1249 Mdr Jobs - Page 35

Job Description About The Role Exciting opportunity for an experienced Security Incident Responder to join our IT Security teamin Pune. Take a key role in driving success by enabling a seamless, global security incident response capability. This is a full-time, on-site position based in our Baner office. About You You have a curious mindset and are highly passionate about security engineering and the evolving role of AI in this domain. You also have: Experience between 2 to 5 years working as a SOC Analyst, Incident Responder or Detection Engineer. Knowledge applications of security frameworks DFIR, Cyber Kill Chain, MITRE ATT&CK. Confidence and the ability to remain calm under pressure. It ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Quality Engineer II for risk management & PSUR activities support for CST OU A Day in the Life Collaborating with cross-functional teams to develop comprehensive product risk management files, including the risk management plan, Hazard Analysis, DFMEA, and risk management report, adhering to ISO 14971 standards. Responsible for maintaining highest standards of product reliability and patient well-being through gather and analyze data, ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Responsibilities may include the following and other duties may be assigned Evaluates incoming complaint information and maintains the record in the electronic database. Performs follow up activities to obtain additional information. Use and maintain database(s), provide analysis and trending data all on complaints. Determines Reportability of complaints to Government Agencies. Identify and document appropriate complaint categories to ...

Hyderabad Job ID: SS202500077 Function: Quality Role: Regulatory Affairs Desired Skills: Regulatory, EU-MDR, Document, International Job Description Represent Regulatory Affairs as team member of product development projects from Concept through Commercialization. Review pre-clinical, and clinical protocols and associated reports to be used in submissions for assigned projects. Develop Regulatory Strategies for new or modified products for assigned projects. Bachelor’s degree in medical, Mechanical, Electric Life Science or other healthcare related majors Good relevant experiences for RA role in medical device and or pharmaceutical industry Good understanding for regulations and policies iss...

Job Description Job Overview: The Civil/Structural Designer provides solutions to problems in the Civil/Structural Design discipline without supervisory approval and will evaluate and select solutions from established operating procedures and/or scientific procedures. Responsibilities Key Tasks and Responsibilities: Prepare and develop arrangement and detail design drawings of high technical quality and professional consistent presentation, ensuring clarity and ease of construction Develop 3D models Ensure work complies with MDR and project QA and/or QC systems and procedures Apply basic technical skills and knowledge to complete assigned work Continue developing skills to efficiently comple...

Key Responsibilities: Supervise and manage daily production operations for nephrology-focused medical devices, ensuring alignment with the production schedule and quality requirements. Lead a team of production supervisors, operators, and technicians; assign responsibilities, monitor performance, and provide necessary training. Ensure all manufacturing processes comply with ISO 13485, GMP, FDA 21 CFR Part 820, EU MDR, and local regulatory guidelines. Collaborate with Quality Assurance, R&D, Maintenance, and Supply Chain teams to meet production goals and resolve issues. Monitor key performance indicators including productivity, yield, scrap rate, downtime, and on-time delivery. Drive continu...

Key Responsibilities: Develop and execute global regulatory strategies for nephrology medical devices. Prepare, compile, and submit regulatory filings including 510(k), CE Technical Files, MDR submissions, and country-specific dossiers. Maintain up-to-date knowledge of relevant global regulations including FDA, EU MDR, ISO 13485, MDSAP, and local regulatory frameworks. Serve as a regulatory representative in cross-functional product development teams. Ensure regulatory compliance throughout the product lifecycle, including labeling, advertising, change control, and post-market surveillance. Act as primary contact for regulatory agencies during audits, inspections, and query responses. Develo...

Description At AliveCor, we imagine a healthier world powered by access to personalized intelligent information. Heart disease kills more people than anything else in the western world, including all cancers combined. We're on a mission to be the worlds heart health partner by enabling access to quality heart care for everyone. AliveCor has pioneered over-the-counter medical EKG devices and continues to lead the way in empowering consumers and patients to take care of their heart. Using our FDA-cleared medical-grade hardware and software, hundreds of thousands of users have taken more than 100-million heart health measurements and counting. AliveCor seeks a Senior Regulatory Affairs Speciali...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Responsibilities may include the following and other duties may be assigned Evaluates incoming complaint information and maintains the record in the electronic database. Performs follow up activities to obtain additional information. Use and maintain database(s), provide analysis and trending data all on complaints. Determines Reportability of complaints to Government Agencies. Identify and document appropriate complaint categories to ...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Quality Engineer II for risk management & PSUR activities support for CST OU A Day in the Life Collaborating with cross-functional teams to develop comprehensive product risk management files, including the risk management plan, Hazard Analysis, DFMEA, and risk management report, adhering to ISO 14971 standards. Responsible for maintaining highest standards of product reliability and patient well-being through gather and analyze data, ...

