Senior Director, TS/MS – Small Molecule Manufacturing

Information Technology Senior Management Forum; Lebanon (IN); On-site; USD 168,000 - 246,000; Full time

Benefits offered by this job

401(k) plan

Pension

Medical benefits

Job summary

Lilly is seeking a Senior Director of Technical Services/Manufacturing Science (TS/MS) for Small Molecule or Peptides at the Lebanon, IN site. You will lead startup, validation, and compliance to ensure GMP manufacturing readiness and timely production of APIs, shaping the site’s technical future.

The role drives technical excellence, develops future leaders, and partners with global functions to meet corporate goals and accelerate life-changing medicines for patients worldwide.

Qualifications

• PhD in Chemistry or related field with 15+ years in pharma development and manufacturing.
• Leadership in TS/MS or similar department; large-scale manufacturing experience preferred.
• Exposure to process validation, technology transfer, and regulatory compliance.

Responsibilities

• Develop the site's strategic direction for medium and long term.
• Lead TS/MS for small molecule or peptide operations, including new product introduction and optimization.
• Develop and execute strategic and operational plans for TSMS.
• Ensure validated state of processes and regulatory compliance.
• Build partnerships with SMDD, Global TSMS, and other functions.
• Oversee preparation and timely completion of technical documentation and reports.
• Provide leadership in problem-solving, risk management, and continuous improvement.
• Coach and mentor team; manage resources and capability development.
• Represent TS/MS in governance and strategic decision-making forums.

Skills

Leadership

Strategic thinking

Regulatory compliance

Communication

Stakeholder engagement

Education

PhD in Chemistry or related field

Job description

Lilly is seeking a Senior Director of Technical Services/Manufacturing Science (TS/MS) for Small Molecule or Peptides at the Lebanon, IN site. You will lead startup, validation, and compliance to ensure GMP manufacturing readiness and timely production of APIs, shaping the site’s technical future.

The role drives technical excellence, develops future leaders, and partners with global functions to meet corporate goals and accelerate life-changing medicines for patients worldwide.