Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals

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Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...

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"Top Pharma Job: Regulatory Affairs Openings at Hetero Hyderabad"

"Hetero Pharma Hiring Regulatory Affairs Specialists in Hyderabad – Apply Now"


Are you a skilled professional in Regulatory Affairs (RA) looking to boost your career with a globally recognized pharmaceutical company? Hetero, one of India’s leading pharma organizations in formulations and APIs, is inviting applications for Regulatory Affairs Specialist positions at its Jeedimetla, Hyderabad facility.

This is a golden opportunity for professionals with expertise in ANDA, CMC, MAA submissions, lifecycle management, and regulatory compliance to join a company with strong global presence.


Job Responsibilities:-

As a Regulatory Affairs Specialist at Hetero, you will be responsible for:

  • Reviewing, compiling, and submitting Abbreviated New Drug Applications (ANDA).
  • Managing Life Cycle Management (LCM) of pharmaceutical formulations.
  • Handling pre-approval and post-approval submissions.
  • Preparing and supporting Marketing Authorization Applications (MAA) for multiple global markets.
  • Ensuring compliance through CMC documentation and regulatory variations.

Required Qualifications & Experience:-

To be eligible, candidates must have:

  • Education: M.Pharm / B.Pharm / M.Sc in Pharmaceutical Sciences or a related field.
  • Experience: 3 to 9 years in Regulatory Affairs (Formulations – Emerging and ROW markets).
  • Strong understanding of CMC, global regulatory submissions, and documentation.
  • Practical exposure to regulatory submissions and lifecycle management.

Why Choose Hetero?

Joining Hetero means being part of a global pharmaceutical leader with diverse opportunities. Key benefits include:

  • Working with one of India’s top pharmaceutical companies.
  • Gaining international exposure across regulatory markets.
  • Professional growth in the Regulatory Affairs domain.
  • Competitive salary along with performance-based benefits.

How to Apply:-

Interested candidates can share their CVs directly to the recruiter:

📧 Email: chandrasekhar.r@hetero.com
Subject Line: Application For RA


FAQs:-

Q: What is the role being offered at Hetero?
A: The opening is for Regulatory Affairs Specialists at the Jeedimetla, Hyderabad facility.

Q: What is the required experience for this job?
A: Applicants should have 3 to 9 years of experience in Regulatory Affairs (Formulations).


✨ Don’t miss this opportunity to accelerate your career in Regulatory Affairs with Hetero Pharma. Apply today and take the next step toward professional growth in the global pharmaceutical industry.

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