906 Mdr Jobs - Page 16

Job Summary: We are seeking a highly motivated and detail-oriented Assistant/Deputy Manager – Regulatory Affairs & Liaisoning with specialized experience in In-Vitro Diagnostics (IVD), specifically including Rapid Card Tests, CLIA, ELISA, Clinical Chemistry, Hematology and RT-PCR. The ideal candidate will have strong hands-on experience in regulatory filing (DMF, technical documentation, application preparation and follow-up), product licensing, and regulatory liaisoning with national and international regulatory bodies. Key Responsibilities: Regulatory Submissions & Filings: Prepare and submit Device Master Files (DMF)/Product Dossiers, and Technical Documentation in accordance with CDSCO o...

Position: Cybersecurity Enterprise Sales – SIEM Engineering Focus Experience : 8+ Location: Hyderabad/Bangalore/Mumbai Role Overview: We are seeking a dynamic and results-driven Cybersecurity Enterprise Sales professional to join our team. This role is focused on selling advanced cybersecurity solutions, including SIEM, SOAR, and Adaptive MDR offerings, to mid-to-large enterprises. The ideal candidate will have a strong foundation in cybersecurity operations, particularly SIEM engineering, and a proven track record in enterprise technology sales Key Responsibilities: • Develop and execute a strategic sales plan to meet and exceed quarterly and annual sales targets. • Identify, qualify, and p...

DESCRIPTION Amazon’s SLP team is seeking highly skilled and motivated person to help develop a and implement a world class security program for our first mile network which will ensure that our customers receive the items they purchase on time and at the best possible cost. Amazon is one of the most recognizable brand names in the world and we distribute millions of products each year to our loyal customers. The SLP Specialist – MDR Return, will be responsible for partnering with respective stakeholders and prog teams spread across various cities within a region to execute company security policies and provide security services and asset (lives, inventory in transit and within sort center, b...

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...

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...

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...

Job Title Senior Regulatory Affairs specialist Job Description Job title: Senior Regulatory Affairs Specialist Your role: Developing and executing the regulatory strategy for new product development, design changes and field safety corrections for US, EU, Canada and RoW. Participate in strategic product development, design solutions from the concept phase to the product delivery phase and provide regulatory guidance throughout design and development. Responsible for product registrations/approvals for their responsible products within IGT-S portfolio. Author and lead 510(k) submissions, pre-sub meetings, EU MDR Technical Documentation, and Health Canada license applications. Lead interaction...

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...

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...

📢 Hiring Alert | Job Opening in Medical Devices Industry Position: Application for Medical Device Vigilance Specialist (Preferred Immediate Joiner) Location: Hyderabad Language Requirement: Fluent in Polish is must Key Responsibilities: Bachelor’s or master’s degree in pharmacy, Life Sciences, Biomedical Engineering, or related field. 2-4 years of experience in experience in complaint handling medical devices , Investigations, and/or Vigilance within a regulated industry (pharma or medical devices). Strong understanding of global regulatory requirements and standards (e.g., FDA QSR, ISO 13485, EU MDR, GVP). Experience with complaint management and safety databases (e.g., Track Wise, Aris, Sa...

About Halma: Halma is a global group of life-saving technology companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US. Our diverse group of nearly 50 global companies specialise in market leading technologies that push the boundaries of science and technology. For the last 42 years, the combination of our purpose, strategy, people, DNA and sustainable business model has resulted in record long-term growth in revenues and profits and an increase in dividend by ≥ 5% every year– an achievement unrivalled by any company listed on the London Stock Exchange. Why join us...

Function:PMSRole:Post Market SurveillanceDesired Skills:PMS, complaint handlingCreate PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis Risk management Risk assessment. Required Candidate profile Propose strategies and solutions to data issues or challenges that occur during the PSUR writing and conclusion process.

Sales Director – Cybersecurity Tools (Enterprise & BFSI Sector) Experience: 12–20 years Industry: Cybersecurity, BFSI, Enterprise IT Employment Type: Full-time, Leadership Role Role Overview We are seeking a dynamic and strategic Sales Director to spearhead our cybersecurity solutions sales within the Enterprise and BFSI sectors across India. This leadership role demands a seasoned professional with a proven track record in enterprise sales, particularly in cybersecurity, and the ability to engage with C-level stakeholders to drive business growth. Key Responsibilities Strategic Sales Leadership: Develop and execute a robust sales strategy targeting enterprise and BFSI clients, aligning with...

SaMD/SIMD Regulatory Affairs Executive Key Responsibilities: Prepare, compile, and submit regulatory documentation for SaMD/SIMD products, including 510(k), CE marking (under MDR), UKCA, and other global regulatory submissions. Ensure SaMD product development and maintenance align with relevant standards such as IEC 62304 , ISO 14971 , ISO 13485 , ISO 27001 , and applicable cybersecurity guidance. Maintain up-to-date knowledge of regulatory requirements and guidance related to SaMD (e.g., FDA’s premarket guidance, EU MDR Annex VIII, IMDRF SaMD framework). Provide regulatory input into product design and development documentation, including risk management, clinical evaluation, and labeling. ...