Hello Connections, Looking for companies: Aujas Cybersecurity, Sattrix InfoSec, Infopercept, Eventus Security, Network Intelligence (NII), Ziroh Labs, Riskpro India Job Title: Cybersecurity Sales Manager USA Market (SOC Services) Location : India (Remote / Pune / Mumbai / Bengaluru / NCR) Experience : 5+ years in International IT / Cybersecurity Sales (USA Market) About the Role We are seeking a high-performing Sales Manager to drive business growth for our Managed SOC (Security Operations Center) services in the United States . The ideal candidate will have a strong background in cybersecurity, cloud security, SIEM/SOAR , and selling to mid-market or enterprise clients in the U.S. region. K...

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meani...

About the position Position Title Sr Manager - Finance Location Gurgaon Business Unit Finance Function Finance & Accounts Reporting Manager Finance Controller Team Size 5 You can become a part of … … a truly aspirational brand, one of India’s fastest growing fintech companies that offers a range of financial services & products for merchants, kirana store owners and end consumers. Valued at over $2.8 Bn within a short span of 3+ years, we focus on empowering small business owners and retailers with business ranging from QR & PoS payments to easy loans to high-yield investment products which in turn enables them to grow and transform. We understand that business and culture are two sides of t...

About Us Sophos is a global leader and innovator of advanced security solutions for defeating cyberattacks. The company acquired Secureworks in February 2025, bringing together two pioneers that have redefined the cybersecurity industry with their innovative, native AI-optimized services, technologies and products. Sophos is now the largest pure-play Managed Detection and Response (MDR) provider, supporting more than 28,000 organizations. In addition to MDR and other services, Sophos’ complete portfolio includes industry-leading endpoint, network, email, and cloud security that interoperate and adapt to defend through the Sophos Central platform. Secureworks provides the innovative, market-l...

Company Description iSecurify, a specialized division of Allianz I, is a next-generation cybersecurity and GRC (Governance, Risk & Compliance) startup on a mission to simplify and democratize security, making it accessible and effective for businesses of all sizes. Created from the strategic vision of Allianz I, iSecurify addresses the growing threats in the digital landscape. We aim to be known for innovation, reliability, and customer-centric solutions in the cybersecurity space. We provide a comprehensive suite of services, including SIEM as a Service, MDR, vCISO, VAPT, phishing simulations, Cybersecurity and Compliance trainings, web app code analysis, and regulatory compliance solutions...

Security represents the most critical priorities for our customers in a world awash in digital threats, regulatory scrutiny, and estate complexity. Microsoft Security aspires to make the world a safer place for all. We want to reshape security and empower every user, customer, and developer with a security cloud that protects them with end to end, simplified solutions. The Microsoft Security organization accelerates Microsoft’s mission and bold ambitions to ensure that our company and industry is securing digital technology platforms, devices, and clouds in our customers’ heterogeneous environments, as well as ensuring the security of our own internal estate. Our culture is centered on embra...

We’re AtkinsRéalis, a world class Engineering Services and Nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. Created by the integration of long-standing organizations dating back to 1911, we are a world-leading professional services company dedicated to engineering a better future for our planet and its people. We deploy global capabilities locally to our clients and deliver unique end-to-end services across the whole life cycle of an asset including consulting, advisory...

Dear Candidate, Currently we require Regulatory Manager for Medical device. Location - Sohna, Haryana Cab facility Available for Gurugram or Faridabad candidates. Minimum Experience - 4+ years in Medical devices Job profile: Key responsibilities: Spearheaded regulatory submission strategy for CE marking under EU MDR for Class IIa, IIb & III devices. Authored and maintained FDA 510 (K) submission, including predicate device comparison and labeling review. Developed and maintained Technical Files and Design Dossier for European markets. Coordinated Clinical Evaluation Reports (CER) and Periodic Safety Update Reports (PSUR). Acted as point-of-contact for notified bodies and regulatory authoriti...

