Job Description

Job Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072
Position Type: Full Time
Salary Range: ₹5.00 - ₹8.00 Salary/year
Job Shift: Day
Role Definition:
The  Research Associate(RA) Regulatory Affairs (RA) is responsible for the strategic and operational aspects of regulatory, review, compilation, submissions, approvals, and compliance across multiple markets (i.e. USA, EU, Canada etc. but not limited to these). This role ensures timely  submissions of quality applications ,approvals, robust regulatory knowledge,  and adherence to global regulatory standards. The SRA also supports cross-functional business objectives.
2. Key Responsibilities:
2.1 Regulatory Strategy & Dossier Management:
2.1.1 Should have prior 3-5  years submissions experience, including new product approvals, PLCM/Supplements/ variations, Annual reports/renewals, and amendments across Global markets with competent Global Regulatory Authorities (i.e. U.S. FDA, EMA, Health Canada etc.) for Complex Solid Oral Dosage forms and Injectables.
2.1.2 Ensure all submissions meet country-specific regulatory requirements and internal quality standards.
2.1.3 Support regulatory guidance to cross-functional teams (R&D, Quality, Project Management, Purchase Team, CMO, API Vendor etc.) for product lifecycle management.
2.1.4 Track and resolve regulatory authority deficiencies to avoid delays in approvals.
2.1.5 Maintain and monitor approval timelines to ensure regulatory compliance and business continuity.
2.2 Regulatory Intelligence & Compliance :
2.2.1 Monitor  and keep updated over the global regulatory changes and evolving regulatory  requirements/or expectations and provide strategic recommendations to ensure to remain in compliance.
2.4 Regulatory Data & Documentation Management:
2.4.1 Ensure that all regulatory documents, submissions, and correspondence are archived in time periodically  in an organized, traceable manner.
2.4.2 Maintain integrity, traceability, and accuracy of regulatory databases and electronic records of ANDA/MAA/DCP/MRP/CP/ANDS/IND etc, but not limited to these .
2.4.3 Collaborate with internal stakeholders/cross functional team to support strategy, compliance, and operational excellence.
Position:
Role:   Research Associate-Global Regulatory Affairs
Industry Type: Pharmaceutical
Education
PG: M.Pharm, in Pharmaceuitics /or Regulatory Affairs
Any additional degree is preferred.
Key Skills
Regulatory Affairs

Experience: Minimum 3-5 Years of Experience in regulatory affairs with OSD/Parenteral including conventional as well as complex dosage forms in generic space (ANDA/MAA/ANDS) and/or NDA/505(b)(2).
M.PharmEducation
PG: M.Pharm, in Pharmaceuitics /or Regulatory Affairs
Any additional degree is preferred.
Key Skills
Regulatory Affairs

Experience: Minimum 3-5 Years of Experience in regulatory affairs with OSD/Parenteral including conventional as well as complex dosage forms in generic space (ANDA/MAA/ANDS) and/or NDA/505(b)(2).