Regcure Pharma Regulatory Affairs Jobs Freshers
- Regcure Pharma Hiring Regulatory Affairs Officer – Freshers Jobs in Ahmedabad (0–1 Year Experience)
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs Officer
- Eligibility / Qualifications
- Location & Salary
- Additional Benefits
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What is CTD/eCTD?
- What career growth can I expect?
- Is this a good career option?
- Summary
Regcure Pharma Hiring Regulatory Affairs Officer – Freshers Jobs in Ahmedabad (0–1 Year Experience)
Regcure Pharma is hiring Regulatory Affairs Officer roles in Ahmedabad for freshers and candidates with up to 1 year of experience. This is a full-time, on-site opportunity in regulatory affairs, ideal for candidates looking to build a career in dossier preparation, global submissions, and pharmaceutical compliance.
Multiple vacancies are expected for this entry-level regulatory role, making it a strong opportunity for M.Pharm graduates who want hands-on exposure to CTD/eCTD submissions and global regulatory frameworks.
Company Overview
Regcure Pharma is a regulatory-focused pharmaceutical services company specializing in compliance, dossier preparation, and global regulatory submissions. The company supports pharmaceutical organizations in meeting international standards across regulated markets.
With a strong focus on quality, documentation, and compliance, Regcure Pharma provides an ideal environment for early-career professionals to gain expertise in regulatory affairs and submission processes.
Job Role & Responsibilities
Regulatory Affairs Officer
- Assist in preparation and compilation of regulatory dossiers (CTD/eCTD)
- Support DMF documentation and regulatory submissions for global markets
- Ensure compliance with international regulatory guidelines
- Maintain accurate documentation and submission records
- Work with cross-functional teams for data collection and submission support
- Use MS Office tools for documentation, tracking, and reporting
Eligibility / Qualifications
- Educational Qualification: M.Pharm (Regulatory Affairs, Pharmaceutics, Pharmacology, QA)
- Experience: 0–1 year (freshers eligible)
- Strong knowledge of CTD/eCTD structure and global regulatory requirements
- Basic computer skills (MS Office)
- Good communication and documentation skills
Relevant Courses: M.Pharm Regulatory Affairs, M.Pharm Pharmaceutics, M.Pharm Pharmacology, M.Pharm Quality Assurance
Location & Salary
- Job Location: Ahmedabad, Gujarat, India
- Work Mode: On-site
- Salary Range: ₹2.5 LPA – ₹5 LPA (approximate for entry-level regulatory affairs roles)
Additional Benefits
- 2nd & 4th Saturday Off
- Professional growth in global regulatory domain
Application Process
Apply directly through the official form:
Apply Here: https://docs.google.com/forms/d/e/1FAIpQLSc2oghxl4tsv-ys4cqg1NHwwtyRGw7a0hsWJJMJIXWjWJL7_Q/viewform
Shortlisted candidates will be contacted for interview rounds.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes, this is an entry-level role suitable for freshers with M.Pharm.
What is CTD/eCTD?
CTD/eCTD is the standard format used for submitting regulatory documents to global health authorities.
What career growth can I expect?
You can grow into Regulatory Affairs Executive, Senior Regulatory Specialist, or Global Submission Lead.
Is this a good career option?
Yes, regulatory affairs is a high-demand and stable career in the pharmaceutical industry.
Summary
| Category | Details |
|---|---|
| Company | Regcure Pharma |
| Vacancies | Regulatory Affairs Officer |
| Required Education | M.Pharm (Regulatory Affairs, Pharmaceutics, Pharmacology, QA) |
| Experience | 0–1 year (freshers eligible) |
To apply for this job please visit docs.google.com.
