Senior Associate-Clinical Operations

FR01 Elanco France SAS

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IN - Bangalore Until 8/22/2026 2+ years exp H-1B sponsor history First posted June 8, 2026 Last posted June 8, 2026
Job description

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

Job Opportunity: Specialist, Global Procedures and Training

Position Type: Full Time

Location: Bengaluru, India

Position Description:

The Specialist, R&D Quality Systems & Global Training, is responsible for the independent execution and support of Elanco’s R&D quality and training framework. This role requires a professional who can apply a solid understanding of Quality Management Systems (QMS) to ensure global compliance.

As a contributor, you are expected to be a high-executor who manages day-to-day activities with minimal oversight, utilizing strong judgment-based skills to prioritize tasks effectively. You will leverage technology enhanced tools to drive productivity, visualize compliance data. Maintain seamless document control within the Veeva Quality Vault and SuccessFactors. This position is ideal for an individual who can independently connect with global stakeholders to ensure R&D deliverables meet regulatory expectations.

Function Duties and Tasks:

QMS Operations: Independently manage R&D quality management system tasks, including metrics collection, document tracking, and status reporting.

Training Delivery: Execute the Global Quality System for R&D, ensuring the "right training, right employee, right timing" to maintain global compliance.

AI & Data Productivity: Apply AI-based solutions alongside Power BI to identify trends, visualize compliance gaps, and streamline the reporting process for R&D management.

Documentation & Job Aides: Author and maintain job aides and working documents that detail operational procedures with high technical accuracy.

System Proficiency: Serve as a key user and administrator for R&D support systems, including Veeva Quality Vault, SuccessFactors, MS Word, and Adobe Acrobat.

Compliance Support: Support compliance audits and regulatory inspections by providing organized, accurate documentation and data-driven process insights.

Ad-hoc Metrics Assistance: Assist with the update of Power BI metrics and reporting tools when necessary to support the communication of compliance status.

 

Key Leadership Responsibilities:

Cross-Functional Coordination: Proactively connect and interact with stakeholders across R&D, Regulatory, and Quality functions to align on deliverables.

Independent Problem Solving: Identify procedural issues and proactively search for solutions, escalating complex matters only when necessary.

Collaboration: Work effectively within and across Elanco R&D teams and external partners to achieve team objectives.

Operational Excellence: Deliver individual objectives in a high-quality, timely, and cost-effective manner, demonstrating a "Play to Win" mentality.

Adaptability: Demonstrate learning agility and flexibility when navigating changing priorities or new system implementations.

Culture: Contribute to a positive, engaging work environment aligned with Elanco’s core values and objectives.

Minimum Qualification (Education, Experience, and/or Training):

Education: Bachelor’s degree in a scientific, business, or related field.

Experience: 2+ years of relevant experience in document management, quality systems, or regulated environments (1-2 years for high-potential candidates).

Judgment: Demonstrated ability to exercise sound professional judgment and work independently with minimal daily oversight.

QMS Knowledge: Thorough understanding of Quality Management Systems and the importance of regulatory compliance in R&D.

Communication: Strong written and verbal communication skills; ability to interact professionally with global partners across different time zones.

Execution: Proven ability to prioritize a diverse workload and meet strict timelines under pressure.

Additional Preferences:

Data Analytics: Proficiency in Power BI for creating dashboards and visualizing complex data sets.

AI Literacy: Exposure to practical use of AI/Persona to enhance work efficiency and data visualization.

Technical Systems: Advanced proficiency in Veeva Vault or similar electronic document management systems (EDMS).

LMS Knowledge: Experience working with Learning Management Systems such as SuccessFactors.

 Other Information:

Travel: Limited travel required (≤5%).

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

Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

About this role

Summary

Manage quality systems, support compliance, and coordinate training in R&D environment.

Job title

Senior Associate-Clinical Operations

Experience level

2+ years

Minimum experience

2+ years exp

Industry

pharmaceuticals

Location requirements

Bangalore, India; limited remote work allowed

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

document managementquality systemsregulatory compliancePower BIVeeva VaultSuccessFactors

Preferred skills

Power BIAIVeeva VaultSuccessFactors

Specializations

quality management systemsdocument managementregulatory compliancedata visualizationAI
Locations

Structured locations inferred from the posting.

Bengaluru, Karnataka, India

On-site City
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