Associate Director Manufacturing Operation

Eli Lilly and CompanyCarolina, PR
Onsite

About The Position

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. Patients are at the center of everything we do at Lilly. We are currently hiring a Associate Director Manufacturing Operations This role supports critical work that helps bring medicines and solutions to patients responsibly and efficiently. #WeAreLilly The Associate Director-Manufacturing Operations at Lilly del Caribe, Inc. is responsible for leading and optimizing manufacturing processes, ensuring the safe, efficient, and compliant production of pharmaceutical products. This role focuses on driving continuous improvement, managing operational teams, and achieving production targets within a highly regulated environment.

Requirements

  • Bachelor's degree in engineering (Chemical, Mechanical, Industrial), Pharmacy, or a related scientific field. Master's degree preferred.
  • Minimum of 8-10 years of progressive experience in pharmaceutical manufacturing operations, with at least 3-5 years in a leadership or supervisory role.
  • In-depth knowledge of GMP regulations, FDA guidelines, and other relevant pharmaceutical industry standards.
  • Proven track record of successfully leading and developing high-performing manufacturing teams.
  • Knowledge of project management tools
  • Strong understanding of lean manufacturing principles, Six Sigma methodologies, and continuous improvement tools.
  • Excellent analytical, problem-solving, and decision-making skills.
  • Exceptional communication, interpersonal, and presentation skills, with the ability to effectively interact with all levels of the organization.
  • Demonstrated ability to manage complex projects and drive operational excellence.
  • Proficiency in enterprise resource planning (ERP) systems and manufacturing execution systems (MES).
  • Fluency in Spanish and English (written and spoken).
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Nice To Haves

  • Master's degree preferred.

Responsibilities

  • Lead and manage manufacturing operations, including production scheduling, execution, and control, to meet established targets and quality standards.
  • Oversee daily production activities, troubleshoot operational issues, and implement corrective actions to minimize downtime and maximize efficiency.
  • Develop, implement, and monitor key performance indicators (KPIs) to track operational performance and drive continuous improvement initiatives.
  • Ensure strict adherence to all Good Manufacturing Practices (GMP), regulatory requirements (FDA, EMA, etc.), and internal quality systems.
  • Manage, mentor, and develop a team of manufacturing professionals, fostering a culture of safety, quality, and operational excellence.
  • Collaborate cross-functionally with Quality Assurance, Engineering, Supply Chain, and other departments to ensure seamless operations and product delivery.
  • Identify and implement process improvements, lean manufacturing principles, and new technologies to enhance productivity, reduce costs, and improve product quality.
  • Participate in regulatory inspections and audits, providing expert support and ensuring compliance with all findings.
  • Manage departmental budget, resources, and staffing levels effectively.
  • Lead investigations into deviations and non-conformances, implementing robust root cause analysis and preventative actions.
  • Establish and sustain effective communication with various project managers and leaders to gather information regarding requirements for projects affecting the manufacturing area.
  • Define a governance framework to monitor progress and ensure achievement in accordance with approved schedules.
  • Maintain project management tools for all initiatives and provide support for related tasks, such as creating purchase orders, coordinating Gate Reviews, and other associated activities.

Benefits

  • company bonus (depending, in part, on company and individual performance)
  • company-sponsored 401(k)
  • pension
  • vacation benefits
  • eligibility for medical, dental, vision and prescription drug benefits
  • flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
  • life insurance and death benefits
  • certain time off and leave of absence benefits
  • well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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