Senior TS/MS Associate: CPV, Tech Transfers, Hybrid

Indiana Ag Connection; Indianapolis (IN); Hybrid; USD 110,000 - 150,000; Full time

Benefits offered by this job

Relocation packages

Annual bonus offering

Flexible work arrangements

8-week parental leave

Up to 6% 401K matching

Job summary

Elanco in Indianapolis, IN is seeking a Senior Technical Services/Manufacturing Sciences Associate to provide technical oversight for products produced at external contract manufacturers. You will drive CPV programs, ensure process robustness, and support transfers and new product introductions.

The role requires 7+ years in pharma/chemical production, proficiency in statistics, strong writing and PM skills, and experience with cGMP and audits. Travel 15-25% and a hybrid work environment.

Qualifications

• Bachelor's degree in Life Science or Engineering or advanced degree.
• 7+ years in Pharmaceutical/Chemical Production, TS/MS, Drug Development, or QA.
• Proficiency in applied statistics for data analysis and process monitoring, strong writing and PM skills.

Responsibilities

• Champion CPV program using statistical tools to ensure process robustness.
• Drive technical productivity and cost improvements at CMOs.
• Support governance: change management, deviations, batch records, quality standards.
• Lead technical transfers and new product introductions with GMP compliance.
• Represent TS/MS in audits and health authority inspections.

Skills

Statistics

Project management

Technical writing

Education

Bachelor's degree in Life Science or Engineering

Tools

Veeva

Statistical software

Job description

Elanco in Indianapolis, IN is seeking a Senior Technical Services/Manufacturing Sciences Associate to provide technical oversight for products produced at external contract manufacturers. You will drive CPV programs, ensure process robustness, and support transfers and new product introductions.

The role requires 7+ years in pharma/chemical production, proficiency in statistics, strong writing and PM skills, and experience with cGMP and audits. Travel 15-25% and a hybrid work environment.