1256 Mdr Jobs - Page 48

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: Manager - Enterprise Business Company: Techdefence Labs Solutions Ltd. Location: Pune, Bangalore, Hyderabad, Kolkata Experience: 3+ years Type: Full-Time | Individual Contributor About Techdefence: Techdefence Labs Solutions Limited is a leading cybersecurity company, providing cutting-edge security services, compliance solutions, managed security offerings, and the sale of best-in-class cybersecurity OEM products. We protect enterprises by combining technical depth, threat intelligence, and industry experience to create robust security postures across industries. Role Overview: We are seeking a technically proficient and strategically minded Manager – Enterprise Business to drive...

Job Title: Wire Cutting Operator – Ortho & Pharma Components Location: Chrompet, Chennai Experience: 2 to 3 Years Qualification: ITI / Diploma / BE (Mechanical or relevant discipline) Gender: Male Salary: ₹23,000 Net Take Home Interview Mode: Face-to-Face Job Responsibilities:Study engineering drawings and generate wire cutting programs accordingly. Operate wire cutting machines efficiently and accurately. Adhere strictly to safety norms and practices in the workplace. Ensure proper identification and traceability of components during production. Maintain compliance with ISO 13485, EU MDR 2017/745, and MDD standards. Keep accurate and up-to-date QMS records related to production and machine ...

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...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and de...

1. University degree level or equivalent through experience and professional certification. 2. A minimum of 7-10 years in Security and Loss prevention role, law enforcement or security-related profession. 3. Extensive and up to date knowledge of Shrink management and Data Analysis. 4. Experience in managing or coordinating security investigations of complex nature. 5. Knowledge of information security processes and systems. 6. Experience in security auditing Job Description: The primary objective of the SLP Specialist is to provide security services, investigation and asset protection in designated area of responsibility, assist in mitigating product loss, and maintain customer satisfaction ...

Title Principal Technical Professional-Instrumentation/Controls Shall be responsible for Planning of all Deliverables related to the identified Commodity. Shall review the Level-3 schedule, MDR dates, shall co-ordinate with all relevant disciplines for required interface. Shall be responsible for identifying the inputs that are required all the Engineering deliverables pertaining to that commodity. Shall check the P&IDs and instrument index and shall ensure that all tags are covered as per issued P&IDs. Shall be responsible for maintaining the tracker for all Engineering deliverables pertaining to that commodity. Shall be responsible for ensuring good quality deliverables. Shall provide tech...

About Us We help progressive enterprises navigate the new reality of digital risks with proactive and intelligent cybersecurity. Job Description At Scybers, we’re seeking a sharp, vigilant, and dynamic Detection & Response Lead to join our Managed Detection and Response (MDR) team. Step into a pivotal role where every day brings new challenges, and your strategic decisions will have a significant impact on our clients’ security. What You Will Do, Handle client engagements and work as the point of contact for MDR projects Drive the implementation of emerging threat intelligence (IOCs, updated rules, etc.) to identify affected systems and the scope of the attack. Implement standards and proced...

Position :- Mechanical Design Engineer - EU MDR Support Experience : - 5-7 Years Work location:- Gurgaon Qualification :- BE/B.Tech/ Master’s degree in Mechanical/ Design Engineering Notice Period :- Immediate to 30 Days Domain :- Medical (Mandatory) Key Responsibilities: - Experience of 5-7 years in Medical device industry. Exposure to good Documentation Practices and understanding of Design input/ Output/ Verification deliverables. Exposure to EUMDR or regulatory requirements will be added advantage. Exposure to new technologies and current industry practices are expected Quick learner and should be able to deliver with minimum intervention. Good verbal and Written Communication Skills. Qu...

2+ years of experience in medical device regulatory affairs EU MDR, US FDA 510(k) and closely working R&D, Quality organizations. Experience creating Technical Documentation and 510(k) preparation and receiving submission approval (EU, US, Canada etc.) Expertise in interpreting and implementing various medical device standards and guidance's, such as IEC 60601-1, ISO 14971-1, IEC 62366-1, ISO10993-1, and MEDDEV 2.7/4. Experience with systems for quality management, product development, and follow-up of procedures is an advantage. Knowledge and application of medical device QMS is required (e.g., ISO 13485, MDSAP, EU MDR, Risk Management etc.) Personality Characteristics Be able to handle ad-...

