Looking to build a career in drug regulatory affairs and international business development? Neozen Healthcare is hiring a Regulatory Affairs & Business Development Executive in Ahmedabad. This opportunity is ideal for candidates with 1โ2 years of experience in CTD/ACTD dossier compilation, product registration, and pharma exports, especially those seeking growth in global regulatory markets like LATAM, MENA, and Africa.
With increasing demand for regulatory affairs professionals in pharmaceutical exports, this role combines technical regulatory expertise with client-facing business developmentโmaking it a high-growth hybrid career path.
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Job Overview
- Role: Regulatory Affairs & Business Development Executive
- Company: Neozen Healthcare LLP
- Location: Ahmedabad, Gujarat
- Experience: 1โ2 years
- Salary: โน2โ3 LPA (approx.)
- Employment Type: Full-Time, Permanent
- Industry: Pharmaceutical & Life Sciences
Key Responsibilities
Regulatory Affairs Functions
- Prepare and submit regulatory dossiers (CTD, ACTD, and country-specific formats)
- Manage product registration and renewals across global markets
- Handle regulatory queries and authority communications
- Review regulatory documents such as:
- SMPC
- COA
- FSC
- Stability data
- Validation protocols and reports
- Ensure compliance of product artwork, packaging, and promotional materials
Business Development Functions
- Identify and convert international pharma business leads
- Engage with clients across LATAM, CIS, MENA, Africa, and SEA regions
- Prepare quotations and manage client negotiations
- Build long-term relationships to drive pharmaceutical export growth
Cross-functional Coordination
- Collaborate with internal teams for regulatory submissions and product launches
- Maintain tracking systems for product registration status
Required Qualifications
- Education: B.Pharm / B.Sc (Life Sciences or related field)
- Experience: 1โ2 years in drug regulatory affairs or pharma exports
- Strong knowledge of:
- CTD & ACTD dossier compilation
- ICH guidelines
- International regulatory markets (LATAM, CIS, ROW)
- Skills:
- Excellent communication and negotiation
- Attention to detail and compliance mindset
- Basic proficiency in Excel and documentation tools
Preferred Candidate Profile
- Experience in pharmaceutical product registration
- Exposure to international business development in pharma
- Ability to work independently and handle multiple regulatory projects
- Positive attitude and willingness to learn
Benefits of This Role
- Exposure to global pharmaceutical regulatory markets
- Hands-on experience in dossier preparation and submission
- Opportunity to develop business development skills in pharma exports
- Career growth in regulatory affairs + international sales hybrid roles
How to Apply