Capture LEADS – demonstrate steps to Link, Like & Love York Newspapers and other local associated publications on Facebook, news.com sites, reporter email / newsletters, and more Build specific, market development (prospecting) plans for the MDR team Coach salespeople to develop their sales skills including vertical market knowledge, forecasting, prospecting, and other necessary skills, while maintaining individual accountability to goals Develop and execute sales process and strategies and ensure compliance to internal data management and reporting, including use of Salesforce.com Recommend and implement improvements to achieve sales and opportunity creation goals Proactively communicate re...

LTTS India Vadodara Job Description  Ensure Project documents are timely controlled, accessible and current at all project locations.  Maintain accuracy of the Project Document Distribution Matrix (DDM) based upon input by Project Team.  Facilitate and coordinate the flow of all Project deliverables, internally generated and Contractor provided.  Report progress in completion of deliverables, issue look ahead, and overdue reports.  Comprehend and enforce the Document Management sections of Project Plans, Contract Coordination Procedures, and Purchase Orders. o Confirm accuracy of Master Document Registers (MDRs). Validate against Project Electronic Document Management System. Report inc...

About Us Sophos is a global leader and innovator of advanced security solutions for defeating cyberattacks. The company acquired Secureworks in February 2025, bringing together two pioneers that have redefined the cybersecurity industry with their innovative, native AI-optimized services, technologies and products. Sophos is now the largest pure-play Managed Detection and Response (MDR) provider, supporting more than 28,000 organizations. In addition to MDR and other services, Sophos’ complete portfolio includes industry-leading endpoint, network, email, and cloud security that interoperate and adapt to defend through the Sophos Central platform. Secureworks provides the innovative, market-l...

Dear Candidate, Currently we require Regulatory Manager for Medical device. Location - Sohna, Haryana Cab facility Available for Gurugram or Faridabad candidates. Minimum Experience - 4+ years in Medical devices Job profile: Key responsibilities: Spearheaded regulatory submission strategy for CE marking under EU MDR for Class IIa, IIb & III devices. Authored and maintained FDA 510 (K) submission, including predicate device comparison and labeling review. Developed and maintained Technical Files and Design Dossier for European markets. Coordinated Clinical Evaluation Reports (CER) and Periodic Safety Update Reports (PSUR). Acted as point-of-contact for notified bodies and regulatory authoriti...

Job Title Norm Compliance Officer Job Description Norm Compliance Officer The purpose of this position is to handle end-to-end Norm Compliance activities for Diagnostic X-ray systems as part of the Research and Development team, with all relevant mandatory international and national regulations. Your role: Defining all applicable global product safety certification, product safety, EMC and environmental (if applicable) standards like IEC, EN, and ISO standards required to comply with all applicable international regulations. Define and review product requirements related to guidance, codes and standards to assure norm compliance and decomposition of standard requirements to the individual sy...

Job Title: Software MedTech Technical/Functional Skills: Must have skills Desired Competencies (Technical/Behavioral Competency) Hands-On experience of acting as a primary subject matter expert in the field of Medical Device FW Architecture, Modeling, Design and Development Lead delivery of safety critical embedded Systems and application software for Medical Devices. Experience in architecture, modeling, requirements definition, development, developing requirements and specifications, project planning, execution, management, and documentation to ensure compliance to SDLC, policies and procedures. Excellent Knowledge of Medical Device Design Control Requirements for regulatory compliance Exp...

MISSION STATEMENT To ensure the quality lifecycle management for dedicated, subcontracted, product portfolio. Qualified auditor. Main Accountabilities And Duties Operational skills Operational quality management of a dedicated product portfolio which includes: Quality management of deviation and complaint records and their related CAPAs Assessment and management of change controls Edition of QA Agreements with Zentiva third parties and subcontractors Collection and evaluation of PQRs and stability data Compliance evaluation of Third Parties and products Maintenance of product database Collection and review of CoA/CoC QA support of product launches and transfers GMP, GDP, MDR, HACCP, Food Sup...