Qualifications: Bachelor's or Master's degree in Engineering, Biomedical, Life Sciences, or a related field. Minimum of 12 years of experience in risk management within the medical device industry . In-depth knowledge of ISO 14971 and global regulatory requirements (FDA, EU MDR/IVDR, TGA, etc.). Strong background in risk analysis tools: FMEA, FTA, HACCP, etc. Experience with Class II/III medical devices preferred. Excellent problem-solving, analytical, and decision-making skills. Strong communication and leadership skills. Experience working in cross-functional, global teams. Certifications such as RAC, CQE, or Six Sigma are a plus. Show more Show less

Company Description Genuine Biosystem Pvt Ltd (GBPL) has emerged as a prominent company in the Indian market over the last 13 years. We specialize in the production of Invitro Diagnostic (IVD) reagents and kits, and Laboratory Medical equipment, all adhering to the highest production standards. Our research team is equipped to respond quickly to market demands and ensure customer satisfaction by offering personalized service and cost-effective solutions. Our products are ISO & CE certified, and our production site is recognized by MDR 2017. Role Description This is a full-time, on-site role as an IVD QC Manager located in Chennai. The IVD QC Manager will be responsible for overseeing the qua...

Our Mission At Palo Alto Networks® everything starts and ends with our mission: Being the cybersecurity partner of choice, protecting our digital way of life. Our vision is a world where each day is safer and more secure than the one before. We are a company built on the foundation of challenging and disrupting the way things are done, and we’re looking for innovators who are as committed to shaping the future of cybersecurity as we are. Who We Are We take our mission of protecting the digital way of life seriously. We are relentless in protecting our customers and we believe that the unique ideas of every member of our team contributes to our collective success. Our values were crowdsourced...

Job Description Key Accountabilities Managing project related documents with accuracy and quality in timely manner. Control all aspects of projects documentation on multiple projects a assigned keeping alignment with Client systems and procedures. Upon Project award, prepare Work List for Project as advised by PM / Project Planner and release to trades. Create project specific email address and ensure department distributions are made, as per project requirement and distribution strategy is in place. Arrange to grant project/network drive access and give authorization as per Company policy. Ensure to develop project folder structure upon award and all project documents are kept in relevant p...

Job Title: Head – Quality Assurance & Regulatory Affairs (Medical Devices) Location: Visakhapatnam /Chennai Position Type: Full-Time Experience Level: Senior (Individual Contributor + Leadership Oversight) Reports To: CEO / COO / Head of Operations About the Role We are looking for a highly experienced and execution-driven QA/RA professional to lead our Quality and Regulatory function as we scale medical device manufacturing under FDA and EU MDR frameworks. This role is ideal for someone who combines deep regulatory expertise with a hands-on approach —someone who leads by doing, not just directing. You will be responsible for establishing and maintaining the entire Quality Management System ...

At Capgemini Invent, we believe difference drives change. As inventive transformation consultants, we blend our strategic, creative and scientific capabilities,collaborating closely with clients to deliver cutting-edge solutions. Join us to drive transformation tailored to our client's challenges of today and tomorrow.Informed and validated by science and data. Superpowered by creativity and design. All underpinned by technology created with purpose. The GxP CSV Validation Engineer ensures that digital systems used in clinical development comply with regulatory standards (GxP, 21 CFR Part 11, EMA Annex 11). They develop and execute validation protocols (IQ, OQ, PQ), risk assessments, and doc...

We currently looking for Medical Device Affairs and Compliance Specialist for one of our entity Faith Innovations. please find the following Job Description. 1. Designation:- Compliance Specialist ( Male only ) Salary:- 25K -35K/PM Location:- Delhi Company:- Faith Innovations No. of positions 01 Educational Qualification: B. Tech (Electrical & Mechanical engineering) Experience: Mandatory: 2-3 yr in the medical devices QA/RA Drive completion of compliance requirements whenever assigned by the Compliance team and/ or Function head i.e., to update and review records and documents for completeness and compliance as per MDR and ISO requirements Ability to understand the classification of medical...

