Swiss Parenteral Hiring Regulatory Affairs
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Swiss Parenteral Limited?
- FAQs
- Summary Table
B.Pharm/M.Pharm Regulatory Affairs Openings – Swiss Parenteral Ltd, Ahmedabad
Apply for Executive–Asst. Manager roles in Regulatory Affairs at Swiss Parenteral Ltd, Ahmedabad. 3–8 yrs experience in Parenteral Products.
Swiss Parenteral Limited, a trusted name in sterile and parenteral formulations, is inviting experienced professionals to join its International Regulatory Affairs team at its corporate office in Ahmedabad. This is a golden opportunity for pharma professionals with a strong background in Regulatory Affairs, Dossier Preparation, and CTD/ACTD/ECTD formats to work with a globally recognized company.
Company Overview
Swiss Parenteral Limited is a well-established pharmaceutical manufacturer known for its excellence in sterile injectables and parenteral products. With a strong presence across Africa, LATAM, MENA, and APAC markets, the company operates under stringent global standards including WHO-GMP, PIC/S, and ISO certifications. Swiss Parenteral has earned industry credibility through consistent quality, technological innovation, and compliance-driven manufacturing practices.
By joining Swiss Parenteral, you’ll be part of a progressive organization that focuses on developing life-saving medicines and expanding access to affordable healthcare worldwide.
Job Role & Responsibilities
The company is looking for Executives to Assistant Managers for its Regulatory Affairs (International Markets) division. The selected candidates will play a crucial role in ensuring the company’s products meet global regulatory standards and achieve timely approvals.
Key Responsibilities:
- Preparation, compilation, and submission of regulatory dossiers (CTD/ACTD/ECTD formats).
- Review of technical documents for product registration across ROW regions (Africa, LATAM, MENA, APAC).
- Coordinate with cross-functional departments like QA, QC, and Production for regulatory compliance.
- Respond to regulatory queries and deficiency letters from health authorities.
- Maintain updated knowledge of international regulatory requirements and guidelines.
- Ensure timely renewals and variations of registered products.
Eligibility / Qualifications
Educational Qualification:
- B.Pharm / M.Pharm (Pharmaceutical Sciences, Regulatory Affairs, Pharmaceutics, Quality Assurance)
Experience Required:
- 3 to 8 years of relevant experience in Regulatory Affairs for Parenteral Products.
Technical Skills:
- Hands-on experience in CTD, ACTD, and eCTD dossier preparation and review.
- Knowledge of regulatory pathways across multiple markets (Africa, LATAM, MENA, APAC).
- Understanding of QMS, documentation, and regulatory compliance.
Important Note: Freshers are not eligible for this position.
Location & Salary
Location: Sindhu Bhavan, Ahmedabad, Gujarat
Industry: Pharmaceuticals (Injectables/Parenterals)
Employment Type: Full-Time
Salary: Competitive – commensurate with experience and skillset.
Application Process
Interested candidates meeting the above criteria can apply directly by sharing their updated resume via email at:
hroffice1@swiss.in
Apply before 20 October 2025 to secure your chance to join a reputed global pharmaceutical organization.
Why Join Swiss Parenteral Limited?
- Work in a USFDA and WHO-GMP-compliant facility.
- Be part of a company with a global export footprint across 70+ countries.
- Gain exposure to international regulatory frameworks and dossier submissions.
- Competitive pay, supportive work environment, and long-term career growth opportunities.
FAQs
1. Who can apply for this Swiss Parenteral Ltd Regulatory Affairs opening?
Candidates with 3–8 years of experience in Regulatory Affairs for Parenteral products and holding B.Pharm or M.Pharm degrees can apply.
2. Is this role open for freshers?
No. This opportunity is only for experienced professionals.
3. What skills are required for this position?
Hands-on experience in CTD/ACTD/eCTD dossier preparation, regulatory submission, and product registration for ROW markets.
4. Where is the job location?
The position is based at Swiss Parenteral Ltd, Sindhu Bhavan, Ahmedabad.
5. What is the deadline to apply?
Candidates are advised to apply before 20th October 2025 for priority consideration.
Summary Table
| Category | Details |
|---|---|
| Company | Swiss Parenteral Limited |
| Vacancies | Executive to Assistant Manager – Regulatory Affairs |
| Required Education | B.Pharm, M.Pharm |
| Experience | 3 to 8 Years in Regulatory Affairs (Parenterals) |
| Location | Sindhu Bhavan, Ahmedabad |
| Application Email | hroffice1@swiss.in |
| Last Date to Apply | 20 October 2025 |
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