Elanco Career Opportunity | Associate Manager Role – M Pharm – Apply
Looking to advance your career in pharmaceutical research and regulatory operations? Elanco is hiring an Associate Manager – R&D Document Management, offering a rewarding pharma R&D job for experienced M Pharm professionals. This Elanco career opportunity provides hands-on exposure to global regulatory systems, pharmacovigilance support, and document management while working with international teams in a dynamic R&D environment.
- Job Title: Associate Manager – R&D Document Management
- Location: Bangalore, India
About the Company
Elanco is a global leader in animal health, dedicated to developing innovative products and services that improve the health and well-being of farm animals and pets. An Elanco career provides opportunities to collaborate with international teams, contribute to scientific innovation, and grow in a diverse and inclusive workplace. This pharma R&D job offers exposure to global regulatory operations and advanced document management systems.
Job Description
This pharma R&D job focuses on supporting Elanco’s global regulatory and pharmacovigilance teams by managing regulatory information, reviewing data in Vault RIM, and maintaining document quality. As part of an Elanco career, the selected candidate will contribute to document migration, metadata management, publishing support, and regulatory compliance while collaborating with global stakeholders.
Key Responsibilities
- Review regulatory information entered into Vault RIM by global and affiliate teams
- Support users with Vault RIM data entry and system-related queries
- Ensure regulatory information is technically accurate within Vault RIM
- Assist publishing teams by managing export file availability
- Create and update country-specific submission templates
- Maintain accurate document metadata in Vault RIM
- Prepare and standardize PDF documents for migration
- Execute document and data migration activities
- Perform migration verification and quality reviews
- Train team members on document migration tools and processes
- Collaborate with global teams to resolve document management challenges
- Promote a positive and collaborative work environment
Eligibility Criteria
- Education: M Pharm
- Experience: 3–8 years in regulatory, document management, or related pharmaceutical functions
Required Skills
- Knowledge of Vault RIM and Vault Clinical
- Understanding of regulatory affairs and pharmacovigilance documentation
- Experience in document migration and metadata management
- Strong planning and organizational skills
- Excellent verbal and written communication skills
- Good interpersonal and relationship-building abilities
- Strong attention to detail
- Ability to work independently and within cross-functional teams
- Familiarity with quality review and compliance processes
- Flexibility to collaborate with global stakeholders
This pharma R&D job at Elanco is an excellent opportunity for professionals looking to advance in regulatory operations and document management. An Elanco career offers exposure to global pharmacovigilance systems, regulatory technologies like Vault RIM, and collaborative international projects, making it an ideal role for experienced life sciences and pharmacy professionals seeking long-term career growth.