It’s not just about your career or job title… It’s about who you are and the impact you will make on the world. Because whether it’s for each other or our customers, we put People First. When our people come together, we Expand the Possible and continuously look for ways to improve what we create and how we do it. If you are constantly striving to grow, you’re in good company. We are revolutionizing the way the world moves for future generations, and we want someone who is ready to move with us. Role: To perform end to end operations related activities, transactions, documentations and records Key Responsibilities: Responsible for Engineering operations related activities Position: – Enginee...

Job description DESIGNERS AUTOCAD Job description Responsibilities Prepare project documentation, deliverables list, MDR and track the project on regular basis and report to the senior project team. Carry out structural engineering calculations using first principles and FEA methods. Work independently or as part of the project team, ensure that the projects are delivered in accordance with the client contract requirements. Conduct project meetings and attend occasional onsite inspections. Collaborate with other disciplines and members of the DIMENSION regarding operational and specialist matters. Work together with relevant consultants, authorities, customers, and clients to ensure that all...

Job Title: Technical Writer Intern – Regulatory & Engineering Documentation Location: Chennai, India (Onsite – IIT Madras Research Park) Employment Type: Internship (6 months, fixed) Stipend: ₹10,000 – ₹20,000/month Requirement: Bachelor's/Masters in Mechanical, electronics, biomedical engineering 🧬 About Floaid Floaid is a MedTech startup pioneering next-generation cardiac assist technologies. We work at the intersection of innovation, precision engineering, and regulatory compliance to create life-saving medical devices. 🔍 Role Overview We are seeking a detail-oriented Technical Writer Intern to support our multi-disciplinary engineering and regulatory teams. You will be responsible for pr...

Description INSLP (Security & Loss Prevention) is hiring an SLP Specialist to support growth of the “SLP MDR Concessions Abuse Program” and help preventing losses via identification of abusive entity. The program is aimed at identifying and eliminating Concessions Abuse while preserving customer trust. The primary objective of the SLP Specialist is to provide security services, investigation and asset protection in designated area of responsibility, assist in mitigating product loss, and maintain customer satisfaction in accordance with INSLP guidelines and policies. The role is cross-functional and requires deep collaboration and influencing ability with stakeholders from business and corpo...

Principal Engineer, Security Operations The Principal Engineer, Security Operations at Vimeo will play a pivotal role in leading and implementing security strategies and initiatives designed to protect our vast user base of over 300 million users and their valuable content. This role requires close collaboration with multiple teams across the organization, including Development, DevOps, Infrastructure Security, Compliance, IT, and Product, to ensure a holistic and effective security posture. You will be at the forefront of safeguarding sensitive user data and critical systems from a constantly evolving threat landscape. This includes proactively identifying and addressing vulnerabilities, im...

Ankura is a team of excellence founded on innovation and growth. Location: Conditional Remote / Gurgaon Hours: 40 hours a week Reporting: Director - Threat Detection Operations (TDO) Duties include continuous monitoring of Security Information Event Management (SIEM), EDR, XDR, DLP and related platforms for correlated events and alerts and working with the client to take action. Analysts leverage events to determine the impact, document possible causes, and provide useful information to clients. A deep understanding of various commercial and open-source network sensors, intrusion detection systems, and event log correlation engines is required as analysts are expected to deliver enhanced thr...

Responsibilities Regulatory Strategy & Compliance – US FDA, EU MDR, CDSCO Documentation & Regulatory Submissions Regulatory Monitoring & Reporting UDI Submission – GUDID / EUDAMED Regulatory Audits, Inspections, CAPAs & NCs Closure Qualifications BE/BTech in Mechanical, Biomedical, Biotech, or related fields Min 2 years of exp. in RA for medical devices Knowledge of U.S. FDA, EU MDR, CDSCO regulations RAC/GATE certification is a plus Show more Show less

About The Position Snowbit is a cybersecurity technology innovator with a vision to empower organizations across the globe to quickly, efficiently, and cost-effectively ready themselves to address omnipresent cyber risk. Built off years of Israeli cybersecurity experience, Snowbit is looking to offer the broadest managed detection and response offering available today. Snowbit is part of the Coralogix group, with Coralogix rebuilding the path to observability by offloading the burden of indexing and providing deep insights, at an infinite scale, for less than half the cost. We are looking for experienced and highly motivated Senior Cloud Security Analysts to join our journey and be a part of...