{"id":6725,"date":"2026-07-21T05:37:13","date_gmt":"2026-07-21T05:37:13","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=dr-reddys-regulatory-affairs-analyst-hiring-2026"},"modified":"2026-07-21T05:37:13","modified_gmt":"2026-07-21T05:37:13","slug":"dr-reddys-regulatory-affairs-analyst-hiring-2026","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=dr-reddys-regulatory-affairs-analyst-hiring-2026","title":{"rendered":"Dr. Reddy’s Regulatory Affairs Analyst Hiring 2026"},"content":{"rendered":"


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\"Dr.<\/a><\/div>\n

\n\u2714 Verified by Medical Jobs India<\/span>\n<\/p>\n

\nDr. Reddy’s Hiring Regulatory Affairs Analyst: Hyderabad IPDO
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\ud83c\udfe2 Dr. Reddy’s Laboratories<\/p>\n

\ud83d\udccd Hyderabad, Telangana<\/p>\n

\ud83c\udf93 M.Pharm, M.Sc (Pharmaceutical Sciences), PhD<\/p>\n

\ud83d\udcbc 4 to 8 Years Experience (Sterile Parenterals)<\/p>\n<\/div>\n

\nAre you seeking rewarding global dossier management opportunities via Dr. Reddy’s Careers Hyderabad<\/strong> or Regulatory Affairs Analyst Jobs<\/strong>? Multinational pharmaceutical leader Dr. Reddy’s Laboratories<\/strong> is inviting applications for the position of Regulatory Affairs Analyst at its Integrated Product Development Organization (IPDO) in Hyderabad.\n<\/p>\n

\nThis role requires 4 to 8 years of regulatory affairs experience, with specific exposure to US ANDA, 505(b)(2), EU, and Health Canada submissions for parenteral (sterile injectable) products. To structure a compliance-aligned resume that highlights your sterile dossier and eCTD expertise, read our guide on how to apply for healthcare and pharma jobs<\/a> online.\n<\/p>\n

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\ud83d\udccb Job Details<\/h3>\n
\n\n\n\n\n\n\n\n\n\n\n\n
Particular<\/th>\nDetails<\/th>\n<\/tr>\n
Company<\/td>\nDr. Reddy\u2019s Laboratories Ltd.<\/td>\n<\/tr>\n
Position<\/td>\nRegulatory Affairs Analyst \u2013 USA\/Canada\/EU<\/td>\n<\/tr>\n
Department<\/td>\nRegulatory Affairs General (IPDO)<\/td>\n<\/tr>\n
Job Location<\/td>\nHyderabad, Telangana, India<\/td>\n<\/tr>\n
Employment Type<\/td>\nFull-Time<\/td>\n<\/tr>\n
Experience Required<\/td>\n4 \u2013 8 Years in Regulatory Affairs (Sterile Parenterals)<\/td>\n<\/tr>\n
Qualifications<\/td>\nM.Pharm, M.Sc. (Pharmaceutical Sciences), PhD<\/td>\n<\/tr>\n
Estimated Salary<\/td>\n\u20b910,00,000 \u2013 \u20b918,00,000 per annum (CTC)<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<\/div>\n<\/div>\n
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\ud83d\udcbc Key Responsibilities<\/h3>\n