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Regulatory Affairs Specialist

PLG groups
7-8 years
₹18–28 LPA
Remote, India, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Regulatory Affairs Specialist

Location: India
Work Mode: Remote (Possible)
Department: Life Cycle – Regulatory Affairs & Operations
Employment Type: Permanent

Experience: 7–8 years of experience in EU Regulatory Affairs, including regulatory submissions, lifecycle management, and project management.
Salary Package: ₹18–28 LPA (Approx., based on current market standards; final compensation depends on candidate experience and skills.)


Role Overview

The Regulatory Affairs Specialist is responsible for ensuring efficient execution of regulatory projects, delivering high-quality outcomes, and working with minimal supervision. This role supports regulatory activities throughout the product lifecycle, including pre-licensing, new registrations, post-licensing submissions, and regulatory compliance for client portfolios.


Key Responsibilities

Regulatory Operations

  • Contribute to regulatory activities performed on the Regulatory Affairs (RA) Platform/Hub.

  • Support pre-licensing activities, new site and medicinal product registrations, and post-licensing regulatory submissions.

  • Interact with health authorities on behalf of clients.

  • Prepare and maintain client administrative documents and reports for regulatory submissions.

  • Support initial Marketing Authorization (MA) applications and all Lifecycle Management (LCM) activities.

  • Compile or supervise the compilation of regulatory dossiers in accordance with national requirements.

Client & Stakeholder Management

  • Act as the Single Point of Contact (SPOC) for assigned client portfolios.

  • Coordinate and communicate with clients, external vendors, and cross-functional teams.

  • Participate in client meetings and prepare Minutes of Meeting (MoM).

  • Provide ongoing regulatory support to clients and affiliate organizations.

  • Liaise with sponsor headquarters, affiliate departments, and regulatory authorities on regulatory matters.

Regulatory Compliance

  • Track and document regulatory submissions and health authority approvals.

  • Monitor regulatory changes and communicate their impact to clients.

  • Obtain regulatory authority approvals for client submissions.

  • Review packaging texts, Summary of Product Characteristics (SmPC), Patient Information Leaflets (PIL), and labeling content for compliance.

Project Management & Team Support

  • Lead regulatory project activities and ensure project objectives are met.

  • Support, mentor, and review the work of Regulatory Affairs Associates.

  • Collaborate with project teams to identify and address regulatory requirements throughout project execution.

Systems & Documentation

  • Maintain regulatory tracking systems and databases.

  • Ensure accurate data entry into PLG tools for KPI and performance metric reporting.

  • Verify that invoicing is accurate and completed correctly.

Pre-Sales Support

  • Provide technical support during pre-sales activities.

  • Assist in preparing technical content for proposals.

  • Support quotation evaluations from a regulatory perspective.


Educational Qualification

  • Bachelor's degree or higher in a Science-related field or equivalent relevant experience.


Required Experience

  • 7–8 years of experience in EU Regulatory Affairs, including technical regulatory activities and project management.


Language Requirements

  • Excellent written English with strong grammar skills.

  • Good verbal communication skills in English.

  • Additional language proficiency is an advantage.


Technical Skills

  • Proficiency in Microsoft Word, Excel, and PowerPoint.

  • Good understanding of regulatory tracking databases and regulatory management software.

  • Ability to quickly learn and adapt to new software applications.


Key Competencies

  • Strong organizational and planning skills.

  • Excellent interpersonal and communication skills.

  • Effective cross-functional coordination abilities.

  • Strong project management capabilities.

  • Attention to detail and commitment to regulatory compliance.

  • Ability to mentor and support junior team members.

  • Ability to work independently as well as collaboratively within a team.

  • Client-focused approach with strong stakeholder management skills.

  • Excellent analytical and problem-solving skills.