RegTech India solution Hiring Freshers For Project Management & Regulatory Affairs Roles

 

🚀 RegTech India Hiring Freshers in Project Management & Regulatory Affairs

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📌 Position Details

Company: RegTech India
Positions Available:

• Project Management Officer

• Regulatory Affairs Officer (Clinical Focus)

• Regulatory Affairs Officers (QA & Analytical Chemistry)
  Experience: 0-1 year (Freshers can apply)
  Location: Ahmedabad, Gujarat
  Qualifications: B.Pharm, M.Pharm, M.Sc
  Job Type: ✅ Verified Job
  Application Mode: Email Application

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🏢 About RegTech India Solutions

RegTech India Solutions is a dynamic organization specializing in regulatory compliance and pharmaceutical project management. We help companies transform compliance challenges into business success. Our team works on cutting-edge regulatory affairs, pharmacovigilance, clinical research, and GMP projects. We also run PharmaBharat.com, a leading platform for pharmaceutical professionals, providing industry insights and job opportunities.

📍 Address: RegTech India, 407 Shitiratna Complex, Panchvati Circle, Ellisbridge, Ahmedabad, Gujarat

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🎯 Open Positions & Responsibilities

1️⃣ Project Management Officer

📜 Qualification: B.Pharm
💼 Experience: 0-1 year

Key Responsibilities:

• Track and manage timelines across Regulatory Affairs (RA), Pharmacovigilance (PV), Clinical, and GMP projects.

• Coordinate with internal teams and clients for seamless project execution.

• Maintain project trackers, submission logs, and compliance documentation.

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2️⃣ Regulatory Affairs Officer (Clinical Focus)

📜 Qualification: M.Pharm (Clinical Pharmacy)
💼 Experience: 0-1 year

Key Responsibilities:

• Apply strong clinical pharmacy knowledge in regulatory submissions.

• Understand Modules 1-5 structure of regulatory dossiers.

• Prepare and review documents with proficiency in MS Word/Excel.

• Ensure high-quality documentation and effective communication.

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3️⃣ Regulatory Affairs Officers (QA & Analytical Chemistry)

📜 Qualification: M.Pharm (QA) / M.Sc (Analytical Chemistry)
💼 Experience: 0-1 year

Key Responsibilities:

• Strong documentation skills in Quality Assurance (QA) or Analytical Chemistry.

• Familiarity with ICH guidelines & CTD structure.

• Proficient in Excel, Word, and regulatory databases.

• Detail-oriented with strong teamwork abilities.

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🌟 Why Join RegTech India Solutions?

✅ Work on high-impact regulatory and compliance projects
✅ Gain hands-on experience in pharmaceutical regulations, clinical research, and GMP
✅ Collaborative work environment with industry experts
✅ Opportunities for professional growth and skill development

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