DRA Manager Jobs in AXA Parenterals Ltd - Roorkee, Uttarakhand
10 - 15 Years of Experience
Not disclosed 
Full TimeAXA Parenterals Ltd.
Roorkee, Uttarakhand, India
Posted on 23-04-2026
1 Vacancy
Description
- Job Title: DRA Manager
- Qualification: BPharm
- Location: AXA Parenterals Ltd - Roorkee, Uttarakhand
- Work Experience: 10 to 15 Years
Job Description
- Prepare, review, and submit regulatory documents to local and international health authorities.
- Ensure compliance with national and international regulatory guidelines (FDA, EMA, CDSCO, etc.).
- Maintain up-to-date knowledge of regulatory requirements for pharmaceuticals, devices, or biotech products.
- Coordinate with R&D, QA, and Production teams to gather required data for submissions.
- Track submission timelines and ensure timely approvals for product registrations.
- Review and approve product labeling, packaging, and promotional materials from a regulatory perspective.
- Respond to regulatory queries and inspections from authorities.
Take this opportunity to join AXA Parenterals Ltd - Roorkee, Uttarakhand as a DRA Manager in Roorkee, Uttarakhand and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Functional Area
Regulatory Affairs / Pharmacovigilance
Preferred Education
Key Skills
About Organization
AXA Parenterals Ltd is a pharmaceutical manufacturing organization engaged in the production of sterile parenteral preparations, intravenous fluids, and life-saving medicines with a strong focus on product quality, regulatory compliance, and advanced manufacturing technology. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry standards. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring compliance with safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and operational efficiency.
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