Director Quality Regulatory Affairs
5 days ago
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 .
-
Director Quality Regulatory Affairs
4 days ago
Delhi, India Qure.ai Full timeAbout 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 Qure.ai Full timeAbout 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...
-
Vacancy for Regulatory Affairs at Delhi Ncr
5 months ago
Delhi, India RIGHT STAFF Full timeGreetings 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...
-
Regulatory Affairs Specialist
1 week ago
delhi, India Apsida Life Science Full timeApsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.Immediate start!!!You will need toProvide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore...
-
Regulatory Affairs Specialist
1 week ago
delhi, India Apsida Life Science Full timeApsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.Immediate start!!!You will need toProvide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore...
-
Regulatory Affairs Specialist
1 week ago
Delhi, India Apsida Life Science Full timeApsida Life Science are looking for a Regulatory Affairs Specialist for a long term project.Immediate start!!!You will need toProvide regulatory advice, verify strategic approaches and timelines, and align zone strategies with Affiliate Regulatory Affairs teams.Apply knowledge of regulatory requirements in Vietnam, Philippines, Thailand, Malaysia, Singapore...
-
Regulatory Affairs Expert
4 weeks ago
Delhi, Delhi, India SVKM's Narsee Monjee Institute of Management Studies (NMIMS) Full timeJob Title: Professor / Associate Professor / Assistant ProfessorJob Description:We seek a highly qualified and experienced academic to join our esteemed faculty at Shobhaben P.Patel School of Pharmacy & Technology Management, Mumbai Campus. The successful candidate will be responsible for teaching and research in the area of Regulatory...
-
Regulatory Affairs Manager
13 hours ago
Delhi, India Medisal Pharma - Medisal for Pharmaceuticals Industry LLC Full timeAbout Medisal PharmaAs a proud United Arab Emirates company based in Abu Dhabi, Medisal Pharma is dedicated to excellence in manufacturing high-quality pharmaceutical products to enhance global health by developing and delivering high-quality, affordable medicines. With a strong emphasis on innovation, research, and excellence, we aim to make a significant...
-
Regulatory Affairs Manager
1 day ago
Delhi, India Medisal Pharma - Medisal for Pharmaceuticals Industry LLC Full timeAbout Medisal PharmaAs a proud United Arab Emirates company based in Abu Dhabi, Medisal Pharma is dedicated to excellence in manufacturing high-quality pharmaceutical products to enhance global health by developing and delivering high-quality, affordable medicines. With a strong emphasis on innovation, research, and excellence, we aim to make a significant...
-
Regulatory Affairs Expert
3 weeks ago
Delhi, Delhi, India ELT Corporate Private Limited Full timeJob Title: Regulatory Affairs ExpertJob Summary: We are seeking an experienced Regulatory Affairs Expert to support our market research efforts by identifying potential clients needing BIS certifications, staying updated on relevant regulations, and collaborating across teams to align research insights with our business objectives.Key Responsibilities:Track...
-
Regulatory Affairs Executive
2 months ago
Delhi, India Ipca Laboratories Limited Full timePosition : Executive - Regulatory affairs formulation for USA market.Qualification : B.Pharm/M.Pharm Experience : 4 - 7 years experience of working in regulated markets like USA/ Europe/Australia with experience of ANDA, USA market preferred.Role:Preparation of registration dossiers as per the US Regulatory guidelines Preparation of renewal application as...
-
Regulatory Affairs Officer
6 months ago
Delhi, India NKG ADVISORY BUSINESS AND CONSULTING SERVICES PVT LTD Full timeRegulatory Affairs Specialist - Legal Metrology and EPR India **Responsibilities**: Regulatory Compliance: Stay up-to-date with the latest Legal Metrology and EPR regulations in India. Ensure that all products and processes comply with these regulations. Documentation: Prepare and maintain all necessary documentation required for regulatory submissions,...
-
Regulatory Affairs Specialist
3 weeks ago
Delhi, Delhi, India Danaher Full timeRegulatory Affairs SpecialistThe Regulatory Affairs Specialist will play a key role in ensuring compliance with regulatory requirements for medical devices in India, Sri Lanka, and other SWA countries. This includes preparing and submitting regulatory submissions, interacting with regulatory agencies and health authorities, and ensuring timely product...
-
Regulatory Affairs Specialist
3 weeks ago
Delhi, Delhi, India Danaher Full timeAt Danaher, we're seeking an experienced Regulatory Affairs Specialist to join our team and contribute to the success of our organization.The ideal candidate will have a strong background in regulatory affairs, with a focus on the medical device industry. They will be responsible for coordinating with cross-functional departments to ensure compliance with...
-
Drug Regulatory Affairs
5 months ago
Delhi, Delhi, India Job Provider Baddi Full timeResponsibilities: - 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...
-
Regulatory Affairs Strategist
3 weeks ago
Delhi, Delhi, India ResMed Full timeThe Regulatory Affairs function at ResMed plays a vital role in ensuring the company's products comply with regulatory frameworks. Key responsibilities include providing support and guidance throughout the product life cycle, ensuring compliance, and delivering optimal regulatory strategies.Database Management: Support and maintain internal and government...
-
Regulatory Affairs Specialist
3 weeks ago
Delhi, Delhi, India ELT Corporate Private Limited Full timeJob Title: Regulatory Affairs SpecialistAbout Us: ELT Corporate Private Limited is a leading regulatory consultancy specializing in Compliance, Registrations, Licensing, and Legal Services. Our areas of expertise include handling regulatory requirements for import-export, Medical Device Registration, Legal Metrology, Environmental Regulatory Compliance, BIS...
-
Senior Drug Regulatory Affairs Manager
4 weeks ago
Delhi, Delhi, India OS Mgmt Consulting Services Full timeJob Title: Senior Drug Regulatory Affairs ManagerJob Summary: We are seeking a highly skilled Senior Drug Regulatory Affairs Manager to join our team at OS Mgmt Consulting Services. As a Senior Drug Regulatory Affairs Manager, you will be responsible for ensuring compliance with drug regulatory requirements and managing our relationships with vendors and...
-
Drug Regulatory Affairs
5 months ago
Delhi, Delhi, India OM Sai Management Consulting Services Full timeDesignation: - **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...
-
Regulatory Affairs Executive
6 months ago
Delhi, Delhi, India Ample Leap Cognition & Technologies Pvt Ltd Full timeDESIGNATION/ 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...