907 Mdr Jobs - Page 20

Position: Quality Engineer, Post Market Surveillance (Contractor Role) Job Title: Quality Engineer Quality Engineer, PMS - Individual Contributor Reports to: Associate Manager, PMQ Trauma & Extremities Budget: 7-8 LPA Location: Gurugram Notice: Immediate -30 Days Experience: 2-4 Years Roles and Responsibilities The Quality Engineer will work on all the various aspects of Post Market Surveillance and enters customer complaints into the company-wide complaint handling system and follows methods to analyze the complaints, for the Trauma & Extremities business. He/She should be competent to compile the Product Safety Usage Reports (PSURs) independently. These activities as they relate to Post Ma...

Position: Quality Engineer, Post Market Surveillance (Contractor Role) Job Title: Quality Engineer Quality Engineer, PMS - Individual Contributor Reports to: Associate Manager, PMQ Trauma & Extremities Budget: 7-8 LPA Location: Gurugram Notice: Immediate -30 Days Experience: 2-4 Years Roles and Responsibilities The Quality Engineer will work on all the various aspects of Post Market Surveillance and enters customer complaints into the company-wide complaint handling system and follows methods to analyze the complaints, for the Trauma & Extremities business. He/She should be competent to compile the Product Safety Usage Reports (PSURs) independently. These activities as they relate to Post Ma...

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 Prepare and compile product post market data and findings into comprehensive Periodic Safety Update Reports (PSURs) in compliance with regulatory requirements. Serving as a mentor to junior engineers, providing guidance and support in quality engineering practices within the realm of medical devices. Responsibilities may include the following and other duties may be assigned Familiar with ISO 9001, ISO 13485, ISO 14971, 21 CFR part 820...

India - Hyderabad JOB ID: R-218637 ADDITIONAL LOCATIONS: India - Hyderabad WORK LOCATION TYPE: On Site DATE POSTED: Jul. 08, 2025 CATEGORY: Safety Job Summary Responsible for performing adverse event/product complaints correlation analysis and post market surveillance and perform literature and regulatory intelligence review. Prepare and provide metrics for management reviews, as well as data pulls and applicable sections for Global Periodic Aggregate Safety Reports, Device Periodic Safety Update Reports (PSUR), Medical Device Regulation (MDR) and Clinical Evaluation Reports (CER). Roles and Responsibilities Key Activities Working under the supervision of the Post Market Surveillance and Tre...

Job Title: Graphic Designer Location: On-site (Mohali) Experience: 4+ Years Employment Type: Full-Time Shift Timings - 8:30 PM -5:30 AM IST About SafeAeon SafeAeon is a trusted Managed Security Services Provider (MSSP), delivering 24/7 cybersecurity services including SOC, MDR, Email Security, and more. We are looking for a talented Graphic Designer to join our growing team and bring creative ideas to life through strong visuals that support our marketing and branding goals. Key Responsibilities Design digital creatives including social media posts, landing pages, web graphics, ads, infographics, whitepapers, and presentations. Work closely with the marketing and technical teams to align vis...

About Paytm Group: Paytm is India's leading mobile payments and financial services distribution company. Pioneer of the mobile QR payments revolution in India, Paytm builds technologies that help small businesses with payments and commerce. Paytm’s mission is to serve half a billion Indians and bring them to the mainstream economy with the help of technology. About the Role As a Product Manager for Card Acquiring , you will be responsible for building and scaling card-based payment products for our vast network of offline and online merchants. You will work closely with banks, networks (Visa, Mastercard, Rupay, American Express), and internal teams to deliver high-performance card processing...

As a Product Assessor, you will play a crucial role in our organization by overseeing Sterilization product assessments and conducting technical file reviews in strict adherence to regulatory requirements, including the European Medical Device Directive and Medical Device Regulation for Class IIa/IIb and/or Class III. Your primary focus will be to ensure the technical soundness of reviews and compliance with all relevant standards. Responsibilities: Conduct comprehensive Sterilization product assessments in line with regulatory requirements for medical devices. Support CE marking activities conducted by SGS, contributing to the overall certification process. Effectively communicate with coll...

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 We help progressive enterprises navigate the new reality of digital risks with proactive and intelligent cybersecurity. Job Description Cybersecurity Intern - Trainee SOC Analyst Are you ready to be on the frontline of cyber defense? We are seeking a dedicated and ambitious Cybersecurity Intern to join our Managed Detection & Response (MDR) team. Dive into the heart of action where every day presents a new challenge, and your strategic decisions have real-world impact. This internship offers a unique opportunity to gain hands-on experience in cybersecurity, working alongside experienced analysts to protect our client assets and infrastructure. Requirements Key Responsibilities: Moni...

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-...

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Analyst Qualifications: Master of Pharmacy Years of Experience: 3 to 5 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be aligned with our Life Science...

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 Team Lead – Medical Devices Location: Chennai, India Department: Regulatory Affairs Experience Required: Minimum 5 years Reports To: Head of Regulatory Affairs / Director of Quality & Regulatory Job Summary: We are seeking a highly skilled and experienced Senior Regulatory Affairs Team Lead to manage and lead our regulatory submissions and strategy for medical devices in India. The ideal candidate will have a deep understanding of the regulatory framework governed by CDSCO (Central Drugs Standard Control Organization) and proven experience in successfully obtaining approvals for medical devices. This role requires both strategic oversight and hands-on exe...

