WhatsApp Channel
Telegram Group
🧪 Analyst – Regulatory Management (Medical Devices) | Merck Life Science, India
Institution: Merck Life Science (via FYND Talent Solutions)
📍 Location: Bangalore, Karnataka, India
💼 Position Available: Analyst – Regulatory Management (Medical Devices)
🔬 Research/Functional Area: Medical Device Regulatory Affairs | Regulatory Compliance | Life Sciences | In Vitro Diagnostics (IVD)
Merck Life Science is inviting applications for the position of Analyst – Regulatory Management (Medical Devices). This opportunity is ideal for freshers and early-career professionals looking to build a career in global medical device regulatory affairs. The role involves supporting regulatory submissions, maintaining compliance documentation, and collaborating with cross-functional teams to ensure regulatory excellence across international markets.
🔬 What You’ll Work On
Support regulatory submissions for Medical Devices and IVDs across global markets.
Prepare, review, track, and maintain regulatory compliance documentation.
Assist with FDA, EU MDR/IVDR, Health Canada, and TGA regulatory submissions.
Support Technical Documentation (TD) and General Safety & Performance Requirements (GSPR) documentation.
Manage regulatory documents using Mango and Veeva Vault systems.
Collaborate with quality, regulatory, and cross-functional teams to ensure compliance.
🎓 You’re a Good Fit If
You hold a Master’s degree in Life Sciences, Biomedical Engineering, Biotechnology, or a related discipline.
You have 0–2 years of experience in Regulatory Affairs, Quality Assurance, or a related field.
You understand global medical device regulations such as FDA, EU MDR/IVDR, TGA, and Health Canada.
You are familiar with Technical Documentation, GSPR, and document management systems like Veeva Vault or Mango.
You possess excellent communication, documentation, organizational, and time-management skills.
🌟 What You’ll Gain
Work with one of the world’s leading science and technology companies.
Exposure to global Medical Device and IVD regulatory processes.
Opportunity to collaborate with experienced regulatory and quality professionals.
Hands-on experience with industry-standard regulatory documentation systems.
Excellent career growth in Medical Device Regulatory Affairs.
📝 How to Apply
Apply through the official application link:
📌 Job Details
Company: Merck Life Science
Role: Analyst – Regulatory Management (Medical Devices)
Location: Bangalore, Karnataka
Experience: 0–2 Years
Job Type: Full-Time
Job ID: 300606
📂 Category
Medical Device Regulatory Affairs | Regulatory Affairs | Life Sciences | Biomedical Engineering | Quality Assurance
🏷️ Tags
#Merck #RegulatoryAffairs #MedicalDevices #IVD #LifeSciences #BiomedicalEngineering #Biotechnology #RegulatoryJobs #BangaloreJobs #FreshersJobs #MedicalDeviceJobs #QA #CareerOpportunity
Follow Biopractify for more & Join our community : https://chat.whatsapp.com/F38FNCU0nfvFCDf1mYJDbm
About The Author
