Swiss Walk-in Regulatory Affairs Officer–Executive
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs – ROW / EU Market
- Eligibility / Qualifications
- Educational Requirements
- Experience Criteria
- Location & Salary
- Walk-In Interview Details
- Date & Time
- Interview Venue
- Application Process
- SEO-Optimized Job Title Variations
- Why Build Your Career with Swiss Parenterals
- FAQs
- Who can attend this walk-in interview?
- Is parenteral experience mandatory?
- Which markets will this role handle?
- Can I apply by email instead of attending the walk-in?
- What documents should I carry for the interview?
B.Pharm M.Pharm Regulatory Jobs | Swiss Ahmedabad
Swiss Parenterals hiring Regulatory Affairs Officer–Executive in Ahmedabad. B.Pharm, M.Pharm eligible. Walk-in interview.
Swiss Parenterals Ltd. is conducting a walk-in interview for experienced Regulatory Affairs professionals to support its expanding international regulatory operations. The hiring is focused on Regulatory Affairs roles handling ROW and EU markets, with direct involvement in dossier preparation, deficiency management, and global regulatory submissions. These positions are ideal for candidates with hands-on exposure to parenteral dosage forms and strong regulatory documentation expertise.
This opportunity allows professionals to work in a globally regulated pharmaceutical environment where regulatory compliance directly impacts patient safety and access to injectable medicines across multiple international markets.
Company Overview
Swiss Parenterals Ltd. is a globally recognized pharmaceutical company specializing in sterile injectable and parenteral dosage forms. With a strong presence across regulated and semi-regulated markets, the company supports healthcare systems worldwide through compliant, high-quality injectable products.
Driven by the philosophy of empowering growth through collective strengths, Swiss Parenterals maintains stringent regulatory, quality, and compliance standards. Its regulatory teams play a crucial role in ensuring timely approvals and lifecycle management of parenteral products across Africa, CIS, ASEAN, LATAM, MENA, and EU regions.
Job Role & Responsibilities
Regulatory Affairs – ROW / EU Market
The Regulatory Affairs professional will be responsible for end-to-end regulatory documentation and submission activities for global markets.
Key responsibilities include:
- Preparation, review, and approval of regulatory dossiers in CTD, ACTD, eCTD, and national formats
- Review of technical, quality, and compliance documents for regulatory submissions
- Preparation of responses to regulatory authority queries and deficiencies
- Coordination with cross-functional teams including QA, QC, R&D, and manufacturing
- Leading deficiency response strategies and timely submissions
- Supporting lifecycle management and variation submissions
Strong understanding of regulatory guidelines and injectable product documentation is essential for this role.
Eligibility / Qualifications
Educational Requirements
- B.Pharm
- M.Pharm
Relevant courses include: Regulatory Affairs, Pharmaceutics, Pharmaceutical Technology, Industrial Pharmacy, Quality Assurance, Clinical Regulatory Sciences
Experience Criteria
- 2–4 years of relevant experience in Regulatory Affairs
- Mandatory exposure to parenteral dosage forms
- Experience handling ROW and/or EU regulatory submissions
Location & Salary
Work location: Ahmedabad, Gujarat.
Salary will be offered based on experience, regulatory expertise, and interview performance. Compensation is competitive and aligned with industry standards for regulatory affairs professionals handling international markets.
Walk-In Interview Details
Date & Time
- Date: 1 February 2026 (Sunday)
- Time: 10:30 AM to 03:30 PM
Interview Venue
Eris, Shilp Accord,
Opp. Times Square-II,
Ramdas Road, Near Gwalia Bloom,
Sindhu Bhavan Marg,
Bodakdev, Ahmedabad, Gujarat – 380054
Application Process
Interested candidates can attend the walk-in interview directly at the venue. Candidates who prefer to apply in advance may share their updated resume via email:
Candidates are advised to mention “Regulatory Affairs – ROW / EU” in the email subject line.
SEO-Optimized Job Title Variations
- Swiss Parenterals Regulatory Affairs Jobs in Ahmedabad
- B.Pharm M.Pharm Regulatory Affairs Careers – Swiss Parenterals
- Parenteral Regulatory Affairs Officer Jobs – EU & ROW Markets
- Injectable Regulatory Affairs Openings at Swiss Parenterals
Why Build Your Career with Swiss Parenterals
Working at Swiss Parenterals provides exposure to global regulatory frameworks governing sterile injectable products. Regulatory professionals in this role directly contribute to faster approvals, compliance assurance, and global availability of life-saving parenteral medicines, making a tangible impact on healthcare outcomes.
FAQs
Who can attend this walk-in interview?
Candidates with B.Pharm or M.Pharm qualifications and 2–4 years of regulatory affairs experience can attend.
Is parenteral experience mandatory?
Yes. Strong exposure to parenteral dosage forms is mandatory.
Which markets will this role handle?
ROW markets including Africa, CIS, ASEAN, LATAM, MENA, and the EU region.
Can I apply by email instead of attending the walk-in?
Yes. Candidates can share their resume via the provided email IDs.
What documents should I carry for the interview?
Updated resume, educational certificates, experience documents, and ID proof.
| Company | Swiss Parenterals Ltd. |
|---|---|
| Vacancies | Regulatory Affairs Officer, Regulatory Affairs Executive |
| Required Education | B.Pharm, M.Pharm |
| Experience | 2–4 years |
To apply for this job email your details to hroffice@swiss.in
