Looking for Regulatory Affairs Executive jobs in Satara? Nysa Biomed has announced a walk-in drive for Regulatory Affairs Executive/Officer positions for candidates with 0–5 years of experience. Candidates with B.Pharm or M.Pharm qualifications can attend the interview directly at the Satara location.
This pharmaceutical regulatory affairs job opportunity is ideal for freshers and experienced professionals seeking careers in dossier compilation, CTD/eCTD submissions, regulatory compliance, and pharmaceutical documentation.
Job Overview
| Particulars | Details |
|---|---|
| Company Name | Nysa Biomed |
| Job Role | Regulatory Affairs Executive/Officer |
| Job Location | Satara |
| Experience Required | 0–5 Years |
| Qualification | B.Pharm, M.Pharm |
| Employment Type | Full Time, Permanent |
| Industry | Pharmaceutical & Life Sciences |
| Walk-in Dates | 16 May 2026 – 31 May 2026 |
| Interview Timing | 10:30 AM – 5:30 PM |
| Openings | 5 |
Walk-in Venue Details
Venue:
Tulshi Vihar, Vishawa Naka, Satara – 415002
Contact Person:
Mahesh Pawar – 9145126373
Key Responsibilities
Candidates applying for this Regulatory Affairs Officer job in Satara will be responsible for:
- Preparation, review, and compilation of CTD/ACTD/eCTD dossiers
- Compilation of Modules 1 to 5 for product registration
- Review of stability data, specifications, STP, BMR/BPR documents
- Handling process validation documents and COA review
- Preparation and review of pack inserts, labels, and artworks
- Supporting submissions for ROW markets, semi-regulated markets, and domestic FDA submissions
- Assisting in product registration, renewals, variations, and re-registrations
- Coordinating with QA, QC, Production, R&D, Packaging, and Purchase departments
- Maintaining regulatory databases, trackers, archival systems, and version control
- Supporting responses for regulatory queries and deficiencies
Required Skills
Applicants should possess:
- Basic knowledge of pharmaceutical regulatory affairs
- Understanding of CTD/eCTD dossier structure
- Knowledge of GMP, CDSCO, WHO-GMP, and ICH guidelines
- Good documentation and coordination skills
- Ability to manage submission timelines and regulatory records
Educational Qualification
Required Qualification
- B.Pharm in any specialization
Preferred Qualification
- M.Pharm in Pharmacy
Why Join Nysa Biomed?
Working with Nysa Biomed offers candidates exposure to:
- Regulatory dossier preparation
- International and domestic submissions
- Pharmaceutical compliance systems
- Cross-functional pharmaceutical operations
- Career growth in Regulatory Affairs
Freshers looking for pharmaceutical regulatory affairs jobs in Maharashtra can gain practical exposure to CTD/eCTD compilation and submission processes.
How to Apply
Eligible candidates can directly attend the walk-in interview between 16 May 2026 and 31 May 2026 with:
- Updated Resume/CV
- Educational Certificates
- Experience Documents (if applicable)
- Passport-size Photographs
- Government ID Proof
Candidates are advised to reach the venue during the interview timing mentioned above.
TRY TO GO TMRW ONLY | NEARBY CANDIDATES ONLY | THEY HAVE MENTION FROM 16th to 31th But You Know How things Go in Walk in
