Senior Technical Services Scientist - External Manufacturing
Quick Summary
Champion the Continued Process Verification (CPV) program using statistical tools to ensure process robustness and preemptively mitigate manufacturing drifts.
Education: Bachelor’s Degree or advanced degree in a Life Science or Engineering field (e.g., Pharmacy, Chemistry, Chemical Engineering, or Biochemistry).
Requirements
~1 min readEducation: Bachelor’s Degree or advanced degree in a Life Science or Engineering field (e.g., Pharmacy, Chemistry, Chemical Engineering, or Biochemistry).
Experience: A minimum of 7 years of experience in Pharmaceutical/Chemical Production, Technical Science (TS/MS), Drug Development, or Quality Assurance.
Proficiency in applied statistics for data analysis and process monitoring, alongside strong technical writing and project management skills.
Experience partnering with strategic contract manufacturing organizations (CMOs).
Strong working knowledge of cGMP manufacturing environments and regulatory requirements across multiple health authorities.
Familiarity with manufacturing data stewardship systems (e.g., Veeva or similar platforms).
Advanced knowledge of pharmaceutical analytical testing and statistical software.
Proven ability to lead interdisciplinary, multicultural teams and build strong external relationships.
As a Senior Technical Services/Manufacturing Sciences (TSMS) Scientist, you will provide technical expertise and oversight for a portfolio of products produced at external contract manufacturers. In this role, you’ll be responsible for advancing the “Science, Capability, and Control” strategy to ensure technical excellence, uninterrupted supply, and successful new product launches.
Responsibilities
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Champion the Continued Process Verification (CPV) program using statistical tools to ensure process robustness and preemptively mitigate manufacturing drifts.
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Drive the technical productivity agenda at assigned contract manufacturers, focusing on manufacturing efficiency, cost improvement, and gross margin enhancement.
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Support the technical governance framework, including change management, deviation investigations, and maintaining oversight of batch processing records and quality standards.
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Lead and oversee technical transfers and new product introductions, ensuring all processes are successfully validated and meet Elanco’s manufacturing standards.
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Serve as a key technical interface for cross-functional teams and represent the TS/MS function during internal audits and external health authority inspections.
Travel: 15-25%
Location: Indianapolis, Indiana - Hybrid Work Environment
Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
What We Offer
~1 min readWe offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
Location & Eligibility
Listing Details
- Posted
- September 14, 2026
- First seen
- September 29, 2026
- Last seen
- September 29, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 23%
- Scored at
- September 29, 2026
Signal breakdown
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