Director, Analytical Development β SMTD
Elanco
August 11, 2026
Remote friendly (Indianapolis, IN)
United States
Operations
Director, Analytical Development
Responsibilities:
- Guide, coach, and develop a high-performing team of 5β10 scientists.
- Provide scientific and operational direction for analytical development projects from early-stage through technical transfer to manufacturing.
- Develop and implement analytical strategies for the team/portfolio aligned with departmental and SMTD objectives.
- Serve as a key subject matter expert for complex analytical challenges; provide technical guidance and represent Elanco in regulatory interactions.
- Foster cross-functional alignment with R&D, Manufacturing, Regulatory, and external partners.
Qualifications:
- Education: PhD in Analytical Chemistry/Pharmaceutical Sciences (or related) OR Masterβs with extensive equivalent experience.
- Experience: 8+ years (PhD) or 12+ years (Masterβs) progressive pharmaceutical industry experience in analytical and CMC development for drug products.
- Skills: Deep small-molecule analytical development expertise; drug product performance testing knowledge (e.g., dissolution); strong understanding of global regulatory expectations (GMP, VICH); proven ability mentoring scientific teams.
Preferred Qualifications:
- Experience in animal health pharmaceuticals.
- Track record overseeing technology transfer to manufacturing sites.
- Experience managing CRO/external partnerships.
- Advanced analytical techniques (e.g., HPLC, HILIC, SEC, MS, NIR).
- Strategic planning and organizational leadership; influence global cross-functional outcomes.
Additional Information:
- Travel: 5β10% international. Location: Indianapolis, IN (Hybrid).
Benefits (highlights):
- Multiple relocation packages; two weeklong shutdowns; 8-week parental leave; annual bonus; flexible work arrangements; up to 6% 401(k) matching.
Application Instructions:
- Applications accepted on an ongoing basis.
Responsibilities:
- Guide, coach, and develop a high-performing team of 5β10 scientists.
- Provide scientific and operational direction for analytical development projects from early-stage through technical transfer to manufacturing.
- Develop and implement analytical strategies for the team/portfolio aligned with departmental and SMTD objectives.
- Serve as a key subject matter expert for complex analytical challenges; provide technical guidance and represent Elanco in regulatory interactions.
- Foster cross-functional alignment with R&D, Manufacturing, Regulatory, and external partners.
Qualifications:
- Education: PhD in Analytical Chemistry/Pharmaceutical Sciences (or related) OR Masterβs with extensive equivalent experience.
- Experience: 8+ years (PhD) or 12+ years (Masterβs) progressive pharmaceutical industry experience in analytical and CMC development for drug products.
- Skills: Deep small-molecule analytical development expertise; drug product performance testing knowledge (e.g., dissolution); strong understanding of global regulatory expectations (GMP, VICH); proven ability mentoring scientific teams.
Preferred Qualifications:
- Experience in animal health pharmaceuticals.
- Track record overseeing technology transfer to manufacturing sites.
- Experience managing CRO/external partnerships.
- Advanced analytical techniques (e.g., HPLC, HILIC, SEC, MS, NIR).
- Strategic planning and organizational leadership; influence global cross-functional outcomes.
Additional Information:
- Travel: 5β10% international. Location: Indianapolis, IN (Hybrid).
Benefits (highlights):
- Multiple relocation packages; two weeklong shutdowns; 8-week parental leave; annual bonus; flexible work arrangements; up to 6% 401(k) matching.
Application Instructions:
- Applications accepted on an ongoing basis.