Senior Director of Analytical Development - SMDD

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Indianapolis, IN, USA
In-Office
152K-222K Annually
Healthtech • Biotech • Pharmaceutical
The Role

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.

For more than 140 years, Lilly has been dedicated to discovering and developing medicines to make lives better for people around the world. The Product Research and Development (PRD) organization, within Lilly Research Labs is focused on discovery and development of new medicines across a range of different modalities.  Within PRD, Synthetic Molecule Design and Development (SMDD) is an innovation-focused organization striving to identify, develop, and apply transformative technologies to deliver maximum benefit to our patients. We apply our expertise across the entire lifecycle of an asset ranging from the discovery/development interface through regulatory submission and post-approval changes. We work to improve patient outcomes by delivering safe, scalable, sustainable, and reliable products and processes across a diverse portfolio of synthetic assets including small molecules, peptides, and oligonucleotides. The technical and business solutions that we develop accelerate the delivery of medicines to patients and allow the company to reinvest in the next generation of life-saving therapeutics.

We are seeking a Sr. Director of Analytical Development to provide leadership and delivery of the SMDD portfolio, with a vision of building a world-class, analytical sciences team.  This role will report to the Associate Vice President of Analytical and Tides Development and will be responsible for delivering an ambitious portfolio across different modalities, therapeutic areas, and drug substance / drug product.   

Key Responsibilities

People and Team Management

  • Build a high-performance analytical team culture that operates with clarity of roles, responsibilities, and expectations for both individuals and the team.
  • Actively manage internal and external resources to drive analytical development across the portfolio
  • Ensure safety of employees and facilities through implementation of robust safety programs / procedures.
  • Recruit, develop and grow the next generation of analytical leaders.

Portfolio Delivery and Analytical Strategy

  • Provide strategic guidance to analytical, synthetic, and formulation teams including integration and application of new technologies.
  • Partner with cross-functional teams including Quality, Regulatory, and manufacturing to ensure seamless integration of analytical development activities.
  • Identify opportunities for continual improvement projects that optimize business processes related to analytical development.
  • Possess deep understanding of the portfolio, project objectives, and how the technical programs and teams are poised to deliver on those objectives.
  • Communicate and support execution of SMDD’s technical and analytical strategy.
  • Evaluate the analytical organization’s strengths and needs and drive appropriate changes.
Basic Qualifications:
  • PhD in Organic Chemistry, Analytical Chemistry, or related field with 10+ years of experience in analytical development and commercialization of drug substances and drug product  (Will also consider a MS Degree in Organic Chemistry, Analytical Chemistry, or related field with 12+ years of experience OR a BS Degree in Organic Chemistry, Analytical Chemistry, or related field with 15+ years of experience)
Additional Skills / Preferences:
  • 10+ years of CMC analytical experience
  • Previous supervisory and management experience
  • Excellent communication (written and verbal)
  • Outstanding teamwork/Interpersonal/Leadership/Vision
  • External network and networking skills
  • Expertise in project planning/organization/management
  • Talent assessment and recruiting
  • Direct experience in early to late phase analytical development, product characterization, and commercialization of synthetic molecule products

Additional Information: 

  • Travel: 0 to 10% 
  • Position Location: Local/Onsite in Indianapolis, IN.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location.  The anticipated wage for this position is

$151,500 - $222,200

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a 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; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

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The Company
HQ: Indianapolis, IN
39,451 Employees
Year Founded: 1876

What We Do

Eli Lilly and Company engages in the discovery, development, manufacture, and sale of products in pharmaceutical products business segment. For more than a century, we have stayed true to a core set of values – excellence, integrity, and respect for people – that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities through philanthropy and volunteerism.

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