606 Mdr Jobs - Page 8

Position - CyberSecurity Team Lead Experience - 5-7 yr Budget -13-15 LPA Location - Chennai Working Mode - On-site Primary Skills - SOC, Cybersecurity, Team Lead, one cybersecurity certification (e.g., CEH, CySA+), technical documentation Preferred / Advantageous Skills- Managed Security Services Provider (MSSP), SIEM engineering,Exposure to cloud security incidents Key Responsibilities Act as the primary point of contact for MDR client engagements and ensure smooth project execution. Drive implementation of emerging threat intelligence (IOCs, detection rules, etc.) to identify affected systems and assess attack scope. Develop, document, and maintain SOC processes, standards, and alert triage procedures to ensure effective and timely response. Define and mature playbooks for cyber threat response operations. Autonomously conduct investigations and escalate incidents per defined protocols. Mentor, guide, and lead SOC analysts to foster a high-performance incident response team. Lead SOC operations during active cyber incidents and coordinate with executive leadership. Develop and maintain SOC dashboards and reporting metrics for performance and threat monitoring. Organize and conduct cybersecurity tabletop exercises and attack simulations. What We Look For 7+ years of experience in Security Operations Center (SOC) or a similar role (experience in MSSP environments is a plus). Bachelor's degree in Computer Science , Information Technology , or Cybersecurity . Industry certifications such as CySA+ , CEH , CSA , ECIH , or Cloud Security certifications. Proven experience managing SOC daily operations and incident response frameworks. Strong technical writing and documentation skills. Demonstrated leadership in guiding high-performing technical teams. Excellent communication skills, with the ability to collaborate cross-functionally and present to stakeholders. Hands-on experience with cloud security incidents and SIEM engineering is a strong advantage. A commitment to continuous learning and skill development in the cybersecurity field.

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 Trending Lead, the Combination Product & Medical Device Safety Vigilance Specialist will be responsible for: Regulatory Intelligence Review Review Regulatory updates from GPS PV Intelligence for impact to Combination Product Safety (CPS). Literature Review Perform the review of literature search results for the applicable devices. Post-Product Risk Periodic Review Pull data from database review AEs and evaluate any changes to P2 values. External Safety Data Review Pull data from MAUDE (FDA Manufacturer and User facility device experience) and FAERs database. Product Complaint (PC) Trending Correlation with Adverse Events (AE) Evaluate AEs co-reported with PC excursions identified from monthly PC holistic review to assess impact to patient and user safety (i.e., safety concerns or new harms). Reconcile AE lot excursions with PC lot excursions to support PC trending deep dives Post-marketing Surveillance of Combination Products and Medical Devices Pull data to support post marketing surveillance activities for combination products and medical devices. Metrics Pull, analyze and provide metrics for various governance forums. Support audits and inspections, as appropriate. Required Knowledge and Skills: Safety experience in biotech or pharmaceutical industry. Complaints or complaints trending within a development, manufacturing, or post-market environment. Knowledge of product complaints and adverse events intake and processing process. Ability to pull and analyse product complaints and/or adverse events data per request. Knowledge of medical devices or combination products, including device safety monitoring regulations and standards. Very strong knowledge of post market safety reporting regulations for medical devices/combination products globally. Data querying skills and experience with data visualizations tools such as Tableau, Power BI, or Python. Excellent interpersonal and teamwork skills. Critical scientific thinking and problem solving with attention to detail. Working knowledge of Microsoft Suite (Outlook, Word, Excel, PowerPoint). Preferred Knowledge and Skills: Knowledge of combination products and medical devices, including device safety monitoring regulations and standards. Ability to perform data analysis and derive insights. Organizational savvy and ability to operate effectively in a matrix environment. Prioritization and time management skills. Basic Qualifications: Doctorate degree and 8+ years of Post market surveillance and data analysis experience OR Master’s degree or Bachelor’s degree and 9+ years of Post market surveillance and data analysis experience

