measure performance against business objectives and make necessary changes to improve performance.
• Participate in the development and implementation of strategies associated with the area and sponsor and support C4I, CAPA / RCA, FMEA, and Lean 6 Sigma utilization or implementation within the area.
• Function as a primary contact for other areas such as Planning, HR, TS/MS, Quality Assurance, Engineering and Environmental / Safety issues.
• This role has direct interaction with Regulatory Agencies during Site Inspections.
• Responsible for Leading Operations Process Team, a cross functional group charged with making medicine, continuous improvement, and site support.
• Understand and influence the manufacturing control strategy for their area.
• Represent their process team on the plant flow team.
• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

Minimum Requirements:

• Bachelors’ Degree in relevant industry (STEM degree preferred)
• 3+ years of experience in cGMP operations
• 1+ year of previous experience in cGMP operations leadership

Additional Preferences:

• Six Sigma Green Belt or Black Belt certification
• Previous demonstration of strong leadership skills
• Strong interpersonal and communication skills
• Understanding of Statistical Process Control and 6 Sigma concepts
• Solid understanding of quality and corporate policies
• Solid understanding of the importance of and basic requirements of Regulatory agencies such as the FDA, EMEA, OSHA and EPA
• Comprehension of MSOEs
• Demonstrated solid judgment and initiative
• Enthusiastic, positive attitude, and flexible
• Previous experience in operations or directly supporting operations (practical operational knowledge)

Additional Information:

• Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, respirator, etc.)
• Some travel may be required (<5%)
• This role is within a facility that handles radioisotopes.

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