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Aurobindo Pharma RA Jobs 2026 | Regulatory Affairs US EU Markets | Hyderabad | 2-12 Years | B.Pharm M.Pharm

Aurobindo Pharma RA Jobs 2026 | Regulatory Affairs US EU Markets | Hyderabad | 2-12 Years | B.Pharm M.Pharm

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📢 Aurobindo Pharma Hiring 2026: Regulatory Affairs – US & EU Markets | Hyderabad | 2-12 Years Exp | Apply Now 📢

Aurobindo Pharma RA Recruitment 2026: Aurobindo Pharma Limited is hiring for Regulatory Affairs – US & EU Markets at APLRC-1, Hyderabad. Positions available in ANDA Filing, Post Approvals, CMC, LCM, SPD-Topical/Derma. Experience: 2-12 Years. Qualification: B.Pharm / M.Pharm. Preferred candidates with hands-on experience in US & EU Formulations RA.

📋 About the Company

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India. The company manufactures generic pharmaceuticals and active pharmaceutical ingredients with a strong global presence in regulated markets.

📋 Job Details

Company Name Aurobindo Pharma Limited
Department Regulatory Affairs – US & EU Markets
Location APLRC – 1, Hyderabad, Telangana
Industry Pharmaceutical Manufacturing – Generic & API

📋 Available Positions – US Market

1. RAD-US – ANDA Filing

  • ✔ Experience: 4.5 to 6 Years in RAD-US market
  • ✔ Qualification: B.Pharm / M.Pharm – Regulatory Affairs / Pharmaceutics
  • ✔ Focus: ANDA Submissions and Filings

2. RAD-US – Post Approvals LCM

  • ✔ Experience: 4.5 to 6 Years in RAD-US market
  • ✔ Qualification: B.Pharm / M.Pharm – Regulatory Affairs / Pharmaceutics
  • ✔ Focus: Post Approval Lifecycle Management

3. RAD-US – SPD – Topical / Derma

  • ✔ Experience: 4.5 to 6 Years in RAD-US market
  • ✔ Qualification: B.Pharm / M.Pharm – Regulatory Affairs / Pharmaceutics
  • ✔ Focus: Topical and Derma Product Regulatory

📋 Available Positions – EU Market

1. RA_EU – Pre & Post Approvals

  • ✔ Experience: 2 to 5 Years in EU-CMC – Post Approvals
  • ✔ Qualification: M.Pharm – Regulatory Affairs / Pharmaceutics / Analysis / QA
  • ✔ Focus: EU Pre and Post Approval Activities

2. RA_EU – CMC LCM

  • ✔ Experience: 8 to 12 Years in EU-CMC-LCM
  • ✔ Qualification: M.Pharm – Regulatory Affairs / Pharmaceutics / Analysis / QA
  • ✔ Focus: EU CMC Lifecycle Management

✅ Who Can Apply?

  • ✔ Candidates with B.Pharm / M.Pharm in Regulatory Affairs, Pharmaceutics, Analysis, Quality Assurance
  • ✔ US Market: 4.5 to 6 years experience in RAD-US
  • ✔ EU Market: 2 to 5 years for Post Approvals, 8 to 12 years for CMC-LCM
  • ✔ Preferred: Hands-on experience with Formulations RA in US and EU markets

📍 Work Location

APLRC – 1, Hyderabad, Telangana

📝 How to Apply

Interested candidates can share their updated resume to the respective email ID based on market:

US Market Applications Sreeja.Yangam@aurobincto.com
EU Market Applications Pooja.Uppalapati@aurobindo.com
Subject Apply – RA Position – Market – Your Name

❓ FAQs

Q1: What positions are open at Aurobindo Pharma?

A: Regulatory Affairs positions for US Market: ANDA Filing, Post Approvals, SPD and EU Market: Pre/Post Approvals, CMC-LCM

Q2: What is the required experience?

A: US: 4.5-6 years. EU: 2-5 years for Post Approvals, 8-12 years for CMC-LCM

Q3: What qualification is required?

A: B.Pharm / M.Pharm in Regulatory Affairs, Pharmaceutics, Analysis, Quality Assurance

Q4: What is the job location?

A: APLRC-1, Hyderabad

Tags: Aurobindo Pharma Jobs, Regulatory Affairs Jobs, RA Jobs, US RA Jobs, EU RA Jobs, ANDA Filing Jobs, CMC Jobs, LCM Jobs, Hyderabad Jobs, B.Pharm Jobs, M.Pharm Jobs, 2026

⚠️ Note: Eligible candidates with US/EU Regulatory Affairs experience should email resume to respective HR. Mention position and market in subject line.

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