Azurity Pharmaceuticals job vacancy in Hyderabad
If you are looking for a leadership role in regulatory affairs within the pharmaceutical sector, this Azurity Pharmaceuticals job vacancy in Hyderabad could be an excellent opportunity. The company is actively hiring for the position of Manager, Regulatory Affairs, offering a strategic role in global regulatory submissions, life-cycle management, and compliance.
About Azurity Pharmaceuticals
Azurity Pharmaceuticals is a specialty pharmaceutical company focused on developing innovative dosage forms for underserved patient populations. It leverages its integrated commercial, scientific, and regulatory expertise to deliver high-quality medications across multiple therapeutic areas such as cardiovascular, endocrinology, neurology, and gastrointestinal care.
With a strong commitment to quality and patient-centric products, Azurity provides a professional environment that supports innovation, team collaboration, and meaningful career growth.
Job Summary – Manager, Regulatory Affairs
- Job Title: Manager, Regulatory Affairs
- Company: Azurity Pharmaceuticals
- Location: Hyderabad, Telangana, India
- Employment Type: Full-time
- Industry: Pharmaceutical / Regulatory Affairs
- Seniority Level: Mid-Senior / Manager
As Manager of Regulatory Affairs, you’ll play a crucial role in coordinating and executing regulatory strategies to support product registrations and ongoing compliance across markets.
Azurity Pharmaceuticals job vacancy in Hyderabad Key Responsibilities
In this role, you will be responsible for:
- Leading and managing regulatory filings such as MAAs, variations, and maintenance submissions
- Coordinating with regulatory agencies (e.g., EMA, NCA) and internal cross-functional teams
- Reviewing and preparing regulatory documentation
- Ensuring product labeling compliance with current regulatory guidelines
- Monitoring evolving regulatory requirements and advising on strategy
- Assisting in global regulatory life-cycle activities to secure and maintain approvals
This position is ideal for candidates with strong regulatory experience and strategic thinking skills in the pharmaceutical field.
Azurity Pharmaceuticals job vacancy in Hyderabad Required Skills & Qualifications
Successful applicants should possess:
- A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or a related discipline
- 5+ years of experience in regulatory affairs within the pharma industry
- Strong knowledge of European and international regulatory frameworks (e.g., EMA, MRP/DCP)
- Experience managing submissions and communication with regulatory bodies
- Excellent communication, documentation, and project management skills
Azurity Pharmaceuticals job vacancy in Hyderabad Job Location
📍 Hyderabad, Telangana, India – a major hub for pharmaceutical and biotechnology industries in India.
Why Join Azurity Pharmaceuticals?
Working in this managerial role at Azurity offers:
✨ A leadership position with strategic influence
✨ Exposure to international regulatory procedures and frameworks
✨ Collaboration with scientific, commercial, and quality assurance teams
✨ Career growth and development in a fast-growing pharma company
This role is perfect for experienced regulatory professionals who want to make a meaningful impact in product approvals and global health outcomes.
Azurity Pharmaceuticals job vacancy in Hyderabad How to Apply
- Update your resume to highlight relevant regulatory experience.
- Include key regulatory terms (e.g., EMA, MRP/DCP, submission strategies).
- Apply directly through CLICK HERE
- Prepare a strong cover letter emphasizing your regulatory leadership experience.