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 Market Surveillance and EU MDR requirements include but are not limited to identifying strategic focus areas for continuous improvements, product/process enhancements, implementing proactive quality activities, monitoring, and measuring the overall performance, and ensuring compliance to quality systems and regulatory requirements. Key Responsibilities include : Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis Risk management –Risk assessment. Propose strategies and solutions to data issues or challenges that occur during the PSUR writing and conclusion process. Skill Set: Proficient in post market surveillance regulations, specifically EU MDR. Hands on experience of Risk Management process as per ISO 14971 Sound knowledge on complaint trending Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Applied understanding of GDP, ISO 9001 & ISO 13485, FDA 21CFR Part 822 / 820 Additional: Effective interpersonal communications & Excellent analytical skills. Demonstrated organizational and written/verbal communication skills. Drive self-initiative to improve process Ability to work independently and in a team environment Desired Profile Education B. Tech / B.E in a field related to the life sciences or a relevant medical engineering field (biology, physiology, biomaterials, biomedical engineering or similar). Experience: 2 to 4 years of experience in Scientific or Medical Writing, and/or Quality and regulatory experience in post market surveillance. Experience with medical device, orthopedic or trauma devices preferred Personality: Proactive, independent, team player with a strong service mentality. You are characterized by analytical and transdisciplinary reasoning, with a good attention to detail. You value an international working environment, working across sites and indications. Job Type: Full-time Pay: ₹56,000.00 - ₹67,000.00 per month Work Location: In person

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 Market Surveillance and EU MDR requirements include but are not limited to identifying strategic focus areas for continuous improvements, product/process enhancements, implementing proactive quality activities, monitoring, and measuring the overall performance, and ensuring compliance to quality systems and regulatory requirements. Key Responsibilities include : Create PMS plan, PMS report, PSUR report as per EUMDR, Trend report & Complaint analysis Risk management –Risk assessment. Propose strategies and solutions to data issues or challenges that occur during the PSUR writing and conclusion process. Skill Set: Proficient in post market surveillance regulations, specifically EU MDR. Hands on experience of Risk Management process as per ISO 14971 Sound knowledge on complaint trending Demonstrated ability to work effectively with various work groups to assure conformance to regulatory requirements, internal processes, and policies. Demonstrated ability to self-motivate, ability to prioritize tasks in a deadline-driven environment. Demonstrated ability to effectively work with others in various coordinate disciplines and on multi-national teams. Applied understanding of GDP, ISO 9001 & ISO 13485, FDA 21CFR Part 822 / 820 Additional: Effective interpersonal communications & Excellent analytical skills. Demonstrated organizational and written/verbal communication skills. Drive self-initiative to improve process Ability to work independently and in a team environment Desired Profile Education B. Tech / B.E in a field related to the life sciences or a relevant medical engineering field (biology, physiology, biomaterials, biomedical engineering or similar). Experience: 2 to 4 years of experience in Scientific or Medical Writing, and/or Quality and regulatory experience in post market surveillance. Experience with medical device, orthopedic or trauma devices preferred Personality: Proactive, independent, team player with a strong service mentality. You are characterized by analytical and transdisciplinary reasoning, with a good attention to detail. You value an international working environment, working across sites and indications. Job Type: Full-time Pay: ₹58,000.00 - ₹67,000.00 per month Work Location: In person