Duties and Responsibilities:  Responsible for strategic development, implementation, maintenance, and overall success of the company’s regulatory project approvals in different countries.  Develop, implement, and support a comprehensive regulatory compliance strategy to meet global market requirements for our products and ensure alignment with our overall business strategy.  Regulatory affairs strategy and coordination with Internal and external team for Asia, Africa, ANZ, Middle East, Europe and LATAM countries.  Coordinate with the Sales & Marketing team for business continuity and center of contact for all regulatory matters.  Global coordination for regulatory planning and execu...

Education: Bachelor’s degree in Mechanical , Automobile , or Polymer Science or Diploma in the same fields Experience: Minimum 10 years in quality control , preferably in rubber or rubber-to-metal bonded product industries Experience with railway component standards (RDSO, CLW, ICF, RCF) is highly desirable Core Responsibilities: Independent Quality Leadership Lead the quality control function independently— separate from daily production and testing Oversee product validation, failure analysis , and corrective action planning Quality Management System Ensure implementation and continual improvement of the QMS as per ISO 9001 , IRIS , RDSO Collaborate with Design & R&D for new product develo...

Education: Bachelor’s degree in Rubber Technology, Polymer Science, or Chemical Engineering or Diploma in the above fields Experience: 5+ years for degree holders 10+ years for diploma holders Experience in rubber product manufacturing (preferably for railway or automotive sectors) Technical Responsibilities: Apply expertise in rubber chemistry, compounding, and formulation design Operate and interpret results from key equipment: 1) Kneaders, mixing mills, hydraulic/injection presses 2) Rheometers (MDR/ODR), Mooney viscometers 3) TGA, DSC, FTIR analyzers Analyze and interpret: 1) Rheographs 2) Thermo-analytical curves 3) FTIR spectra and physical property charts Develop, optimize, and valida...

Location: Sanand, Ahmedabad Experience: 7+ years Global Markets: Asia, Africa, ANZ, Europe, Middle East, LATAM 🔧 Key Responsibilities: Lead global regulatory strategy, planning, and execution for product approvals Manage medical device registrations across multiple international markets Coordinate with cross-functional teams (Sales, Marketing, RA coordinators) Oversee post-approval changes, document control, and inspection readiness Ensure compliance with global standards: ISO 13485, MDSAP, EU MDR, 510(k), Indian MDR Maintain and update RA policies, labels, IFUs, translations, and marketing claims Train and lead a team of international RA professionals Act as point of contact for global regu...

Job Title : Regulatory Specialist (ISO, CE, BIS Certifications & Audits) Job Summary : A Regulatory Specialist focusing on ISO, CE, BIS certifications, and audits plays a critical role in ensuring that products, services, and processes adhere to international standards and regulatory requirements. This specialist works with cross-functional teams to facilitate the certification process, manage audits, and ensure ongoing compliance with certification bodies. They ensure that the company meets regulatory requirements, helping maintain or achieve certifications in various industries such as manufacturing, healthcare, electronics, and more. Key Responsibilities :1. ISO Certification Management :...

About Paytm Group: Paytm is India's leading mobile payments and financial services distribution company. Pioneer of the mobile QR payments revolution in India, Paytm builds technologies that help small businesses with payments and commerce. Paytm’s mission is to serve half a billion Indians and bring them to the mainstream economy with the help of technology. About the Role As a Product Manager for Card Acquiring , you will be responsible for building and scaling card-based payment products for our vast network of offline and online merchants. You will work closely with banks, networks (Visa, Mastercard, Rupay, American Express), and internal teams to deliver high-performance card processing...

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 Review new and modified product design documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and product requirements. Capable of mentoring junior quality engineers in providing quality engineering support. Responsibilities may include the following and other duties may be assigned Review New Product Introduction (NPI) and Released Product Management (Released Products) docume...

About Paytm Group: Paytm is India's leading mobile payments and financial services distribution company. Pioneer of the mobile QR payments revolution in India, Paytm builds technologies that help small businesses with payments and commerce. Paytm’s mission is to serve half a billion Indians and bring them to the mainstream economy with the help of technology. About the Role As a Product Manager for Card Acquiring , you will be responsible for building and scaling card-based payment products for our vast network of offline and online merchants. You will work closely with banks, networks (Visa, Mastercard, Rupay, American Express), and internal teams to deliver high-performance card processing...

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. Preference will be given to candidates who can join immediately or short notice. What you will do, Handle client engagements and work as the main point of contact for MDR projects Continuously improve client engagement and the quality of delivery to SOC customers. Implement standards and procedures for projects to ensure alerts are addressed with relevancy, accuracy and in a timely manner Define process and m...

Job Purpose: To ensure effective and timely management of product complaints by receiving, documenting, investigating, analyzing, and resolving product-related complaints in compliance with applicable regulatory requirements (e.g., ISO 13485, FDA 21 CFR Part 820, MDR). The role supports continuous improvement of product quality and customer satisfaction. Key Responsibilities: Receive and log product complaints from customers, sales team, or regulatory bodies in the complaint management system. Acknowledge receipt of complaints and communicate resolution timelines to complainants. Evaluate the complaint to determine if it qualifies as a reportable event per regulatory requirements. Coordinate...

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...