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Senior Lead Specialist Quality

Ge Healthcare
GE HealthCare
6 years
Not Disclosed
Bengaluru, Karnataka, India
10 Feb. 18, 2026
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

Senior Lead Specialist, Quality

Company: GE Healthcare
Location: Bengaluru, Karnataka, India
Job Type: Full Time
Experience Required: Minimum 6 years in Quality Assurance / Healthcare Quality within regulated industries
Job ID: R4036035

Role Overview

GE Healthcare is seeking a Senior Lead Specialist in Quality to develop, maintain, and execute quality systems, rules, and processes that ensure compliance with internal standards and global regulatory requirements. This role focuses on driving quality excellence across product lines, supporting Design Control Quality Management System compliance for both hardware and software medical devices. The Senior Lead Specialist ensures that all projects and new product introductions (NPI) meet customer expectations, regulatory standards, and organizational quality objectives.

Key Responsibilities

  • Lead quality initiatives and compliance activities for assigned products, sites, or regions, fostering a culture of quality excellence.

  • Ensure adherence to regulatory standards, including ISO 13485, FDA 21 CFR 820, IEC 62304, EU MDR/EUMDD, and internal Quality Management System (QMS) procedures.

  • Collaborate closely with product engineering teams to ensure Design Control compliance for new products and in-build deliverables.

  • Execute quality objectives, monitor metrics, and report outcomes to management and external agencies as required.

  • Utilize technical expertise and analytical skills to resolve complex quality issues and provide guidance within the team.

  • Provide mentorship and guidance to junior colleagues, sharing best practices in compliance, process execution, and quality documentation.

  • Contribute to process improvement initiatives, standard operating procedures (SOPs), and project documentation.

  • Leverage professional judgment to make decisions in alignment with established quality standards and policies.

Required Qualifications and Experience

  • Bachelor’s degree in Engineering, Pharmacy, or related discipline from an accredited institution.

  • Minimum 6 years of experience in Quality Assurance or Healthcare Quality in a regulated environment.

  • Strong knowledge of medical device QMS, Design Control, and compliance with regulatory standards (ISO 13485, FDA 21 CFR 820, IEC 62304, EU MDR/EUMDD).

  • Proven ability to analyze and resolve quality issues with technical expertise and problem-solving skills.

  • Strong communication, documentation, and interpersonal skills to effectively collaborate across teams.

Preferred Skills

  • Experience in leading quality initiatives for medical devices in both software and hardware domains.

  • Established project management capabilities and ability to drive quality objectives in a cross-functional environment.

  • Familiarity with audits, regulatory inspections, and continuous improvement processes.

Inclusion and Diversity

GE Healthcare is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or other legally protected characteristics. Employees are expected to act with humility, integrity, transparency, and ownership, contributing to a culture of collaboration and high performance.

Why GE Healthcare

Joining GE Healthcare offers the opportunity to work in a global, innovative environment, contributing to high-quality healthcare solutions. The role provides exposure to cross-functional teams, career growth, and engagement in projects that impact patient safety and product excellence worldwide.

Additional Information

Relocation Assistance: Not Provided