Director Quality Regulatory Affairs

1 month ago


Delhi, India Qure.ai Full time
About Qure.AI:
Qure.AI is the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted over 22 million patients in more than 90 countries worldwide. At Qure.ai, we are committed to fostering a diverse and inclusive workplace where talent thrives.
About the Job
Job Title: Director – Quality & Regulatory Affairs
Job Description:
The Director of Quality & Regulatory Affairs will serve as the primary liaison for quality system management and regulatory affairs, interfacing with external (regulatory agencies, customers) and internal stakeholders. This role is ideal for someone with deep knowledge of AI regulations, Software as a Medical Device (SaMD), and global regulatory frameworks, especially FDA, EU MDR, cybersecurity, and quality standards. This individual will lead a team of specialists, coordinate cross-functional deliverables, and guide product approvals and compliance across global markets.
Roles and Responsibilities:
Regulatory Affairs & Compliance Leadership:
Act as the main regulatory liaison with global regulatory agencies for pre-submissions, submissions, and post-market activities.
Lead and oversee the development of regulatory pathways, including clinical study design and regulator negotiations.
Remain current with evolving regulations (FDA, EU MDR, ISO 13485, IEC 62304, ISO 14971) and advise on strategic implications.
Quality Management System (QMS) Oversight:
Ensure adherence to QMS policies and regulatory standards, including ISO 13485 and FDA guidelines.
Manage internal and external audits, including preparation, resolution of findings, and coordination with auditing groups.
Oversee documentation for Corrective and Preventative Actions (CAPA) and ensure it is communicated with all stakeholders.
Cross-functional Collaboration & Strategy:
Coordinate cross-functional activities to support product development, approval, and strategic planning.
Partner with internal teams to execute regulatory strategies for global market entry and compliance.
Act as a regulatory affairs advisor, guiding research directions and influencing strategic decisions.
Product Validation & Compliance:
Develop and review validation documentation for SaMD and CAD devices to ensure regulatory compliance.
Review product labeling, marketing materials, and customer statements for compliance and make recommendations.
Regulatory Documentation & Monitoring:
Assist in the preparation and submission of 510(k) filings.
Conduct regulatory monitoring activities to identify and respond to new or revised requirements, performing regulatory gap analyses.
What Does Success Look Like:
Success in this role includes ensuring that our products meet or exceed regulatory compliance standards, that cross-functional teams are aligned with regulatory requirements throughout product lifecycles, and that regulatory pathways are efficiently navigated to support timely market entry and sustainable compliance.
Skills and Expertise:
Proven experience in a senior regulatory role within an AI medical device company.
Extensive knowledge of FDA and EU MDR requirements, QMS, and medical device regulations.
Master’s degree (technical discipline preferred); RAC certification is a plus.
Strategic thinking with the ability to align regulatory needs with portfolio opportunities.
Strong project management and multitasking skills in cross-functional environments.
Exceptional written and verbal communication skills for clear documentation, presentations, and team discussions.
Demonstrated commitment to quality and continuous improvement, with a proactive approach to regulatory challenges.
At Qure.ai:
You will be part of a rapidly growing organization, with an opportunity to work alongside the best minds in the industry. Competitive compensation and rewards, along with the chance to grow with a young company.
Inclusive Workspace:
Qure.ai Inclusive Workspace
By submitting your information and application, you confirm that you have read and agree to the Applicant PrivacyPolicy .

  • Delhi, India Qure.ai Full time

    About Qure.AI:Qure.AIis the world's fastest-growing medical AI company, boasting an impressive 18 FDA and 62 CE marking clearances to date. We develop cutting-edge solutions that significantly enhance patient outcomes across various care domains, including lung cancer, tuberculosis, and stroke. Our innovative technologies have positively impacted over 22...


  • Delhi, India RIGHT STAFF Full time

    Greetings from Right Staff One of our client who are into Medical Devices Are looking for a Regulatory Affairs person at Delhi NCR Job Description - **Experience minimum 5 Years and above compulsory** Designation - Regulatory Affairs/QA Affairs Time - Day Shift Location - Delhi NCR **Responsibilities**: - 1. Identify regulatory and post market...


  • Delhi, India ProPharma Full time

    We are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...


  • Delhi, India FLOAID MEDTECH Full time

    Location: IIT Madras Research park, Chennai, IndiaPosition Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time)Salary: Based on ExperienceCompany OverviewWe, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to provide...


