We’re Hiring: Regulatory Affairs Trainee – A Golden Opportunity for Freshers & Final-Year Students!

Are you a passionate M.Pharm graduate or final-year student dreaming of building a strong career in the pharmaceutical industry? Do you aspire to work in a professional environment where learning, growth, and real-time regulatory exposure go hand-in-hand? If yes, then this opportunity is tailor-made for you! 🎯

HUMANO, a reputed and growing organisation, is inviting enthusiastic and dedicated candidates to join as Regulatory Affairs Trainee at its Pune (Baner) location. This is an excellent platform for fresh minds who want to explore the dynamic world of global regulatory affairs, dossier preparation, and compliance management 🌍.

💼 Why Choose a Career in Regulatory Affairs?

Regulatory Affairs is one of the most prestigious and rapidly expanding domains in the pharmaceutical and healthcare industry. Professionals in this field act as the bridge between pharmaceutical innovation and regulatory authorities across the world. They ensure that drugs, medical devices, and healthcare products are developed, manufactured, and marketed in compliance with global quality and safety standards.

As a Regulatory Affairs Trainee, you will get exposure to: ✔️ International regulatory guidelines

✔️ Submission procedures

✔️ Documentation standards

✔️ Real-time compliance requirements

This role not only strengthens your technical expertise but also opens doors to promising growth, stability, and global career opportunities 🌐✨.

👩‍💻 Role Highlights – What Will You Do?

As part of the Regulatory Affairs team at HUMANO, you will work alongside experienced professionals and gain hands-on knowledge in regulatory activities. Your key responsibilities will include:

🔹 Supporting dossier preparation and submission activities

🔹 Assisting in regulatory documentation and maintaining compliance records

🔹 Exposure to global regulatory frameworks, including FDA, EMA, ICH, LATAM, APAC, and Middle East markets

🔹 Supporting registration activities and assisting in structured documentation

🔹 Learning and applying CTD/ACTD formats and relevant regulatory guidelines

This role is highly suitable for individuals who enjoy attention to detail, structured documentation, analytical thinking, and a willingness to learn 💡.

🎓 Eligibility Criteria – Who Can Apply?

HUMANO is looking for passionate learners with the right academic background and professional attitude. The eligibility requirements are:

🎓 Qualification: M.Pharm (Freshers & Final-year students are welcome)

📚 Knowledge: Basic understanding of CTD/ACTD & ICH guidelines is preferred

🗂️ Skills: Strong communication, documentation, and organisational skills

💻 Technical Skills: Familiarity with MS Office and Adobe Acrobat

📍 Location: Baner, Pune

If you have a keen interest in Regulatory Affairs and a desire to work in a structured, professional environment, this is your moment to shine ⭐.

🌍 Exposure to Global Regulatory Systems

One of the biggest advantages of this role is the opportunity to understand regulatory frameworks across different regions. You will gain exposure to:

🌎 FDA (United States) – Understanding compliance, approval pathways, and submission requirements

🇪🇺 EMA (Europe) – Learning structured regulatory approaches and documentation standards

📜 ICH Guidelines – Implementing globally harmonised regulatory principles

🌏 APAC, LATAM & Middle East Markets – Exploring diverse regulatory landscapes and submission processes

This experience will significantly enhance your professional value and help you stand out in the competitive pharmaceutical industry 💼🔥.

🏢 About the Work Environment

At HUMANO, you will be part of a supportive and collaborative environment where learning is encouraged and innovation is appreciated. The organisation believes in nurturing fresh talent and helping them develop strong professional foundations.

You’ll work with experienced mentors, gain real-time project exposure, and build an impressive regulatory skill set that will shape your future career 🚀.

📍 Job Location

📌 Baner, Pune, Maharashtra

A vibrant professional hub with excellent opportunities, connectivity, and a dynamic work culture.

📞 How to Apply?

If you’re excited to begin your journey in Regulatory Affairs and want to build a rewarding career, don’t miss this opportunity! Submit your application and take the first step toward success.

📧 Email: jobs@humanoforte.com

📱 Contact: +91 8484947342

✨ Final Words

A career opportunity like this doesn’t come often, especially for freshers and students. If you are serious about your professional growth and passionate about contributing to the pharmaceutical world, apply today! This is your chance to learn, grow, and build a successful future in Regulatory Affairs 🌟