"Swiss Parenterals Hiring for Regulatory Affairs Roles | B.Pharm & M.Pharm Jobs in Ahmedabad"
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| (Swiss Parenteral Hiring 2025) |
Are you a skilled regulatory affairs professional looking to grow in the global pharmaceutical sector? Swiss Parenteral Limited, one of India’s reputed manufacturers of sterile and parenteral products, is inviting applications for Executive to Assistant Manager positions in their Regulatory Affairs Department, located at Sindhu Bhavan, Ahmedabad.
This is a golden opportunity for B.Pharm and M.Pharm graduates with hands-on experience in CTD, ACTD, eCTD, and dossier preparation for international markets such as Africa, LATAM, MENA, and APAC.
About Swiss Parenteral Limited:-
Swiss Parenterals is a globally recognised pharmaceutical company committed to delivering high-quality parenteral formulations. With a strong presence in regulated and semi-regulated markets, the company ensures compliance with stringent international standards and continues to expand its footprint across multiple continents.
Joining Swiss Parenterals means becoming part of a professional team focused on quality, innovation, and regulatory excellence.
Job Overview:-
- Position: Executive / Sr. Executive / Assistant Manager
- Department: Regulatory Affairs
- Location: Sindhu Bhavan, Ahmedabad, Gujarat
- Industry: Pharmaceuticals (Parenteral Products)
- Experience Required: 3–8 Years
- Qualification: B.Pharm / M.Pharm
- Employment Type: Full-time (On-site)
Key Responsibilities:-
As part of the Regulatory Affairs team, selected candidates will:
- Prepare, review, and compile CTD, ACTD, and eCTD dossiers for global regulatory submissions.
- Ensure regulatory compliance with international guidelines and requirements.
- Collaborate with cross-functional departments for data collection, documentation, and dossier submission.
- Maintain up-to-date knowledge of regulatory requirements in Africa, LATAM, MENA, and APAC markets.
- Support audit activities and prepare responses for regulatory queries.
- Review product labelling and artwork for accuracy and compliance.
Eligibility Criteria:-
- Education: B.Pharm or M.Pharm recognised university.
- Experience: 3–8 years in core regulatory affairs, preferably in parenteral product manufacturing.
- Technical Skills:
- Strong knowledge of CTD, ACTD, and eCTD dossier preparation and review.
- Understanding of GMP, WHO, and international regulatory guidelines.
- Excellent documentation and coordination skills.
- Note: Freshers are not eligible for this role.
Salary and Benefits:-
- Attractive CTC in the range of ₹5,00,000 – ₹10,00,000 per annum (based on experience).
- Work with a reputed pharmaceutical company specialising in parenteral formulations.
- Opportunity for global exposure in international regulatory markets.
- Professional growth in Regulatory Affairs and access to industry-leading training programs.
- Supportive, collaborative work culture with career advancement opportunities.
How to Apply:-
Interested and eligible candidates can send their updated CVs to the official HR email:
📧 hroffice1@swiss.in
Mention “Application for Regulatory Affairs – Ahmedabad” in the subject line.
Ensure your CV clearly highlights your experience in CTD, ACTD, eCTD, and dossier preparation.
Frequently Asked Questions (FAQs):-
Q1. What are the target markets for this role?
This position focuses on ROW markets, including Africa, LATAM, MENA, and APAC regions.
Q2. What is the required experience?
Candidates must have 3–8 years of experience in Regulatory Affairs, specifically related to parenteral products and dossier submissions.
Q3. Are freshers eligible for this job?
No, this position is open only for experienced professionals.
Conclusion:-
If you’re passionate about ensuring global regulatory compliance and want to work with one of India’s fastest-growing pharmaceutical firms, Swiss Parenteral Limited is the right place for you.
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