Aurobindo Pharma has announced Regulatory Affairs job opportunities in Hyderabad for professionals handling US and EU markets. The openings are focused on regulatory submissions, post-approval activities and CMC-related work.

The work location mentioned in the hiring announcement is APLR C-1, Hyderabad, India. Candidates with relevant Regulatory Affairs experience can apply through email using the respective contact details given below.

Aurobindo Pharma Regulatory Affairs Jobs – Overview

US Market Regulatory Affairs Jobs

For the US Market, Aurobindo Pharma is looking for candidates with experience in regulatory activities related to US submissions.

Requirements

• Experience with RAD-US ANDA Filing
• Experience with RAD-US SPD-Topical/Derma
• Candidates with approximately 4 to 6 years of experience in the US regulatory market are preferred.
• B.Pharm or M.Pharm qualification is required.
• Specialization/background in Regulatory Affairs or Pharmaceutics is preferred.

Key Responsibilities

Selected candidates may be involved in preparing and reviewing regulatory submissions, coordinating documentation and supporting regulatory activities for the US market.

The role may also involve working with cross-functional teams to ensure submissions and regulatory documents meet applicable requirements.

EU Market Regulatory Affairs Jobs

The EU Market openings are aimed at professionals experienced in EU regulatory activities, including post-approval and CMC-related work.

Requirements

Candidates may be considered for different experience levels, including:

• 2 to 5 years of experience in EU CMC and post-approval activities.
• 8 to 12 years of experience in EU CMC and LCM activities.
• M.Pharm qualification.
• Specialization/background in Regulatory Affairs, Pharmaceutics, Analysis, Regulatory Affairs or Quality Assurance is preferred.

Key Responsibilities

The selected professionals may handle EU regulatory submissions and post-approval activities, coordinate CMC documentation and support lifecycle management activities.

The position may require close coordination with regulatory, quality, analytical and other cross-functional teams.

Educational Qualification

The qualification requirements vary by market and position:

• B.Pharm / M.Pharm for the US Market roles.
• M.Pharm for the EU Market roles.
• Relevant specialization or experience in Regulatory Affairs, Pharmaceutics, Analysis or Quality Assurance can be advantageous.

Experience Required

Experience requirements depend on the specific Regulatory Affairs opening:

• US Market: approximately 4–6 years
• EU CMC/Post-Approval: approximately 2–5 years
• EU CMC/LCM: approximately 8–12 years

Candidates should carefully match their experience with the relevant market and role before applying.

Salary and Benefits

The hiring announcement does not mention a specific salary package or detailed benefits. Compensation is therefore expected to depend on the candidate’s qualifications, relevant experience and the position offered.

For experienced Regulatory Affairs professionals, the final package may be negotiated during the recruitment process.

Job Location

Aurobindo Pharma Regulatory Affairs jobs are based at APLRC-1, Hyderabad, Telangana, India.

How to Apply

Interested and eligible candidates can send their updated CV to the appropriate email address according to their market expertise.

For US Market:
Sreeja.Yangam@aurobindo.com

For EU Market:
Pooja.Uppalapati@aurobindo.com

Candidates should mention their relevant Regulatory Affairs experience and market expertise clearly in their CV before applying.

Important Note for Candidates

This recruitment announcement does not provide a specific last date for applications. Since the application process is through email, candidates can submit their CVs using the respective email addresses and should apply as early as possible.

Candidates should verify their qualification, experience and market-specific expertise before submitting their application.