Regulatory Affairs Job in Hyderabad at Jodas Expoim. Apply via email for parenteral pharma role today.
Professionals with experience in global regulatory affairs now have an excellent career opportunity in the pharmaceutical sector. A well-established pharma organization is hiring skilled candidates for Regulatory Affairs roles focused on ROW (Rest of World) markets. This position is best suited for individuals with hands-on expertise in dossier preparation and regulatory submissions, especially for parenteral formulations.
Company Overview
Jodas Expoim is a reputed pharmaceutical organization known for its strong presence in international markets. The company specializes in developing and manufacturing high-quality formulations, including injectables, and has built a solid reputation for regulatory compliance and innovation. With a focus on expanding global reach, it offers professionals the opportunity to work on diverse regulatory projects across multiple countries.
Job Overview (Job Details)
| Category | Details |
|---|---|
| Organization | Jodas Expoim |
| Role | Regulatory Affairs – ROW Market (Parenterals) |
| Qualification | Bachelor’s / Master’s in Pharmacy or Life Sciences |
| Experience | 4–7 Years |
| Job Location | Hyderabad |
| Employment Type | Full-Time |
| Application Mode | |
| Salary | ₹6,00,000 – ₹12,00,000 per annum (Approx.) |
Job Location & Employment Type
The position is based in Hyderabad, a major hub for pharmaceutical and life sciences industries in India. This is a full-time role offering long-term career growth and stability.
Open Positions / Department Details
The company is hiring experienced professionals within the Regulatory Affairs department, specifically focusing on ROW markets. The role primarily involves working on injectable (parenteral) product dossiers and managing international regulatory submissions.
Key Roles & Responsibilities
Selected candidates will play a critical role in managing regulatory processes for global markets. Responsibilities include:
- Preparation and review of regulatory dossiers for various ROW countries
- Handling complete submission lifecycle, including compilation and dispatch
- Development of CTD Modules 2, 3, 4, and 5 as per regulatory requirements
- Ensuring compliance with country-specific guidelines and regulatory frameworks
- Coordinating with internal departments such as R&D, QA, and manufacturing
- Monitoring submission timelines and maintaining regular follow-ups with regulatory authorities
- Maintaining accurate regulatory documentation and records
- Supporting responses to regulatory queries and deficiency letters
This role requires a high level of accuracy, regulatory knowledge, and the ability to manage multiple submissions simultaneously.
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related discipline
Experience
- 4–7 years of relevant experience in Regulatory Affairs
- Hands-on experience working with ROW markets
Skills Required
- Strong expertise in CTD Modules 2–5 preparation
- Experience in handling parenteral (injectable) products (mandatory)
- In-depth understanding of global regulatory guidelines
- Ability to manage end-to-end submission processes independently
- Strong coordination and communication skills
- Detail-oriented approach with strong documentation skills
Note: Candidates with only publishing experience and no hands-on regulatory exposure will not be considered.
Salary & Benefits
- Estimated salary: ₹6 LPA – ₹12 LPA (depending on experience)
- Opportunity to work on international regulatory submissions
- Exposure to multiple global markets and regulatory standards
- Career growth in a specialized and high-demand domain
- Professional work environment with cross-functional collaboration
Selection Process
The hiring process is expected to include:
- Resume Screening
- Technical Evaluation / Interview
- HR Discussion
- Final Selection
Candidates with relevant experience and immediate availability may have an advantage during the selection process.
How to Apply
Interested candidates can apply by sending their updated resume to:
Ensure your CV clearly highlights your regulatory experience, especially in ROW markets and parenteral products.
Important Dates
- Last Date to Apply: Not specified (early application recommended)
Why Apply for This Pharma Job?
This opportunity is ideal for regulatory professionals looking to expand their expertise in international markets. Working on ROW submissions allows candidates to gain exposure to diverse regulatory frameworks and strengthen their technical knowledge.
The role offers hands-on involvement in dossier preparation and submission processes, making it highly valuable for long-term career growth. Additionally, working with a reputed pharmaceutical company enhances professional credibility and opens doors to advanced global opportunities.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any recruiter or company. Applicants are advised to verify all details independently before applying. No charges are applicable for job applications shared on this platform.
Final Call-to-Action
If you have experience in regulatory affairs and want to work on global pharmaceutical submissions, this is the right opportunity. Apply now with your updated resume and take the next step in advancing your career in regulatory affairs.
