Drug Regulatory Affair Executive

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

Regulatory affairs professionals play a critical role in the drug development process, working closely with other stakeholders to ensure that pharmaceutical products meet regulatory requirements at every stage of development. Some of their key responsibilities include ( CTD/ ACTD DOSSIER PREPRATION ( MARKET ASEAN, CIS ROW ) **Regulatory Strategy...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

**JOB DISCRIPTION ( Drug regulatory affairs )** **1. Drug Regulatory Affairs - Job description** Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø Perform assessments of new or revised products Ø Manage complaint documentation (including investigation and Ø closure) Ø Respond to inquiries from regulatory bodies Ø Should be...

Job Description: - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market. - Review of technical...

Job Description: - CDSCO Registration for medical devices, Drug & Cosmetics as per the rules and standards. - Draft, review, submission and archival of other regulatory submissions (Query responses, corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for Indian market. - Review of technical...

JOB DESCRIPTION: - Ø Prepare CTD, ACTD Dossiers and file regulatory submissions Ø A Bachelor’s/ Master degree in B. Pharma / M. Pharma Ø Perform assessments of new or revised products Ø Experienced with 1 Yrs should apply. Ø Good Communication skills Job Type-Fulltime contact no-8810226562 **Salary**: ₹15,000.00 - ₹25,000.00 per...

We are seeking a skilled technical professional to fill this role. The ideal candidate will possess:Strong knowledge of pharmaceutical regulatory frameworks and data integrity standards.Excellent communication and interpersonal skills, with ability to facilitate workshops and collaborate with cross-functional teams.Proven experience in managing product...

Job Opportunity:This role leads the growth of our Regulatory Division.Responsibilities include developing and implementing regulatory strategies, delivering advisory and compliance services, and maintaining senior stakeholder relationships.Candidates should have 12+ years of experience, expertise in regulatory services, and credentials as a Company Secretary...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Expert to head our expanding Regulatory Division. As a senior leader, you will play a pivotal role in shaping the future of regulatory services and driving growth for our organization.