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, 21 CFR part 11, EUMDR and product specific industry standards. Good verbal and written communication skills including plan / report development. Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485, and the Medical Device Regulation. Collaborate with cross-functional teams to gather and analyze data related to the performance and safety of medical devices and independently develop Periodic safety update plan and reports. Partner with regulatory affairs and medical experts to ensure accurate and timely submission of PSURs to regulatory authorities. Continuously monitor and stay updated with evolving safety regulations and guidelines to ensure PSUR compliance. Familiar with Literature review, PMCF, IMDRF coding, CAPA and NCMR. Hands on experience in signal evaluation trending and reports, preliminary code reviews for the product complaints on periodic basis. Develop templates and trainings based on the quality system regulations, applicable standards and guidance. Independently review all deliverables to ensure compliance with development process and the standard. Deliver presentations to the QA organization on status and issues of assigned projects. Deliver trainings to departments outside of QA. Demonstrates ability to effectively play multiple roles on a cross-functional team including contributor, subject matter expert, leader, facilitator. Hands-on experience on EU MDR. Previous experience working in a cross-functional team environment. Hands-on experience on Risk Management, Design Controls for Medical Devices. Participate when appropriate in audits. Experience in collaborating with regulatory affairs teams for submission of safety reports. Required Knowledge and Experience Minimum 5-8 years of quality engineering experience or equivalence and overall 8-12 years of experience. Understanding of post-market surveillance processes and adverse event reporting. Knowledge of risk management principles and hazard analysis in the context of medical devices. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

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 Trending Lead, the Combination Product & Medical Device Safety Vigilance Specialist will be responsible for: Regulatory Intelligence Review Review Regulatory updates from GPS PV Intelligence for impact to Combination Product Safety (CPS). Literature Review Perform the review of literature search results for the applicable devices. Post-Product Risk Periodic Review Pull data from database review AEs and evaluate any changes to P2 values. External Safety Data Review Pull data from MAUDE (FDA Manufacturer and User facility device experience) and FAERs database. Product Complaint (PC) Trending Correlation with Adverse Events (AE) Evaluate AEs co-reported with PC excursions identified from monthly PC holistic review to assess impact to patient and user safety (i.e., safety concerns or new harms). Reconcile AE lot excursions with PC lot excursions to support PC trending deep dives Post-marketing Surveillance of Combination Products and Medical Devices Pull data to support post marketing surveillance activities for combination products and medical devices. Metrics Pull, analyze and provide metrics for various governance forums. Support audits and inspections, as appropriate. Required Knowledge and Skills: Safety experience in biotech or pharmaceutical industry. Complaints or complaints trending within a development, manufacturing, or post-market environment. Knowledge of product complaints and adverse events intake and processing process. Ability to pull and analyse product complaints and/or adverse events data per request. Knowledge of medical devices or combination products, including device safety monitoring regulations and standards. Very strong knowledge of post market safety reporting regulations for medical devices/combination products globally. Data querying skills and experience with data visualizations tools such as Tableau, Power BI, or Python. Excellent interpersonal and teamwork skills. Critical scientific thinking and problem solving with attention to detail. Working knowledge of Microsoft Suite (Outlook, Word, Excel, PowerPoint). Preferred Knowledge and Skills: Knowledge of combination products and medical devices, including device safety monitoring regulations and standards. Ability to perform data analysis and derive insights. Organizational savvy and ability to operate effectively in a matrix environment. Prioritization and time management skills. Basic Qualifications: Doctorate degree and 8+ years of Post market surveillance and data analysis experience OR Master’s degree or Bachelor’s degree and 9+ years of Post market surveillance and data analysis experience

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 visuals with campaign objectives. Create motion graphics and short-form animations for video content. Independently research, curate, and develop fresh, brand-consistent design ideas. Stay up to date and experiment with the latest AI-powered design tools to improve output and creativity. Adapt visual assets for different platforms like LinkedIn, YouTube, websites, and emailers. Ensure all materials follow brand guidelines and maintain visual consistency across campaigns. Required Skills & Experience Minimum 4 years of hands-on experience as a Graphic Designer. Strong experience working in the IT industry and/or advertising agency setup is required. Experience in the cybersecurity industry is a plus. Proficiency in Adobe Creative Suite (Photoshop, Illustrator, InDesign, After Effects, Premiere Pro). Familiarity with tools like Canva, Figma, CorelDRAW. Strong portfolio that reflects creativity in both static and motion design. Must be proactive, self-managed, and capable of handling end-to-end design tasks independently. Preferred Skills Working knowledge of AI tools such as Midjourney, Adobe Firefly, RunwayML, or similar. Understanding of basic UI/UX principles. Knowledge of HTML/CSS is a plus but not required. Why Join SafeAeon? Opportunity to work with a global leader in cybersecurity services. Collaborate on high-impact campaigns with creative freedom. Exposure to modern tools and fast-growing technologies. Competitive compensation and career growth support. To Apply: Send your resume and design portfolio to recruitment@safeaeon.com Subject line: Graphic Designer – Application – [Your Name] Job Type: Full-time Pay: ₹30,000.00 - ₹55,000.00 per month Benefits: Health insurance Provident Fund Schedule: Monday to Friday Night shift Shift availability: Night Shift (Required) Work Location: In person

