Eugia Pharma Walk in Regulatory Affairs

Regulatory Affairs Vacancies for M.Pharm/B.Pharm in Hyderabad

Hiring M.Pharm/B.Pharm professionals for Regulatory Affairs roles at Eugia Pharma Research Center, Hyderabad. Apply for 3–10 years experience openings.

Eugia Pharma Research Center is recruiting experienced regulatory professionals for its CMC and Post-Approval Labeling teams. These openings are suited for candidates who understand global regulatory expectations and can support submissions across major markets, including the US, EU, Canada, and RoW regions. The walk-in drive offers a focused opportunity for specialists who want to grow in a structured, compliance-driven pharmaceutical research environment with high career stability and exposure to international regulatory frameworks.

Company Overview

Eugia is part of a well-established pharmaceutical group known for its strong global footprint in sterile products, complex generics, and research-led development. The organization operates with high-quality standards supported by stringent regulatory systems and continuous innovation. The Pashamylaram research facility is structured to support development, regulatory documentation, and lifecycle management of complex formulations. Its teams work across multiple regulated markets and handle submissions that directly impact patient access to safe and effective medicines worldwide.

Job Role & Responsibilities

The Regulatory Affairs team handles documentation, submissions, and lifecycle management for CMC and Post-Approval Labeling. Depending on the designation, responsibilities include:

• Preparing, compiling, and reviewing CMC documentation
• Supporting global submissions for US, EU, Canada, and Rest of World markets
• Handling post-approval activities, supplements, variations, and labeling updates
• Coordinating with formulation, QA, and analytical teams
• Ensuring compliance with current global regulatory guidelines
• Maintaining submission timelines and responding to agency queries

These roles demand strong documentation skills, deep familiarity with regulatory expectations, and the ability to manage multiple international submissions across diverse markets.

Eligibility / Qualifications

Required education:

• M.Pharm
• B.Pharm

Relevant courses include: Pharmaceutical Technology, Regulatory Affairs, Quality Assurance, Industrial Pharmacy, Pharmaceutics, Drug Development, Biotechnology, Chemistry, Life Sciences.

Experience required: 3–10 years in Regulatory Affairs.

Preferred expertise:

• CMC documentation
• Post-Approval Labeling
• Experience with US FDA, EMA, Health Canada, and RoW submissions

Location & Salary

Location: Eugia Pharma Research Center – Pashamylaram, Hyderabad, Telangana.

Salary: As per company norms and based on relevant experience.

Application Process

Walk-in Interview Details:

Date: 23 November 2025 (Sunday)
Time: 9:00 AM to 11:00 AM
Venue: Aurobindo Pharma Ltd., Research Centre-I, Sy. No. 313, Bachupally, Hyderabad, Telangana – 500090
Contact Persons: Reshma / Shaher Banu

Candidates unable to attend may email their profiles to: Shaher.Banu@eugiapharma.com

Applicants should carry:

• Updated resume
• Educational certificates
• PAN & Aadhar
• Latest increment letter

FAQs

What experience level is required?
Candidates with 3–10 years of Regulatory Affairs experience.

Which markets will the role support?
US, EU, Canada, and Rest of World submissions.

Is CMC experience mandatory?
CMC and Post-Approval Labeling experience is preferred and strongly valued.

Can candidates apply without attending the walk-in?
Yes. Profiles can be emailed to the provided address.

Is the role documentation-heavy?
Yes. Strong technical writing and regulatory compliance skills are essential.

Summary Table

Category	Details
Company	Eugia Pharma Research Center
Vacancies	Regulatory Affairs – CMC & Post-Approval Labeling
Required Education	M.Pharm, B.Pharm
Experience	3–10 years

Tagged as: Pharma Jobs in Hyderabad