  • Delhi, India FLOAID MEDTECH Full time

    Location: IIT Madras Research park, Chennai, IndiaPosition Type: Quality Assurance & Regulatory Affairs (QA/RA) Specialist(Full Time)Salary: Based on ExperienceCompany OverviewWe, “Floaid Medtech” is an evolving venture aiming towards the development of cutting edge medical devices, motivated with “Make In India” vision. Our own vision is to...


  • New Delhi, India OMC Medical Limited Full time

    Role Description This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...


  • New Delhi, India OMC Medical Limited Full time

    Role Description   This is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...


  • Delhi, Delhi, India Domnic Lewis International Full time

    We are seeking a highly skilled Regulatory Affairs Manager to join our team at Domnic Lewis International in BKC, Mumbai. This role is responsible for ensuring the highest professional standards in Regulatory Affairs and Pharmacovigilance to align with business objectives, values, and regulatory compliance.Key Responsibilities:Maintain and upload data to...


  • Delhi, India ProPharma Full time

    We are seeking ahighly skilled Regulatory Affairs AssociateorJunior Regulatory Affairs Managerwith proven expertise inVeeva Vaultto join our team on a6-month contractual basiswith the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined operations within...


  • delhi, India ProPharma Full time

    We are seeking a highly skilled Regulatory Affairs Associate or Junior Regulatory Affairs Manager with proven expertise in Veeva Vault to join our team on a 6-month contractual basis with the potential for extension. The ideal candidate will support regulatory data reconciliation and content management efforts, ensuring accurate and streamlined...


  • Delhi, Delhi, India Job Provider Baddi Full time

    Responsibilities: - Develop and implement regulatory strategies for drug development, registration, and commercialization in compliance with local and international regulations. - Coordinate regulatory submissions and responses to regulatory agencies, ensuring accuracy, completeness, and timeliness. - Maintain up-to-date knowledge of regulatory...


  • Delhi, Delhi, India Zuari Management Services Limited Full time

    About Zuari Management Services Limited: We are a leading provider of financial services, offering a wide range of products and solutions to meet the evolving needs of our customers. Our commitment to excellence drives us to deliver high-quality services.Job Title: Compliance OfficerThis role requires an individual with expertise in regulatory affairs,...


  • Delhi, Delhi, India OM Sai Management Consulting Services Full time

    Designation: - **Drug Regulatory Affairs-Male/Female** **JOB DESCRIPTION: -** - Delivery/Proper packing of goods for supplier - Maintaining the stock status at the back office - Settling of credit notes and following ups of payments from the parties - Coordinate with the vendors by keeping the track on purchase & delivery of orders sent - Maintaining the...


  • Delhi, Delhi, India Ample Leap Cognition & Technologies Pvt Ltd Full time

    DESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...


  • Delhi, Delhi, India OMC Medical Limited Full time

    Company OverviewOMC Medical Limited is a leading healthcare company based in the UK, specializing in regulatory services for medical devices. We offer comprehensive solutions to the healthcare industry.Job DescriptionThis is a full-time, remote-based role for a Regulatory Affairs Human Resources Specialist at OMC Medical Limited. The successful candidate...


  • Delhi, India Apsida Life Science Full time

    Regulatory Submission Manager (Immediate start)Collaborate with Global Regulatory Team Leads, and submission teams to ensure timely, high-quality regulatory submissions that comply with global guidelines and company SOPs. Provide mentorship and training to team members, fostering excellence and first-time-right...


  • Delhi, Delhi, India Professional Utilities Full time

    We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...


  • Delhi, India Domnic Lewis International Full time

    We are looking for an Assistant Manager- Regulatory Affairs and Pharmacovigilance for a Global Pharmaceutical MNC based in BKC, MumbaiPosition: Assistant Manager- Regulatory Affairs (Domestic market)Experience: 7+ in Regulatory affairs for domestic marketLocation: BKC, MumbaiPurpose of the Role:Ensure the highest professional standards in Regulatory Affairs...


  • new delhi, India OMC Medical Limited Full time

    Role DescriptionThis is a full-time on-site role for a Regulatory Affairs Associate at OMC Medical Limited. The Regulatory Affairs Associate will be responsible for handling regulatory documentation, ensuring regulatory compliance, understanding regulatory requirements, preparing regulatory submissions, and managing overall regulatory affairs for medical...


  • delhi, India Profile HR Consultants Pvt Ltd Full time

    CLIENT: Leading Pharma organization servicing regulated markets like US, Europe and developing markets of Africa and Asia.Key Drivers:Manage day-to-day regulatory operations along with quality assurance, implementation & Regulatory compliance in line with (GRP) Good Regulatory practice and cGMP best practices industry / Pharmaceutical field.Maintaining the...