Exciting Openings in Regulatory Affairs at Swiss Parenteral Limited-Apply before 4th November 2025

About Swiss Parenteral Limited

Swiss Parenteral Limited is a leading manufacturer of high-quality parenteral formulations, committed to delivering safe and effective pharmaceutical products to global markets. With a strong presence across Africa, LATAM, MENA, and APAC regions, Swiss Parenteral continues to set benchmarks in sterile manufacturing and global regulatory compliance.

We are now inviting applications for Executive to Assistant Manager – Regulatory Affairs positions at our Sindhu Bhavan, Ahmedabad office. This is an exciting opportunity for experienced professionals to play a vital role in driving international regulatory submissions and compliance excellence.

🌍 Position Overview

Are you passionate about global pharmaceutical regulations and dossier management?
Join our Regulatory Affairs team and contribute to the preparation, review, and submission of CTD, ACTD, and eCTD dossiers for international markets. This role offers exposure to global health authorities and provides the chance to work in a fast-paced, compliance-driven environment.

Key Responsibilities

• Prepare, review, and compile CTD, ACTD, and eCTD dossiers for regulatory submissions in ROW markets (Africa, LATAM, MENA, APAC).

• Ensure all documentation meets regulatory and quality standards for parenteral products.

• Collaborate with cross-functional teams—formulation, QA, QC, and production—for data collection and dossier completion.

• Stay updated with international regulatory guidelines and adapt submission strategies accordingly.

• Support regulatory audits and inspections by providing required documentation and reports.

• Maintain a strong compliance focus and ensure timely submission of dossiers for product registration and renewals.

🎓 Qualifications & Skills

Education:

• B.Pharm or M.Pharm from a recognized institution.

Experience:

• 3–8 years of experience in Regulatory Affairs, specifically in parenteral or sterile formulations.

• Strong knowledge and hands-on experience with CTD, ACTD, eCTD, and dossier preparation/review.

Skills & Competencies:

• Understanding of global regulatory frameworks across Africa, LATAM, MENA, and APAC.

• Excellent communication, documentation, and organizational skills.

• Ability to manage multiple projects and meet tight deadlines.

• Proficiency in MS Office and regulatory submission tools.

❌ Note: Freshers are not eligible for this position.

💼 Why Join Swiss Parenteral Limited?

• Opportunity to work with a global leader in parenteral formulations.

• Competitive compensation: INR 5,00,000 – 10,00,000 per annum, based on experience.

• Professional development and exposure to international regulatory environments.

• Collaborative, inclusive, and growth-oriented workplace in Ahmedabad.

• Access to cutting-edge tools and continuous learning in pharmaceutical compliance.

📝 How to Apply

If you’re ready to grow your career in international regulatory affairs, send your updated CV to
📧 hroffice1@swiss.in
with the subject line: “Application for Executive / Assistant Manager – Regulatory Affairs”.

📅 Application Deadline: November 4, 2025
📍 Location: Sindhu Bhavan, Ahmedabad, Gujarat

🌟 Be Part of a Global Mission

Join Swiss Parenteral Limited and contribute to our mission of ensuring global access to safe, effective, and high-quality pharmaceutical solutions. Your expertise can help make a world of difference in patient care.

Swiss Parenteral Limited – Where Quality Meets Compliance.