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 solutions. You will be the voice of the merchant and the architect of high-SR, low-latency, and regulation-compliant card payment infrastructure. Ke y Responsibilities:- Own the end-to-end lifecycle of card acquiring products – from strategy and roadmap to execution and post-launch performance. Define product features and enhancements focused on card payment acceptance across POS, online, and in-app channels. Integrate and manage partnerships with issuer and acquirer banks, card networks, and processors. Monitor and drive improvements in key metrics such as transaction success rate (SR), latency, authorization rates, fraud, and chargebacks. Lead initiatives related to card tokenization, contactless/NFC enablement, recurring payments (SI on cards), and international acceptance. Collaborate with engineering, design, risk, legal, and compliance to ensure scalable and compliant rollout of features. Track RBI regulations, network advisories, and ensure product readiness and compliance. Work with sales and operations teams to enable adoption and resolution of merchant issues. What You’ll Need 4–8 years of product management experience, with at least 2 years in card payments, acquiring, or processing. Strong understanding of card acquiring infrastructure, transaction lifecycle, settlement, MDR, and risk/fraud handling. Experience in working with card networks (Visa, Mastercard, Rupay), acquiring banks, or payment processors. Data-driven decision-making with hands-on experience in SQL, Excel, or dashboarding tools. Excellent stakeholder management, cross-functional collaboration, and problem-solving skills. Familiarity with RBI and PCI-DSS compliance standards is a plus. Why Join Us Be a key player in shaping the card payments experience for millions of Indian merchants. Solve for scale: Handle transaction volumes at one of the largest payment processors in India. Work with some of the most talented teams across product, engineering, and design. Join a fast-paced, impact-driven environment with a focus on innovation, ownership, and excellence. Compensation : If you are the right fit, we believe in creating wealth for you With enviable 500 mn+ registered users, 17 mn+ merchants and depth of data in our ecosystem, we are in a unique position to democratize credit for deserving consumers & merchants – and we are committed to it. India’s largest digital lending story is brewing here. It’s your opportunity to be a part of the story!

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 colleagues and clients regarding product assessments and related activities. Work proactively to minimize risks associated with medical device certifications. A degree or equivalent qualification with Microbiology modules or relevant studies (e.g., medicine, pharmacy, engineering, or other related sciences). Four years industrial experience with medical device manufacturing that includes a

