Navatio Pharma is hiring Regulatory Affairs Specialist in Hyderabad 2025. Apply now for high-paying pharma regulatory jobs with 2-3 years experience. Work on USFDA, EMA, CDSCO submissions.
Navatio Pharma Hiring Regulatory Specialist in Hyderabad 2025 – Apply Now for High-Paying Pharma Regulatory Jobs
Are you a Regulatory Affairs professional looking to grow your career in one of India’s most rapidly expanding pharmaceutical companies? Navatio Pharma Solutions Private Limited is hiring talented individuals with 2–3 years of experience in pharmaceutical regulatory affairs to join their team in Hyderabad, India.
If you have strong expertise in CTD dossiers, DMFs, ANDAs, and global regulatory submission processes for authorities like USFDA, EMA, CDSCO, this is an excellent opportunity to build a high-paying and stable career in the booming Indian pharmaceutical regulatory sector.
🚨 Open Position: Regulatory Specialist
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Location: Hyderabad
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Employment Type: Full-Time
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Company: Navatio Pharma Solutions Private Limited
🔍 Required Qualifications:
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Educational Background:
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Bachelor’s or Master’s Degree in Pharmacy, Pharmaceutical Sciences, or Life Sciences
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Professional Experience:
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2 to 3 years of hands-on experience in regulatory affairs (pharmaceutical industry preferred)
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Skills Required:
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Excellent documentation and communication skills
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Strong knowledge of international regulatory frameworks: USFDA, CDSCO, EMA
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Experience with CTD (Common Technical Document) submissions
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Familiarity with Drug Master Files (DMFs), ANDAs, Variations, Renewals, and Post-Approval Changes
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Regulatory tracking system maintenance
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🔹 Key Responsibilities:
✅ Prepare and compile regulatory submissions including CTD dossiers, ANDAs, DMFs
✅ Ensure accurate and timely submissions to authorities like USFDA, CDSCO, EMA, MHRA
✅ Manage product lifecycle documentation: post-approval changes, variations, renewals
✅ Monitor and implement updates in global regulatory requirements
✅ Maintain regulatory approvals and registration databases
✅ Support regulatory audits and inspections with accurate documentation
✅ Maintain and update regulatory tracking systems ensuring data integrity
📩 How to Apply:
Interested candidates can apply by sending their updated resume to:
📧 hr@navatiopharma.com
🌟 Why Join Navatio Pharma?
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Work on international regulatory submissions for regulated markets (US, Europe, India, ROW)
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Exposure to complex filings like ANDA, DMF, NDA, MA submissions
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Hands-on experience with USFDA audits, EMA inspections, CDSCO filings
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Competitive salary and benefits in one of India’s fastest-growing pharma hubs — Hyderabad
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Build expertise in global regulatory compliance and documentation
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Long-term career stability with opportunities for international assignments.
Disclaimer:
This job posting is shared for informational purposes only. Please apply directly through the provided email for genuine job opportunities.
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