Start your career in Regulatory Affairs! Morepen Laboratories Ltd. is hiring M.Sc. and M.Pharm freshers at its API plant in Parwanoo, Himachal Pradesh. Apply now for an exciting pharma opportunity.

🚀 Start Your Pharma Career with Morepen Laboratories Ltd. – Fresher Opportunities in Drug Regulatory Affairs

Are you a recent M.Sc. or M.Pharm graduate looking for an exciting opportunity in the pharmaceutical industry? Do you aspire to work in one of the most essential and intellectually rewarding departments of a global pharmaceutical company? If so, Morepen Laboratories Ltd. invites you to begin your career in Drug Regulatory Affairs (DRA) at our API manufacturing facility in Parwanoo, Himachal Pradesh.

🏢 About Morepen Laboratories Ltd.

Morepen Laboratories Ltd. is a leading name in the Indian pharmaceutical sector with over 30 years of industry experience. We specialize in Active Pharmaceutical Ingredients (API), Finished Dosage Forms, and Diagnostics. Our manufacturing plants comply with global standards such as USFDA, EDQM, WHO-GMP, and more. Our consistent growth has been fueled by innovation, quality, and a dedicated team of professionals.

Our API facility in Parwanoo (Himachal Pradesh) is one of the most advanced in the country, built to meet stringent international regulatory norms. With a culture that values learning, integrity, and innovation, Morepen is the ideal platform for fresh graduates to launch their pharmaceutical careers.

📌 Job Role: Regulatory Affairs – Fresher Opportunity

✅ Designation:

Trainee / Officer – Regulatory Affairs (DRA)

✅ Department:

Drug Regulatory Affairs – API Division

✅ Location:

Parwanoo, Himachal Pradesh

✅ Qualification Required:

• M.Sc. (Master of Science – Chemistry, Biotechnology, or related fields)

• M.Pharm. (Master of Pharmacy – Pharmaceutical Chemistry or related specialization)

✅ Experience Required:

Freshers (0 years) – Recent pass-outs or graduates of 2023–2025

💼 Why Choose a Career in Drug Regulatory Affairs?

The Regulatory Affairs department is the nerve center of pharmaceutical compliance. It acts as a bridge between pharmaceutical science and global health authorities. Here’s why starting your career in Regulatory Affairs is a smart move:

🌍 Global Exposure

You’ll gain insight into regulatory frameworks such as USFDA, MHRA, EMA, TGA, and WHO guidelines—knowledge that is valuable across the globe.

🧠 Continuous Learning

You will stay up-to-date with the latest pharmaceutical regulations, product documentation processes, and scientific innovations.

🤝 Cross-Functional Interaction

The role offers collaboration with R&D, QA, QC, production, and marketing—enhancing both technical and managerial skills.

📈 Career Growth

A career in Regulatory Affairs provides a stable, well-respected, and high-paying career path, with opportunities for rapid advancement.

🔍 Key Responsibilities (As You Grow)

As a fresher, you’ll be trained and mentored by experienced professionals. You’ll learn to:

• Prepare regulatory dossiers for submission to various global markets

• Compile and review technical documents, DMFs (Drug Master Files), and CTDs (Common Technical Documents)

• Support in responding to regulatory queries

• Coordinate with cross-functional teams for timely submission of documents

• Stay updated on international regulatory changes and compliance requirements

• Maintain electronic and hard copy documentation systems

🎯 Who Should Apply?

We are looking for fresh, enthusiastic, and detail-oriented individuals who have a passion for pharmaceutical sciences and are ready to build a long-term career in Regulatory Affairs.

✅ Ideal Candidate Traits:

• Strong academic background in Chemistry or Pharmacy

• Basic understanding of ICH guidelines and regulatory concepts (training will be provided)

• Good communication and documentation skills

• Eagerness to learn and contribute in a collaborative environment

• Ability to handle multiple tasks with attention to detail

🌟 What Makes Morepen the Right Place for Freshers?

At Morepen, you’re not just an employee—you’re part of a mission to make healthcare accessible, affordable, and globally compliant. We offer:

• ✳ Structured training programs for freshers

• ✳ Mentorship from senior regulatory professionals

• ✳ Exposure to international regulatory processes

• ✳ A positive, ethical, and inclusive work culture

• ✳ Growth-oriented career paths in Regulatory Affairs, Quality Assurance, and beyond

📍 About the Job Location – Parwanoo, Himachal Pradesh

Our API plant is located in Parwanoo, a serene industrial town in Solan District, Himachal Pradesh, close to Chandigarh. The site is well connected by road and offers a clean, green, and peaceful environment, perfect for professionals starting their career in pharma manufacturing and compliance.

📩 How to Apply

If you’re ready to begin a promising career with a company that’s committed to excellence and innovation, we encourage you to apply today.

📧 Send your updated resume to: aashish.gupta@morepen.com

📂 Subject Line: Application for Fresher – Regulatory Affairs – [Your Name]

💬 Employee Testimonials

“I joined Morepen as a fresher in Regulatory Affairs and within a year, I got exposure to global regulatory documentation and audits. It’s a great place to grow.”
— Sonal R., Regulatory Affairs Officer

“The training provided at Morepen helped me bridge the gap between theory and real-world pharmaceutical compliance.”
— Amit K., Executive – DRA

Take Your First Step with Morepen Today

Joining Morepen Laboratories Ltd. means becoming a part of a company that values scientific rigor, ethical practices, and continuous development. If you’re a fresher with a degree in M.Sc. or M.Pharm., and aspire to grow in Regulatory Affairs, this opportunity is crafted just for you.

Don’t wait. Apply now and kick-start your professional journey in one of the most critical and promising fields of the pharmaceutical industry!