Job Title: Regulatory Affairs Specialist Location: Devine Meditech, Okhla phase -1, New Delhi Experience Required: 3–5 Years Industry: Medical Devices / Healthcare / Surgical Equipment Salary Range: ₹30,000 – ₹50,000 per month (negotiable based on skills and experience) Reporting to: Head – Quality & Regulatory Affairs Job Summary: Devine Meditech is seeking a dynamic and detail-oriented Regulatory Affairs Specialist with 3–5 years of experience in the medical devices industry. The role involves ensuring product compliance with Indian and international regulatory requirements, preparing regulatory submissions, and maintaining up-to-date product documentation in line with applicable standards...

Technical Support Engineer (L1) – Cybersecurity Location: Viman Nagar, Pune (Hybrid: 3 days WFO, 2 days WFH) Experience: 5+ Years Rotational Shift Contact us- 7876212244 We need experts in server-side troubleshooting . Required Skills & Experience: Good understanding of Windows networking concepts. Knowledge of networking (preferably with exposure to CCNA-level concepts ). Ability to differentiate between network-related and system-related issues . Hands-on experience or strong knowledge of Virtual Machines (VMs) , including maintenance and troubleshooting. Experience in providing technical support to American or global customers in an IT support environment. Exposure to Windows or Linux sys...

Medical Mechanical Design Verification/Control Engineer- WalkIN on 21st July in Chennai Shollinganallur Join a team that values innovation, growth, and impactful work. Don’t miss the chance to work with cutting-edge Project in SME and be a part of something transformative! 📅 Drive Date:21st July Saturday (9AM-2PM) Contact Person: Katherine Sylvia/Swarali 📍Venue Location: #HCLTech Elcot Sez, 602/3, 138, Medavakkam High Road, Sholinganallur, #Chennai -600119 Position:Mechanicaldesign (Lead, Technical Lead /Sr Lead) 👤Experience: 3-7 years 📍Job Location:Chennai Skill : Medical device, Design control, Design Verification, DHF, MDR, ISO13485, Risk management, Design #JD : B.E / B.Tech or higher ed...

Job Description for the Role of Team Lead - Compliance Job Title: Team Leader – Compliance Department: Compliance Location: Ambernath, Experience Required: 7+ Years Job Summary: The Lead – Regulatory Compliance is responsible for ensuring that the organization’s electronic medical and industrial devices comply with applicable domestic and international regulatory requirements. This role demands strategic oversight of regulatory submissions, audits, training, and quality system management, including US FDA , ISO 9001:2015 , ISO 13485:2016 , MDR 2017/745, MDR (India) and MDSAP . The position acts as a key liaison between regulatory authorities and internal departments, promoting a culture of c...

As a Sales Specialist for Cybersecurity & GRC Solutions at iSecurify, a pioneering division of Allianz I dedicated to simplifying and democratizing security, you will play a crucial role in driving the growth and success of our next-generation cybersecurity and GRC products. Based in Vadodara, you will be part of a dynamic and innovative team that is reshaping the security and GRC landscape with cutting-edge solutions like SIEM, MDR, vCISO, VAPT, SOC, and our powerful Single Pane of Glass (SPOG) platform. Your responsibilities will involve developing and executing sales strategies in collaboration with leadership, conducting market research to identify opportunities and ideal client profiles...

Looking to kickstart your career in Technology or Cybersecurity Sales? We’re offering a 4-month unpaid Sales & Marketing Internship exclusively for BBM or MBA graduates (2023–2024 passouts only). This is ideal for freshers who want to: ✅ Break into B2B Technology & Cybersecurity Sales ✅ Learn Pre-sales, Inside Sales & Growth Marketing ✅ Work closely with industry veterans and gain real-time, hands-on experience in one of the fastest-growing sectors 🔹 Internship Type : Unpaid (4 Months) 🔹 Location : Remote / Hybrid 🔹 Opportunity for a full-time role based on performance 💰 Performance Incentives for successful lead closures as a gesture of goodwill and encouragement 🚀 Why Cybercommand? We’re a...

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and i...

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and i...

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and i...

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and i...

Come join Deepwatch’s team of world-class cybersecurity professionals and the brightest minds in the industry. If you're ready to challenge yourself with work that matters, then this is the place for you. We're redefining cybersecurity as one of the fastest growing companies in the U.S. – and we have a blast doing it! Who We Are Deepwatch is the leader in managed security services, protecting organizations from ever-increasing cyber threats 24/7/365. Powered by Deepwatch’s cloud-based security operations platform, Deepwatch provides the industry’s fastest, most comprehensive detection and automated response to cyber threats together with tailored guidance from dedicated experts to mitigate r...