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Senior Regulatory Affairs Manager

7 years
Not Disclosed
10 Sept. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Regulatory Affairs Specialist


Main Purpose of Role

The Regulatory Affairs Specialist is an experienced individual contributor with comprehensive expertise in regulatory affairs. The role involves executing highly complex or specialized projects, adapting precedents, and developing innovative solutions beyond traditional approaches to ensure compliance and successful regulatory outcomes.


Key Responsibilities

  • Act as a subject matter expert in Regulatory Affairs, leading the development and submission of product registration dossiers, progress reports, supplements, amendments, and periodic experience reports.

  • Serve as the primary regulatory liaison with health authorities to expedite approval processes for pending registrations.

  • Provide regulatory support throughout the product lifecycle, including development, approval, and post-marketing phases.

  • Contribute to product planning, regulatory strategy, risk management, and chemistry manufacturing control (CMC) activities.

  • Ensure timely approval of new drugs, biologics, or medical devices, as well as maintenance of continued approvals for marketed products.

  • Collaborate with marketing, research, and cross-functional teams as the regulatory representative.

  • Advise development and marketing teams on regulatory requirements related to manufacturing changes, line extensions, technical labeling, and interpretation of applicable regulations.


Qualifications

Education

  • Associate’s Degree (or equivalent, ~13 years of education) in a relevant field required.

Experience

  • Minimum of 7 years of progressive experience in Regulatory Affairs, with demonstrated expertise in product registrations, regulatory strategy, and health authority interactions.