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Senior Regulatory Affairs Specialist

Philips
10+ years
Not Disclosed
Pune, India
1 June 2, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Senior Regulatory Affairs Specialist

Location: Pune, India
Employment Type: Full-Time
Department: Regulatory Affairs – Sleep & Respiratory Care (SRC)
Experience Required: 10+ Years
Work Model: Hybrid (Minimum 3 Days Office Presence per Week)

Position Overview

We are seeking an experienced Senior Regulatory Affairs Specialist to support regulatory strategy, product registrations, and compliance activities for the Sleep & Respiratory Care (SRC) portfolio. This role will focus on home and hospital respiratory care products, including ventilators, oxygen concentrators, respiratory devices, and associated accessories.

The successful candidate will lead global regulatory submissions, support product development initiatives, ensure compliance with international regulations, and collaborate with cross-functional teams to bring innovative medical devices to market while maintaining regulatory compliance throughout the product lifecycle.

Key Responsibilities

Regulatory Strategy & Product Lifecycle Management

  • Develop and execute regulatory strategies for:

    • New Product Development (NPD)

    • Design Changes

    • Product Enhancements

    • Field Safety Corrective Actions (FSCA)

    • Sustaining Engineering Activities

  • Provide regulatory guidance throughout the product lifecycle to ensure compliance with global regulations.

  • Assess regulatory impact of product modifications, labeling updates, and manufacturing changes.

Regulatory Submissions & Global Registrations

  • Lead preparation, review, and submission of:

    • FDA 510(k) Premarket Notifications

    • EU MDR Technical Documentation

    • Health Canada Medical Device License Applications

    • Global Product Registrations and Market Authorizations

  • Coordinate interactions with regulatory authorities, notified bodies, and competent authorities during submission reviews and approvals.

  • Support registration activities across the United States, European Union, Canada, and Rest of World (RoW) markets.

Cross-Functional Collaboration

  • Partner with:

    • Research & Development (R&D)

    • Design Quality

    • Manufacturing

    • Supply Chain

    • Marketing

    • Clinical Affairs

    • Quality Assurance

  • Provide regulatory input during product development, risk assessments, verification, and validation activities.

  • Ensure regulatory requirements are integrated into project plans and development processes.

Regulatory Compliance & Intelligence

  • Monitor evolving global regulatory requirements and industry standards.

  • Support implementation of new regulations, guidance documents, and standards.

  • Maintain compliance with:

    • FDA 21 CFR Part 820

    • EU MDR (Regulation (EU) 2017/745)

    • ISO 13485

    • Applicable international regulatory standards

  • Conduct regulatory assessments to support product launch and post-market activities.

Quality & Continuous Improvement

  • Support Quality Management System (QMS) compliance initiatives.

  • Identify opportunities for process improvement within regulatory operations.

  • Contribute to KPI monitoring, reporting, and compliance metrics.

  • Assist during internal audits, regulatory inspections, and compliance reviews.

Required Qualifications

Education

  • Bachelor's or Master's Degree in:

    • Biomedical Engineering

    • Health Sciences

    • Pharmaceutical Sciences

    • Life Sciences

    • Business Administration

    • Regulatory Affairs

    • Law or related discipline

Experience

  • Minimum 10+ years of experience in:

    • Regulatory Affairs

    • Quality Compliance

    • Product Development

    • Medical Device Industry

  • Proven experience supporting global regulatory submissions and product registrations.