Manager — R&D Quality & Compliance
Elanco View all jobs
- Bangalore, Karnataka
- Permanent
- Full-time
- Oversee and manage IAC QSC resources in alignment with R&D Quality vision and R&D priorities to deliver high-impact innovation portfolio.
- Serve as ERDQA lead for onsite R&D business functions including collaborating in a cross-matrixed environment with Clinical Operations, Data Management, Statistics, Global Operations and Transformation, Archiving, CMC Regulatory Affairs, Pharmacovigilance, and IAC site management.
- Facilitate inspection readiness, represent R&D business and ERDQA for Health Authority inspections and internal audits, including influence and defense.
- Serve as core team member for the R&D Digital Innovation Governance team. In collaboration with business and IT, develop and implement Artificial Intelligence (AI)-based strategies and solutions to advance continuous process improvement and efficiencies. Represent ERDQA for R&D AI initiatives.
- Perform Elanco Computer Systems Quality Assurance (CSQA) related activities around the update, integration, and configuration of technology to ensure compliance with relevant standards and regulations.
- Leverage metrics and expertise to drive performance and improvement.
- Develop collaborative partnerships with R&D to establish and resource Site and Global Self-Inspection and Quality Plans.
- Represent R&D Quality on Global Innovation projects as GCP (VICH GL9) and GLP (FDA, EPA, OECD or other) subject matter expert.
- Conduct GCP (VICH GL9) and GLP assessments, audits, and Quality investigations.
- Master of science in biology, chemistry, pharmacy, toxicology or similar discipline with a minimum of 10+ years relevant experience.
- 5+ years Animal Health development experience, with R&D-related Quality Assurance esp. in Quality Systems, Pharmacovigilance, Regulatory CMC and/or Data Management.
- Ability to operate in a business focused R&D Quality organization recognized as a collaborator and partner to both the R&D organization and CRO business partners.
- Knowledge in GCP (VICH GL9), GLP (FDA, EPA, OECD or other) compliance and Good Documentation Practices (ALCOA+), GPV or GMP experience a plus. Knowledge in one or more global regulatory requirements (FDA, EPA, USDA, CFIA, MHRA/VMD, EMA).
- Knowledge in regulatory requirements (e.g., Good Clinical Practice guidance (GCP, VICH Guideline 9) and / or Good Laboratory Practice (GLP) and 21 CFR Part 11 (ERES)) as related to electronic records, electronic signatures, and Good Documentation Practices (ALCOA+).
- Applicable knowledge and certifications related to Artificial Intelligence and Machine Learning or willingness to obtain.
- Familiarity with basic database design, Software Development Lifecycle, software validation, User Acceptance Testing (UAT). Elanco Animal Health Computer Systems Quality Assurance Certified preferred.
- Expert knowledge of Computer System Quality Assurance requirements.\
- Preferred qualifications
- Leads small to medium scale projects with minimum to moderate risks.
- Knowledge of business processes and the ability to work within the general business hierarchy.
- Ability to negotiate favorable outcomes while maintaining positive working relationships.
- Aware of risk-assessment methodologies, and project organization.
- Able to interpret regulations and policies, and to communicate and respond to associated questions.
- Ability to define problems, collect and review data, establish facts and draw valid conclusions.
- Ability to effectively communicate verbally and in writing.
- Ability to effectively work with teams.
- Ability to set priorities and manage multiple tasks.
- Travel: 0%
- Location: IN, Bangalore - Hybrid Work Environment
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