Talent.com
Lead Specialist, Regulatory Affairs - WHXR

Lead Specialist, Regulatory Affairs - WHXR

ConfidentialBengaluru / Bangalore, India
5 days ago
Job description

Job Description Summary

Join GE HealthCare as a Lead Specialist in Regulatory Affairs and play a pivotal role in shaping the future of medical imaging. This global leadership position offers the opportunity to drive regulatory strategies and lead cross-functional teams to bring innovative X-ray imaging products to market. Be part of a dynamic environment where your expertise will directly impact patient care and healthcare outcomes worldwide.

GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

Job Description

Key Responsibilities

  • Lead global regulatory projects to secure market authorization and promotional approval for medical devices.
  • Collaborate closely with product development teams, including engineering, marketing, clinical investigations, and regional regulatory experts.
  • Develop and implement regulatory strategies aligned with business objectives, including target markets, clinical claims, and timelines.
  • Identify and define product testing and clinical study requirements to support regulatory submissions.
  • Analyze and organize scientific data to demonstrate the safety and efficacy of medical devices.
  • Prepare and submit regulatory documentation to authorities across global markets including the US, Canada, Latin America, Europe, China, and Asia.
  • Provide regulatory guidance throughout the product development lifecycle to ensure compliance with international standards.
  • Evaluate design changes and determine licensing or registration needs.
  • Review and approve promotional materials to ensure alignment with regulatory claims.
  • Monitor regulatory trends and communicate new requirements to internal teams.
  • Support regulatory inspections and audits as needed.

Required Qualifications

  • Advanced experience in Regulatory Affairs, ideally within the medical device industry, or advanced experience in product development within the medical device industry.
  • Bachelor's degree from an accredited university or college, or equivalent relevant experience.
  • Strong analytical, problem-solving, and project management skills.
  • Excellent oral and written communication abilities.
  • Proficiency in English (written and spoken).
  • Preferred Qualifications

  • Experience interacting with global regulatory agencies (e.g., FDA, Notified Bodies, NMPA).
  • Knowledge of Quality Management Systems (QMS) and regulatory compliance frameworks.
  • Proven ability to work independently in a fast-paced, dynamic environment.
  • Adaptability to change and capability to drive positive transformation.
  • Excellent team orientation and responsiveness to customer needs.
  • Detail-oriented with a focus on delivering results.
  • Experience working in multicultural and cross-functional teams.
  • Inclusion and Diversity

    GE Healthcare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

    We expect all employees to live and breathe our behaviors : to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

    Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

    #Hybrid

    Additional Information

    Relocation Assistance Provided : No

    Skills Required

    Product Development, Project Management, Regulatory Affairs, regulatory documentation

    Create a job alert for this search

    Regulatory Specialist • Bengaluru / Bangalore, India

    Related jobs
    • Promoted
    Regulatory Affairs Specialist-API

    Regulatory Affairs Specialist-API

    BioconBengaluru, Karnataka, India
    Role Summary / Key Responsibilities.DMF compilation and submission to global markets.Handling post approval submission and CIP assessments. Submission of DMF amendment & response to Health Authority ...Show moreLast updated: 15 days ago
    • Promoted
    Regulatory Affairs Specialist - Peptides Or Injectable

    Regulatory Affairs Specialist - Peptides Or Injectable

    BioconBengaluru, Republic Of India, IN
    Formulation Regulatory Affairs - for Peptide products or Injectables.Level - Deputy Manager / Associate Manager.Formulation Regulatory Affairs for Peptide products or Injectables.Drafting controlled...Show moreLast updated: 13 days ago
    • Promoted
    Regulatory Affairs Manager- Sme

    Regulatory Affairs Manager- Sme

    Mount Talent Consulting Pvt Ltd.Bengaluru, Republic Of India, IN
    Domain lead - SME - Safety and Regulatory.Expert in Pharma domain’s multiple functions especially Regulatory and Safety.Well versed with business functions and tools used by industry.Able to create...Show moreLast updated: 22 days ago
    • Promoted
    Associate Staff Regulatory Affairs Specialist

    Associate Staff Regulatory Affairs Specialist

    ConfidentialBengaluru / Bangalore, India
    This position independently supports projects to bring new and modified medical devices to market and ensure ongoing compliance. This position participates on cross-functional teams, leads the devel...Show moreLast updated: 30+ days ago
    • Promoted
    Manager Global Regulatory Affairs

    Manager Global Regulatory Affairs

    ConfidentialBengaluru / Bangalore, India
    Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products including technical and Regulatory aspects.Developme...Show moreLast updated: 5 days ago
    • Promoted
    Regulatory Affairs Specialist - Peptides or Injectable

