Regulatory Affairs Intern

🚀 We're Hiring: Regulatory Affairs Intern / Trainee (IVD Industry)
📍 Location: Charkop, Kandivali (West), Mumbai

Are you a recent graduate passionate about Regulatory Affairs, Medical Devices, and the IVD industry? This is a great opportunity to kick-start your career and gain hands-on experience in regulatory compliance, product registrations, and medical device documentation.

Eligibility
🎓 Bachelor's or Master's degree in:
Pharmacy (B.Pharm / M.Pharm)
Biotechnology
Microbiology
Life Sciences
Biochemistry
Biomedical Engineering
Medical Laboratory Technology (MLT)
Or any other relevant Science discipline

Freshers are encouraged to apply!

What You'll Learn
✔ CDSCO Product Registration Process
✔ Medical Devices Rules (MDR), 2017
✔ ISO 13485 Documentation
✔ Technical File & Device Master File (DMF) Preparation
✔ Import & Manufacturing License Procedures
✔ Regulatory Submissions & Compliance
✔ Product Labeling & IFU Compliance
✔ Audit Documentation & Regulatory Inspections
✔ Basics of International Regulations (CE, IVDR & FDA)

Preferred Knowledge
Basic understanding of CDSCO regulations and MDR, 2017
Awareness of ISO 13485 and Good Documentation Practices (GDP)
Basic knowledge of Microsoft Office (Word, Excel, PowerPoint)

Key Skills
Strong attention to detail
Good written and verbal communication
Documentation and organizational skills
Analytical and problem-solving abilities
Team player with a willingness to learn

📩 Interested candidates can share their updated resume via LinkedIn or email.

Know someone who would be a great fit? Tag them in the comments or share this opportunity with your network!

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