Specialist – Regulatory Affairs Job at Merck Bangalore
Merck is hiring a Specialist Country Liaison – Operational Excellence, Regulatory Affairs in Bangalore! This Regulatory Affairs Job full-time role offers regulatory professionals the chance to work at the intersection of global collaboration, innovation, and compliance. If you have a background in pharmaceutical sciences and are passionate about regulatory systems, process improvement, and digital transformation, this is your opportunity to make a global impact. Graduates seeking for Pharmacy jobs or graduates who want to build their career with pharmacy careers can apply.
Introduction of the Job
Merck is seeking an experienced Specialist Country Liaison – Regulatory Affairs (Operational Excellence) to support regulatory processes across international markets. The Regulatory Affairs Job role involves managing data and documentation in regulatory systems, coordinating submissions, and ensuring compliance with global standards.
Job Details
- Position: Regulatory Affairs Job
- Location: Bangalore, Karnataka, India
- Job ID: 293034
- Employment Type: Full-time
Your Role:
- Coordinate post-approval submissions, renewals, and maintenance activities
- Manage data and documentation in regulatory systems (e.g., Veeva Vault RIM, WebCenter)
- Support preparation of Health Authority submissions
- Drive data governance, quality improvement, and automation initiatives
- Ensure compliance with global and local regulatory standards
- Serve as SPOC (Single Point of Contact) for assigned regions
- Support audit and inspection readiness activities
About the Company
Merck is a global leader in Healthcare, Life Sciences, and Electronics, committed to innovation that improves lives and advances human progress. With a diverse and inclusive culture, Merck empowers employees to explore bold ideas, drive technological transformation, and create a positive impact on patients and the planet.
Educational Requirements for Regulatory Affairs Job Role:
- University degree in Pharmaceutical Sciences or equivalent
- 1–5 years of experience in Regulatory Affairs and/or Project Management
- Experience with Veeva Vault RIM or similar regulatory platforms
- Strong analytical and documentation management skills
Key Responsibilities for Regulatory Affairs Job Role:
- Coordinate regulatory submissions and data management for multiple markets and research.
- Support artwork, labeling, and safety documentation workflows
- Assist with CMC variation preparation as per country requirements
- Maintain accurate data in global RA systems
- Contribute to process improvement and digital compliance initiatives
- Provide training support for new users and systems
- Ensure timely communication between global and local RA teams
Skills Required for Regulatory Affairs Job Role:
- Strong regulatory knowledge and understanding of submission processes
- Familiarity with Veeva Vault RIM, WebCenter, and similar platforms
- Excellent analytical, problem-solving, and communication skills
- Project coordination and multitasking ability
- Detail-oriented mindset with strong execution skills
How to Apply for Regulatory Affairs Job Role:
Interested candidates in Pharmacy jobs and want to build their career with pharmacy careers can apply through the official Merck careers portal to join a team driving regulatory excellence and global innovation.