    Regulatory Affairs Specialist - Peptides or Injectable

    BioconBengaluru, Karnataka, India
    Formulation Regulatory Affairs - for Peptide products or Injectables.Level - Deputy Manager / Associate Manager.Formulation Regulatory Affairs for Peptide products or Injectables.Drafting controlled...Show moreLast updated: 14 days ago
    • Promoted
    Team Lead - Regulatory Reporting

    Team Lead - Regulatory Reporting

    ConfidentialBengaluru / Bangalore, India
    The Regulatory Reporting Centre of Excellence Team (RRCOE) within State Street Investment Management's Operations department is committed to delivering expert operational services through collabora...Show moreLast updated: 5 days ago
    • Promoted
    Regulatory Reporting Specialist

    Regulatory Reporting Specialist

    ConfidentialBengaluru / Bangalore, India
    Morgan Wealth Management is a global leader in investment and wealth management, serving institutions, high-net-worth individuals, and retail investors worldwide. As a Transaction Processing Special...Show moreLast updated: 5 days ago
    • Promoted
    Senior Regulatory Specialist

    Senior Regulatory Specialist

    ConfidentialBengaluru / Bangalore, India
    Warsaw, Bengaluru Luxor North Tower, Cairo Boomerang, Poznan Grunwaldzka.Are you looking for an opportunity to work on global projects and make a meaningful impact in the pharmaceutical industry.Jo...Show moreLast updated: 5 days ago
    • Promoted
    Senior Regulatory Affairs Specialist

    Senior Regulatory Affairs Specialist

    ConfidentialBengaluru / Bangalore, India
    We are seeking a detail-oriented and proactive Regulatory Affairs Associate to join our Global Regulatory team.In this role, you will be responsible for development and execution of CMC regulatory ...Show moreLast updated: 5 days ago
    • Promoted
    Senior Regulatory Compliance Specialist

    Senior Regulatory Compliance Specialist

    ConfidentialBengaluru / Bangalore, India
    Regulatory Compliance Specialist is a key position in the Regulatory Compliance export organization.This position drives the daily compliance activities required under the company's trade complianc...Show moreLast updated: 5 days ago
    • Promoted
    Regulatory Affairs Specialist - Peptides or Injectable

    Regulatory Affairs Specialist - Peptides or Injectable

    ConfidentialBengaluru / Bangalore, India
    Formulation Regulatory Affairs - for Peptide products or Injectables.Level - Deputy Manager / Associate Manager.Formulation Regulatory Affairs for Peptide products or Injectables.Drafting controlled...Show moreLast updated: 5 days ago
    • Promoted
    Regulatory Affairs Manager- SME

    Regulatory Affairs Manager- SME

    Mount Talent Consulting Pvt Ltd.Bengaluru, Karnataka, India
    Domain lead - SME - Safety and Regulatory.Expert in Pharma domain’s multiple functions especially Regulatory and Safety.Well versed with business functions and tools used by industry.Able to create...Show moreLast updated: 22 days ago
    • Promoted
    • New!
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    Dr. Reddy's Laboratoriesvijayapura, India
    We are seeking a detail-oriented Specialist in Regulatory Affairs primarily focusing on Oligonucleotides typically has a role that involves ensuring compliance with regulatory requirements for thes...Show moreLast updated: 20 hours ago
    • Promoted
    Regulatory Affairs Specialist

    Regulatory Affairs Specialist

    ConfidentialBengaluru / Bangalore, India
    Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products including technical and Regulatory aspects.Developme...Show moreLast updated: 30+ days ago
    • Promoted
    Regulatory Affairs (Executive), Plant Health

    Regulatory Affairs (Executive), Plant Health

    Sea6 Energy Pvt Ltd.Bengaluru, Karnataka, India
    At Sea6 Energy we envision a future where we can harness the potential of the oceans – to provide sustainable solutions in energy, agriculture and food. To accomplish this, a multidisciplinary team ...Show moreLast updated: 11 days ago
    • Promoted
    Regulatory Affairs Specialist-Api

    Regulatory Affairs Specialist-Api

    BioconBengaluru, Republic Of India, IN
    Role Summary / Key Responsibilities.DMF compilation and submission to global markets.Handling post approval submission and CIP assessments. Submission of DMF amendment & response to Health Authority ...Show moreLast updated: 15 days ago
    CTA / IND Regulatory Specialist

    CTA / IND Regulatory Specialist

    ScaleneWorksBengaluru, Karnataka, India
    Quick Apply
    Coordination of CTA submissions, to ensure timely delivery and ensuring the content is appropriate to each individual regulatory agency while maintaining compliance with Organization policy and pro...Show moreLast updated: 30+ days ago