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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“Lucent Biotech DRA Internship 2025 in Lucknow | Pharma Graduates Apply Now”

"Drug Regulatory Affairs (DRA) Internship at Lucent Biotech Limited – Lucknow | Apply Now"

(Lucent Biotech DRA Internship)

Are you a pharmacy graduate or postgraduate looking to build a career in Drug Regulatory Affairs (DRA)? Lucent Biotech Limited, a trusted name in pharmaceutical manufacturing, is offering an exciting DRA Internship in Lucknow. This program is designed to provide freshers and young professionals with hands-on training in regulatory compliance, dossier preparation, and pharma documentation.

This article covers the full details of the Lucent Biotech DRA Internship 2025, including responsibilities, qualifications, stipend, benefits, and how to apply.


Internship Overview:-

  • Position: Drug Regulatory Affairs (DRA) Intern
  • Location: Lucknow, Uttar Pradesh
  • Stipend: ₹10,000 per month
  • Duration: Minimum 6 months (extendable based on performance)

Key Responsibilities of a DRA Intern:-

As a Drug Regulatory Affairs Intern at Lucent Biotech, your role will include:

  • Assisting in regulatory dossier preparation and review.
  • Maintaining product registration files and compliance documents.
  • Coordinating with cross-functional teams to collect, compile, and organize data.
  • Keeping up-to-date with national and international regulatory guidelines.
  • Learning the end-to-end process of drug application and variation filings.

Eligibility Criteria:-

Educational Qualification:

  • B.Pharm / M.Pharm
  • Life Sciences graduates with an interest in regulatory affairs

Skills Required:

  • Strong attention to detail and accuracy
  • Basic knowledge of drug regulatory guidelines
  • Good communication and documentation skills
  • Ability to work effectively in a team environment

Why Join Lucent Biotech’s DRA Internship?

  • Gain real-world experience in Drug Regulatory Affairs.
  • Work under the mentorship of experienced regulatory professionals.
  • Earn a monthly stipend of ₹10,000.
  • Receive a certificate of internship after successful completion.
  • Build networking opportunities in the pharmaceutical industry.

How to Apply for DRA Internship at Lucent Biotech:-

Interested candidates can apply by sending their updated CV to the contact details below:

Apply soon to secure your chance to start your career in Drug Regulatory Affairs with Lucent Biotech Limited.


FAQs – Lucent Biotech DRA Internship 2025:-

1. What is the stipend for the DRA internship at Lucent Biotech?

The stipend for the DRA Internship is ₹10,000 per month.

2. Who can apply for this internship?

Candidates with a B.Pharm, M.Pharm, or Life Sciences background are eligible to apply. Freshers with an interest in regulatory affairs are also encouraged to apply.


 This internship is an excellent opportunity for pharmacy graduates who want to start their careers in Drug Regulatory Affairs. Don’t miss the chance to gain practical exposure in one of the most crucial areas of the pharmaceutical industry.

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