Aurobindo Pharma Hiring 30 (Regulatory Affairs – EU Market)

M.Pharm Regulatory Affairs Openings | Aurobindo Pharma Hyderabad

Apply for Regulatory Affairs positions at Aurobindo Pharma, Hyderabad. 30 openings for M.Pharm candidates with 3–6 years experience.

Aurobindo Pharma is inviting skilled Regulatory Affairs professionals to join its Formulation R&D team in Hyderabad, focusing on EU Market submissions. This is a golden opportunity for M.Pharm graduates with a passion for regulatory science and pharmaceutical innovation to contribute to global healthcare.

Company Overview

Aurobindo Pharma Limited is a leading global pharmaceutical company headquartered in Hyderabad, India. With a strong presence in over 150 countries, Aurobindo is known for its innovation, quality, and regulatory compliance. The company offers a wide range of generics, biosimilars, and specialty products, making a significant impact on global healthcare delivery.

Job Role & Responsibilities

As a Regulatory Affairs Professional – EU Market (Formulation R&D), you will:

• Prepare and review technical documents for EU submissions (Modules 2 & 3 – Quality Module).
• Interpret and apply EU regulatory guidelines (ICH, EMA).
• Manage post-approval variations for EU submissions.
• Review plant-related QA documentation.
• Collaborate cross-functionally with QA, R&D, and manufacturing teams.
• Ensure timely and compliant regulatory filings to support product approvals.

Eligibility / Qualifications

• Education: M. Pharm in Pharmaceutics, Pharmaceutical Analysis, or related fields.
• Experience: 3–6 years in FRD/FARD/QA with at least 1 year in Regulatory Affairs (EU Market preferred).
• Technical Skills: Strong knowledge of EU Module 2 & 3, ICH and EMA guidelines.
• Soft Skills: Excellent communication, documentation, and regulatory interpretation abilities.

Location & Salary

• Job Location: Hyderabad, Telangana (India).
• Compensation: Salary as per industry standards, along with growth opportunities in a global pharma leader.

Application Process

Interested candidates can apply by sending their updated resume to:

Email: Pooja.Uppalapati@aurobindo.com
Subject Line: Application for EU Market

Referrals are welcome.

Why Join Aurobindo Pharma?

• Opportunity to work in a global top-tier pharmaceutical company.
• Exposure to international regulatory frameworks (EU, US, emerging markets).
• Career growth in a dynamic and innovation-driven environment.
• Contribute to healthcare advancements through compliant regulatory processes.

FAQs

1. What is the qualification required for Aurobindo Pharma Regulatory Affairs roles?
Candidates must hold an M. Pharm in Pharmaceutics, Pharmaceutical Analysis, or related fields with relevant experience.

2. How many years of experience are required?
Applicants should have 3–6 years of FRD/FARD/QA experience, with at least 1 year in EU Regulatory Affairs.

3. Where is the job location?
The openings are based at Hyderabad, Telangana.

4. Does the role involve EU regulatory filings only?
Yes, the primary focus is on EU Market regulatory submissions, specifically handling Modules 2 & 3.

5. How can I apply?
Send your CV to Pooja.Uppalapati@aurobindo.com with the subject line “Application for EU Market”.

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