Apply for high-paying Regulatory Affairs jobs at Axxelent Pharma Science in Chennai. Multiple vacancies open for Executive, Senior Executive, Assistant Manager, Deputy Manager & Manager positions in Formulations. Excellent career growth for pharma professionals.
Axxelent Pharma Science Hiring for Regulatory Affairs Roles – Executive to Manager Openings in Chennai 2025
Axxelent Pharma Science Private Limited, a leading formulation CDMO (Contract Development and Manufacturing Organization), is inviting dynamic and experienced professionals to join its Regulatory Affairs team at its state-of-the-art facility located at IIT M Research Park, Taramani, Chennai. If you’re looking for high-paying pharma jobs in India with strong growth potential and exposure to global regulatory frameworks, this is an outstanding opportunity.
With a strong presence in regulated markets like the US, Europe, Canada, and UK, Axxelent Pharma offers its employees unparalleled exposure to global dossier submissions, eCTD preparation, and post-approval regulatory lifecycle management — making it one of the best companies for Regulatory Affairs jobs in India 2025.
🌍 Why Join Axxelent Pharma Science?
Axxelent Pharma Science stands out in the pharmaceutical formulations CDMO sector for its:
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USFDA, EMA, Health Canada compliance
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Strong leadership in global regulatory submissions
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Comprehensive exposure to regulated markets worldwide
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Collaborative, innovation-driven culture
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High-growth career paths for pharma regulatory professionals
With Regulatory Affairs jobs in formulations becoming increasingly specialized and high-paying, working at Axxelent Pharma Science positions you at the forefront of the industry.
📢 Open Positions – Regulatory Affairs (Formulations)
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Executive
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Senior Executive
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Assistant Manager
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Deputy Manager
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Manager
Total Vacancies: 12 Positions
Department:
Regulatory Affairs (Formulations only)
Formulation CDMO R&D
🔬 Key Skills & Expertise Required
Candidates must demonstrate expertise in:
✅ Dossier preparation and submission for regulatory bodies like US FDA, EMA, Health Canada.
✅ Comprehensive understanding of US, EU, Canada, UK, ICH guidelines and global regulatory frameworks.
✅ Proficiency in eCTD (electronic Common Technical Document) structure and GMP compliance.
✅ Experience managing post-approval regulatory activities such as renewals, variations, amendments, and change control.
✅ Strong regulatory intelligence for global pharmaceutical markets.
✅ In-depth knowledge of multiple dosage forms and complex formulations.
✅ Excellent communication skills to interface with global regulatory authorities and internal teams.
🎓 Educational Qualifications
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B. Pharm / M. Pharm
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B. Tech / M. Tech (Pharma / Biotech)
Only candidates with a formulations background will be considered for these roles.
💼 Experience Required
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2 to 12 years of relevant experience in Regulatory Affairs (Formulations Only)
📍 Job Location
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IIT M Research Park, Taramani, Chennai, Tamil Nadu
This location provides an excellent environment for pharmaceutical research, regulatory operations, and professional development.
🏆 Why Regulatory Affairs Roles Are in High Demand?
With increasing globalization of drug development, regulatory affairs professionals play a critical role in ensuring timely and compliant market access for pharmaceutical products. Companies like Axxelent Pharma Science are continuously expanding their regulatory submissions for multiple regions:
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United States (US FDA)
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Europe (EMA, EU GMP)
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Canada (Health Canada)
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United Kingdom (MHRA)
Professionals with expertise in eCTD publishing, regulatory documentation, and compliance frameworks are among the most sought-after in the industry, offering high salaries, strong job security, and excellent global career prospects.
📩 How to Apply
Interested and eligible candidates can apply via:
Email:
WhatsApp Contact:
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📱 9789098123
Company Website:
If you’re seeking high-paying Regulatory Affairs jobs in India 2025, Axxelent Pharma Science offers one of the best platforms to accelerate your career in formulations regulatory submissions. With multiple vacancies across various levels, this is a rare opportunity to join a globally recognized CDMO that’s actively expanding its regulatory portfolio across international markets.
✅ Don’t miss this chance to work with a leading USFDA-approved pharmaceutical CDMO. Submit your resume today and unlock your global regulatory career.
