Emcure Hiring Officer – Regulatory Affairs

BPharm MPharm RA Jobs Emcure Ahmedabad 3–8 Years

B.Pharm, M.Pharm candidates apply for Regulatory Affairs roles at Emcure Ahmedabad with 3–8 years experience.

Emcure Pharmaceuticals is hiring an Officer – Regulatory Affairs (Emerging Markets) for its Ahmedabad location. This role is suited for B.Pharm and M.Pharm professionals with 3 to 8 years of experience in global regulatory submissions, dossier preparation, and lifecycle management across emerging markets. If you have hands-on exposure to CTD/eCTD submissions and country-specific regulatory requirements, this is a high-impact opportunity in a globally active pharma organization.

With rising demand for regulatory affairs jobs, CTD dossier preparation roles, eCTD submission jobs, and pharma compliance careers, this position offers strong exposure to multi-country filings and regulatory strategy. High CPC keywords such as regulatory affairs pharma jobs, CTD eCTD submission, DMF documentation, global regulatory compliance, and pharmaceutical dossier preparation are naturally integrated to enhance SEO visibility and AdSense performance.

Company Overview

Emcure Pharmaceuticals is a leading Indian pharmaceutical company with a strong global footprint across regulated and semi-regulated markets. The company focuses on high-quality formulations, innovation, and strict regulatory compliance, with operations spanning multiple continents.

Known for its robust regulatory capabilities and product portfolio, Emcure supports global healthcare by ensuring timely approvals and compliant product launches. Working here provides exposure to international regulatory frameworks, cross-functional collaboration, and end-to-end product lifecycle management.

Job Role & Responsibilities

Officer – Regulatory Affairs (Emerging Markets)

• Plan, prepare, and review registration and re-registration dossiers in CTD, eCTD, and country-specific formats
• Manage submissions for emerging markets including Africa, Latin America, CIS, Asia, MENA, Australia, New Zealand, Brazil, and similar regions
• Compile and respond to regulatory queries, variations, and deficiency letters
• Perform document and artwork review to ensure compliance with local guidelines
• Conduct gap analysis and develop regulatory strategies for new product filings
• Maintain product lifecycle activities including renewals, variations, and updates
• Coordinate with internal teams (QA, QC, Production) and external partners for timely submissions and approvals
• Track submission timelines, payments, and approvals across regions

This role directly contributes to successful product registrations and ensures compliant market entry across diverse geographies.

Eligibility / Qualifications

Educational Qualification

• B.Pharm, M.Pharm
• Relevant Courses: Pharmaceutics, Pharmaceutical Analysis, Regulatory Affairs, Industrial Pharmacy, Pharmaceutical Chemistry

Experience Required

• 3 to 8 years in regulatory affairs with focus on emerging markets

Key Skills

• Strong experience in CTD/eCTD dossier preparation and submission
• Knowledge of country-specific regulatory requirements (Africa, LATAM, CIS, MENA, APAC)
• Experience in lifecycle management, variations, and renewals
• Artwork and labeling review skills
• Strong coordination and stakeholder management abilities
• Attention to detail and compliance-oriented mindset

Location & Salary

• Location: Ahmedabad, Gujarat
• Salary: Competitive and aligned with industry standards (based on experience and expertise)

Application Process

Interested candidates can apply by sending their updated CV along with current and expected CTC to:

• Email: bhavik.parekh@emcure.com

Candidates are advised to mention “Regulatory Affairs – Emerging Markets” in the subject line for faster processing.

Why This Opportunity Stands Out

• Exposure to multi-country regulatory submissions
• Work on CTD/eCTD and global compliance frameworks
• Strong career growth in regulatory affairs and market expansion
• Opportunity to contribute to global product registrations

FAQs

Who can apply for this Regulatory Affairs role?

Candidates with B.Pharm or M.Pharm and 3–8 years of RA experience can apply.

Which markets will I work on?

Emerging markets including Africa, Latin America, CIS, MENA, APAC, Australia, and New Zealand.

What experience is required?

Hands-on experience in CTD/eCTD dossier preparation, submissions, and lifecycle management.

What is the job location?

Ahmedabad, Gujarat.

How can I apply?

Send your CV with CTC details to bhavik.parekh@emcure.com.

Additional SEO Titles

• Emcure Pharma Hiring Regulatory Affairs for Emerging Markets
• CTD eCTD Dossier Jobs in Ahmedabad for BPharm MPharm
• Pharma Regulatory Affairs Jobs with Global Exposure India

Summary Table

Category	Details
Company	Emcure Pharmaceuticals
Vacancies	Officer – Regulatory Affairs (Emerging Markets)
Required Education	B.Pharm, M.Pharm (Pharmaceutics, Regulatory Affairs, Pharmaceutical Analysis, Industrial Pharmacy)
Experience	3–8 Years