Root Cause Investigator Specialist
Elanco, Elwood, IN, United States
Your Role: Root Cause Investigator Specialist
The Root Cause Investigator Specialist is responsible for leading and supporting root cause analysis and quality event management for monoclonal antibody production at the Elwood, Kansas site. This role partners closely with cross‑functional teams to drive thorough investigations, ensure high‑quality documentation, and implement effective corrective and preventive actions (CAPA). The position plays a key role in strengthening compliance, improving processes, and fostering a culture of quality and continuous improvement.
Your Responsibilities:
Lead and facilitate root cause investigations for quality and safety events, ensuring timely, thorough, and compliant resolution.
Collaborate with cross‑functional teams to support and mentor staff on investigation methodologies and technical writing best practices.
Author and review technical documentation including investigation reports, impact assessments, deviations, change controls, CAPAs, and standard operating procedures (SOPs).
Drive continuous improvement initiatives through data analysis, Kaizen events, and KPI‑driven discussions to enhance manufacturing performance.
Perform risk and impact assessments to support decision‑making and ensure regulatory compliance.
Ensure adherence to GMP standards and internal quality systems while promoting a strong culture of safety, quality, and accountability.
What You Need to Succeed (minimum qualifications):
Education:
Bachelor’s degree in a STEM‑related field.
Experience:
Minimum of 3 years of experience in a GMP‑regulated environment, with at least 2 years leading or supporting root cause investigations.
Top 2 Skills:
Strong root cause investigation and problem‑solving capabilities; and the ability to collaborate cross‑functionally while producing clear, high‑quality technical documentation. Strong understanding of quality systems, including deviations, CAPA, and change control processes.
What will give you a competitive edge (preferred qualifications):
Experience in commercial monoclonal antibody or recombinant protein manufacturing.
Demonstrated strength in technical writing and documentation.
Six Sigma Green Belt (or higher) or equivalent continuous improvement training.
Formal training in root cause analysis methodologies (e.g., DMAIC, 5 Whys, Fishbone).
Proven ability to collaborate across cross‑functional teams, with strong coaching and communication skills.
Additional Information:
Location: Elwood, Kansas
Travel: Occasional ( This role operates during standard business hours with occasional off‑hours support in a 24/7/365 manufacturing environment.
Elanco Benefits and Perks:
Multiple relocation packages
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
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Your Responsibilities:
Lead and facilitate root cause investigations for quality and safety events, ensuring timely, thorough, and compliant resolution.
Collaborate with cross‑functional teams to support and mentor staff on investigation methodologies and technical writing best practices.
Author and review technical documentation including investigation reports, impact assessments, deviations, change controls, CAPAs, and standard operating procedures (SOPs).
Drive continuous improvement initiatives through data analysis, Kaizen events, and KPI‑driven discussions to enhance manufacturing performance.
Perform risk and impact assessments to support decision‑making and ensure regulatory compliance.
Ensure adherence to GMP standards and internal quality systems while promoting a strong culture of safety, quality, and accountability.
What You Need to Succeed (minimum qualifications):
Education:
Bachelor’s degree in a STEM‑related field.
Experience:
Minimum of 3 years of experience in a GMP‑regulated environment, with at least 2 years leading or supporting root cause investigations.
Top 2 Skills:
Strong root cause investigation and problem‑solving capabilities; and the ability to collaborate cross‑functionally while producing clear, high‑quality technical documentation. Strong understanding of quality systems, including deviations, CAPA, and change control processes.
What will give you a competitive edge (preferred qualifications):
Experience in commercial monoclonal antibody or recombinant protein manufacturing.
Demonstrated strength in technical writing and documentation.
Six Sigma Green Belt (or higher) or equivalent continuous improvement training.
Formal training in root cause analysis methodologies (e.g., DMAIC, 5 Whys, Fishbone).
Proven ability to collaborate across cross‑functional teams, with strong coaching and communication skills.
Additional Information:
Location: Elwood, Kansas
Travel: Occasional ( This role operates during standard business hours with occasional off‑hours support in a 24/7/365 manufacturing environment.
Elanco Benefits and Perks:
Multiple relocation packages
8-week parental leave
9 Employee Resource Groups
Annual bonus offering
Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
#J-18808-Ljbffr