Senior Associate Specialist,Quality

I00M05 Wipro GE Healthcare Private Limited; Bengaluru; On-site; INR 2,000,000 - 4,000,000; Full time

Job summary

GE HealthCare seeks a senior quality assurance professional to drive compliance and quality culture across products and sites in Bengaluru. You will ensure regulatory alignment, implement QMS processes, and support cross-functional teams to meet medical device standards.

The role requires strong understanding of FDA 21 CFR 820, ISO 13485, IEC 62304, and related regulatory frameworks, with a focus on execution and collaboration within a global organization.

Qualifications

• Bachelor's degree from an accredited university or college.
• Minimum 5+ years of relevant experience.
• Strong oral and written communication skills.

Responsibilities

• Creates a quality culture by driving compliance activities related to a product, site, or region.
• Ensure quality and regulatory compliance while improving process effectiveness and efficiency.
• Understand Medical Device QMS requirements and regulatory standards (FDA, IEC 62304, ISO 13485).

Skills

Strong communication skills

Education

Bachelor's degree

Job description

Job Description Summary

Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. Ensures that projects and products are capable and will meet specified standards (Preventive). Impacts quality of own work and the work of others on the team. Focused on execution of standard enabling activities/provision of advice subject to policy and work routines within an enabling discipline. There may be some latitude to rearrange the sequence to complete task/duties based on changing situations. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. 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. 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.

Job Description Roles and Responsibilities

Creates a Quality culture by driving compliance activities around a specific product, site or region. This includes being responsible for the total quality management system for the business and driving Quality metrics. You will ensure quality and regulatory compliance while driving process effectiveness and efficiency. Broadening knowledge of theories, practices and procedures in own discipline to execute functional policy/strategy; still developing functional knowledge and skills. Basic understanding of key business drivers; uses this understanding to accomplish own work. Good understanding of how work of own team integrates with other teams and contributes to the area. May have some autonomy to make decisions within a defined framework. Resolves issues in situations that require good knowledge and judgment within established procedures. Consults more senior team members for issues outside of defined policy/parameters. A job at this level requires good interpersonal skills. Explains technical information to others. Candidate should have an awareness of Software Development Methodologies, Computer system validations. Knowledge of ISO 13485 standards , ISO 14971 standards, IEC 62304 and medical device regulations.

Required Qualifications

• Bachelor's degree from an accredited university or college


• Minimum 5+ Years of relevant experience.

Desired Characteristics

• Strong oral and written communication skills.


• Ability to document, plan, market, and execute programs.


• Demonstrated understanding of Medical Device QMS requirements and regulatory requirements including but not limited to FDA(Food and Drug Administration) 21 CFR( Code of Federal Regulations) 820, IEC (International Electrotechnical Commission) 62304-2006 (Medical Device Software), and ISO 13485.

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.

Additional Information

• Relocation Assistance Provided: No

At GE HealthCare, we see possibilities through innovation. We’re partnering with our customers to fulfill healthcare’s greatest potential through groundbreaking medical technology, intelligent devices, and care solutions. Better tools enabling better patient care. Together, we are not only building a healthier future but living our purpose to create a world where healthcare has no limits.