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    Job · 10900196

    Essilor logo

    QMS Lead & Market Quality Management

    Essilor · Kolkata · onsite · Posted 72d ago

    ₹7.0L - ₹12.0L PA8–12 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Job Title: QMS Lead & Market Quality Management

    Location: Bangalore, India

    If youve worn a pair of glasses, we’ve already met. We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in over 150 countries access to a global platform of high-quality vision care products and world-renowned brands.

    Join our global community of dedicated employees driving transformation in the eyewear and eyecare industry.

    Your Role

    Reporting to the Quality Leadership Team, you will lead and manage the Quality Management System (QMS) and Market Quality activities for ophthalmic lens manufacturing, edging, and mounting operations in India. You will ensure compliance with regulatory and quality standards while driving customer satisfaction and continuous improvement initiatives.

    Main Responsibilities

    Quality Management System (QMS)

    Own and implement the Quality Management System for ophthalmic lens manufacturing, edging, and mounting operations

    Ensure compliance with ISO 13485:2016 and CDSCO MDR 2017 requirements

    Establish, maintain, and continuously improve QMS processes for Class A ophthalmic devices

    Lead Management Reviews, Internal Audits, CAPA closures, and compliance monitoring

    Maintain audit calendars, compliance dashboards, SOPs, Work Instructions, Quality Manuals, and quality documentation

    Manage document control processes and ensure adherence to regulatory standards

    Market Quality Management

    Manage post-market surveillance activities, complaint investigations, and field quality feedback for ophthalmic lenses and mounted spectacles

    Monitor claims, returns, customer surveys, market feedback, and manufacturing quality trends

    Identify recurring issues and implement corrective and preventive actions (CAPA)

    Drive continuous improvement projects in collaboration with Operations, Technical, and Regional Quality teams

    Monitor new product launches post-release to ensure product quality and customer satisfaction

    Supplier Quality & Compliance

    Approve suppliers and vendors after quality audits

    Monitor supplier quality performance through ratings, non-conformance reports, and corrective actions

    Ensure supplier compliance with company quality and regulatory standards

    Stakeholder Management & Leadership

    Independently lead quality-related projects and act as a QMS subject matter expert

    Collaborate with cross-functional teams and senior leadership to resolve quality issues and drive improvements

    Support a culture of quality, compliance, and customer-centricity across the organization

    Candidate Profile

    Experience

    10+ years of experience in Quality Management within Medical Devices, Manufacturing, or related industries

    Proven experience in leading large-scale transformation and certification projects in multicultural environments

    Strong exposure to QMS implementation, audits, CAPA management, and regulatory compliance

    Experience in ophthalmic, healthcare, or medical device industries preferred

    Technical Expertise

    Strong knowledge of ISO 13485:2016 and CDSCO MDR 2017 regulations

    Expertise in Internal Audits, CAPA, Supplier Quality Management, and Post-Market Surveillance

    Strong analytical and problem-solving capabilities

    Experience in quality improvement and compliance monitoring systems

    Key Skills & Competencies

    Strong leadership and stakeholder management skills

    Customer-oriented mindset with focus on quality excellence

    Excellent communication and collaboration abilities

    Strong analytical thinking and decision-making skills

    Ability to independently facilitate meetings and drive projects

    High level of ownership and accountability

    Educational Qualification

    Bachelor’s or Master’s degree in Science or related field

    Languages

    Proficiency in English

    Knowledge of regional languages is an advantage

    What’s in it for you?

    Access to cutting-edge learning and development platforms

    Opportunity to work on global quality and transformation initiatives

    Exposure to international quality standards and best practices

    Career growth opportunities within a global organization

    Collaborative and inclusive work culture

    Recruiting Process

    Our recruitment process may vary. If you are shortlisted, our recruitment team will guide you through the next steps of the hiring process.

    Diversity & Inclusion Commitment

    We are committed to creating an inclusive environment for all employees. We celebrate diversity and provide equal opportunities to all employees regardless of race, gender, ethnicity, religion, disability, sexual orientation, or any other characteristic that makes each individual unique.






    Sourced from naukri

    Skills

    ISO 13485:2016 and CDSCO MDR 2017CAPAQMS

    About Essilor

    Essilor logo

    Essilor

    Medical Equipment

    878

    employees

    1849

    177 years old

    Charenton-le-Pont

    France

    ₹7L – ₹12L PA

    This role

    About

    Essilor Group provides solutions to correct, protect and prevent the visual health of the 7.2 billion people in the world.

    Industries

    Medical EquipmentConsumer goodsInternetManufacturing

    Employee ratings

    337 reviews

    4.0/ 5

    Culture

    3.8

    Career growth

    2.9

    Work-life

    3.8

    Employees rate it well for

    Salary38Work Environment33Work Life Balance31Senior Management29Career Growth26

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