Merck Hiring for Regulatory Affairs in Bangalore. Apply online for regulatory job with global exposure and growth.
Company Name: Merck
Post Name: Specialist Country Liaison – Regulatory Affairs (Operational Excellence)
Job Location: Bangalore, Karnataka
Experience Required: 1 – 5 Years
Education Qualification: Bachelor’s or Master’s degree in Pharmaceutical Sciences or equivalent
Job Type: Full-Time, Permanent
Application Mode: Online
Verified Job
Merck Hiring for Regulatory Affairs – Complete Job Details
Merck, a global leader in healthcare, life sciences, and electronics, has announced a vacancy for the position of Specialist Country Liaison – Regulatory Affairs (Operational Excellence) at its Bangalore office.
The position offers an exceptional opportunity for professionals passionate about regulatory operations, compliance management, and international collaboration. If you are looking to develop a career with one of the most respected multinational pharmaceutical organizations, this is your chance to be part of an innovative and growth-driven team.
Merck is well-known for its contribution to advancing science and technology across the globe. The company is dedicated to building a better future through innovative healthcare solutions and continuous improvement in regulatory processes. This role allows candidates to gain hands-on experience in global regulatory systems, compliance practices, and operational excellence. Merck Hiring for Regulatory Affairs
About the Role
As a Specialist Country Liaison – Regulatory Affairs, you will play a vital role in managing regulatory activities across multiple international markets. You will be responsible for coordinating post-approval submissions, renewals, and variations, ensuring compliance with health authority requirements, and maintaining up-to-date documentation in global systems. Merck Hiring for Regulatory Affairs
This role demands a blend of technical knowledge, analytical skills, and communication expertise. It is best suited for individuals who enjoy working in a cross-functional, collaborative environment while maintaining a strong focus on quality and data integrity.
The position is part of Merck’s Operational Excellence team, which focuses on process optimization, data governance, and regulatory efficiency at a global level. Merck Hiring for Regulatory Affairs
Key Responsibilities
As a Specialist Country Liaison – Regulatory Affairs, your key duties and responsibilities will include: Merck Hiring for Regulatory Affairs
- Managing Regulatory Submissions:
Coordinate and manage post-approval submissions, renewals, and CMC (Chemistry, Manufacturing, and Controls) variations to ensure timely compliance with global and regional regulatory authorities. - Documentation Readiness:
Support the preparation, review, and maintenance of regulatory documents, ensuring alignment with current standards and company policies. - Regulatory Systems Management:
Handle regulatory data and workflows through systems like Veeva Vault RIM, WebCenter, and other regulatory information management platforms. - Cross-Functional Collaboration:
Work closely with local and international teams, acting as the Single Point of Contact (SPOC) for assigned regulatory activities. - Quality and Compliance:
Maintain adherence to internal quality management systems (QMS) and ensure compliance with all applicable regulations and standard operating procedures (SOPs). - Audit and Inspection Support:
Contribute to internal and external audits by preparing necessary documentation and supporting inspection readiness initiatives. - Automation and Process Improvement:
Participate in the development and implementation of automation tools, data quality programs, and process optimization projects within the regulatory affairs function. - Training and Onboarding:
Assist in preparing training documentation for new system implementations and support onboarding activities for team members.
Required Qualifications
Educational Background
- Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or any related field.
Experience
- 1–5 years of professional experience in Regulatory Affairs, Project Management, or related areas.
- Prior experience in handling regulatory submissions and post-approval variations will be an added advantage.
Technical and Professional Skills
- Strong understanding of regulatory submission processes and QMS (Quality Management System) compliance.
- Working knowledge of Veeva Vault RIM, WebCenter, or equivalent regulatory systems.
- Good understanding of CMC documentation and regulatory procedures in pharmaceutical products.
- Excellent communication, documentation, and time management skills.
- Ability to work effectively in a fast-paced and multicultural environment.
Preferred Skills
Candidates with the following additional skills will be preferred:
- Familiarity with automation tools and data governance systems in regulatory operations.
- Experience managing international regulatory submissions and supporting process optimization initiatives.
- Exposure to artwork coordination, renewals, and product variation management.
- Strong analytical mindset with an ability to handle complex data and multiple projects simultaneously.
- Capability to coordinate efficiently between local affiliates and global regulatory teams.
About Merck
Merck is a global science and technology company committed to improving lives through healthcare, life sciences, and performance materials. Founded more than 350 years ago, Merck has become one of the most trusted names in the industry. The company’s global operations span across continents, with a strong presence in over 60 countries. Merck Hiring for Regulatory Affairs
Merck’s focus on innovation, diversity, and inclusion has made it a preferred employer for professionals across disciplines. The company fosters a culture of collaboration and integrity, where every individual is encouraged to contribute to global progress through science and technology. Merck Hiring for Regulatory Affairs
This position in Bangalore represents Merck’s commitment to building strong regulatory teams in India to support global operations. Employees will work with cutting-edge technologies and processes, ensuring compliance with regulatory standards across multiple markets. Merck Hiring for Regulatory Affairs
Why Join Merck?
Working at Merck provides exposure to world-class regulatory operations and an inclusive work culture that values learning and career growth. As part of Merck’s Regulatory Affairs team, you will gain insights into the global regulatory landscape and build a rewarding career in the pharmaceutical industry.
Benefits of Working with Merck
- Global exposure in regulatory operations and data management.
- Continuous professional growth through training and development programs.
- Opportunity to collaborate with international teams on cross-functional projects.
- A diverse, inclusive, and supportive workplace culture.
- Competitive compensation package with performance-based rewards.
- Access to advanced technology systems used globally in regulatory affairs.
Merck’s leadership invests in developing employees’ skills and creating a culture of innovation. By joining the team, you will be contributing directly to Merck’s vision of delivering life-changing products and improving health outcomes worldwide. Merck Hiring for Regulatory Affairs
Career Growth at Merck
Employees at Merck have the opportunity to grow within the organization through structured learning programs, mentorship, and exposure to international projects. The Regulatory Affairs team, in particular, plays a crucial role in ensuring product compliance and enabling successful launches in global markets. Merck Hiring for Regulatory Affairs
With Merck’s focus on operational excellence and digital transformation, this position is ideal for professionals seeking long-term growth in pharmaceutical regulatory operations.
How to Apply
Interested candidates can apply online through Merck’s official career portal. Before applying, ensure you meet all the educational and experience requirements mentioned in the job description. Merck Hiring for Regulatory Affairs
Application Process:
- Visit the official Merck careers website: https://www.merckgroup.com/en/careers.html
- Search for the position: Specialist Country Liaison – Regulatory Affairs (Operational Excellence).
- Read the complete job description and verify the eligibility criteria.
- Click on Apply Now and fill in your personal and professional details.
- Upload your updated resume and supporting documents.
- Submit the application and wait for further communication from the recruitment team.
Final Words
The Merck hiring drive for Specialist Country Liaison – Regulatory Affairs offers an exceptional opportunity for professionals who aspire to work in a globally recognized organization. The role provides exposure to international markets, regulatory systems, and innovation-driven processes. Merck Hiring for Regulatory Affairs
If you are passionate about regulatory compliance, operational excellence, and scientific advancement, this job could be the next big step in your career. Apply today and take the opportunity to become a part of Merck’s global regulatory network. Merck Hiring for Regulatory Affairs
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