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-leading Taegis XDR/MDR, identity threat detection and response (ITDR), next-gen SIEM capabilities, managed risk, and a comprehensive set of advisory services. Sophos sells all these solutions through reseller partners, Managed Service Providers (MSPs) and Managed Security Service Providers (MSSPs) worldwide, defending more than 600,000 organizations worldwide from phishing, ransomware, data theft, other every day and state-sponsored cybercrimes. The solutions are powered by historical and real-time threat intelligence from Sophos X-Ops and the newly added Counter Threat Unit (CTU). Sophos is headquartered in Oxford, U.K. More information is available at www.sophos.com. Role Summary Working as part of the Global Service Desk Team this role will have specific responsibility for the effective management and improvement of the Incident Management, Service Request Processes, enchantments & documenting the new or existing SOP to provide faster & better IT support to all Sophos Department. What you will do Provide IT Support to Sophos employees by triaging the Incident, Request, and call Support PC hardware components, desktop operating system software, and application software Perform standard Image Deployment process Perform repairs to equipment and arrange for other servicing needs Provide escalated technical support. Identify and report system issues to vendors. Monitor and test resolution of those issues sent to vendors. Communicating with vendor for warranty claims Perform Asset Check and Inventory Working with Asset Manager, maintain suitable regional stock levels of IT equipment by raising quotes and orders with chosen vendors to fulfill the stock needs. Contribute to Sophos Technical Documentation and can provide user training for basic hardware and software use Provides reports to immediate superior on daily tasks and activities Performs other functions and requests assigned by immediate superior Ensure high-quality customer service What you will bring 2-6 years of experience in IT or service desk roles Strong knowledge on different Operating System (Win10, MacOS, Linux) Knowledge on Azure, O365, Active Directory, IAM Tool (prefer Saviynt), JAMF Must be available and willing to commit to the working hours and responsibilities associated with the role Must be a graduate level degree and above in a Information Technology field Understanding of Operating system, computer hardware, networking equipment and print services Ability to prioritize tasks and efficiently manage time Good oral and written communications skills Ability to respond effectively to inquiries or complaints Ability to develop, maintain, and promote strong internal and external relationships Strong problem solving and analytical skills Basic networking knowledge (DNS, DHCP, VPN, Wi-Fi) #B1 Ready to Join Us? At Sophos, we believe in the power of diverse perspectives to fuel innovation. Research shows that candidates sometimes hesitate to apply if they don't check every box in a job description. We challenge that notion. Your unique experiences and skills might be exactly what we need to enhance our team. Don't let a checklist hold you back – we encourage you to apply. What's Great About Sophos? · Sophos operates a remote-first working model, making remote work the primary option for most employees. However, some roles may necessitate a hybrid approach. Please refer to the location details in our job postings for further information. · Our people – we innovate and create, all of which are accompanied by a great sense of fun and team spirit · Employee-led diversity and inclusion networks that build community and provide education and advocacy · Annual charity and fundraising initiatives and volunteer days for employees to support local communities · Global employee sustainability initiatives to reduce our environmental footprint · Global fitness and trivia competitions to keep our bodies and minds sharp · Global wellbeing days for employees to relax and recharge · Monthly wellbeing webinars and training to support employee health and wellbeing Our Commitment To You We’re proud of the diverse and inclusive environment we have at Sophos, and we’re committed to ensuring equality of opportunity. We believe that diversity, combined with excellence, builds a better Sophos, so we encourage applicants who can contribute to the diversity of our team. All applicants will be treated in a fair and equal manner and in accordance with the law regardless of gender, sex, gender reassignment, marital status, race, religion or belief, color, age, military veteran status, disability, pregnancy, maternity or sexual orientation. We want to give you every opportunity to show us your best self, so if there are any adjustments we could make to the recruitment and selection process to support you, please let us know. Data Protection If you choose to explore an opportunity, and subsequently share your CV or other personal details with Sophos, these details will be held by Sophos for 12 months in accordance with our Privacy Policy and used by our recruitment team to contact you regarding this or other relevant opportunities at Sophos. If you would like Sophos to delete or update your details at any time, please follow the steps set out in the Privacy Policy describing your individual rights. For more information on Sophos’ data protection practices, please consult our Privacy Policy Cybersecurity as a Service Delivered | Sophos

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-leading Taegis XDR/MDR, identity threat detection and response (ITDR), next-gen SIEM capabilities, managed risk, and a comprehensive set of advisory services. Sophos sells all these solutions through reseller partners, Managed Service Providers (MSPs) and Managed Security Service Providers (MSSPs) worldwide, defending more than 600,000 organizations worldwide from phishing, ransomware, data theft, other every day and state-sponsored cybercrimes. The solutions are powered by historical and real-time threat intelligence from Sophos X-Ops and the newly added Counter Threat Unit (CTU). Sophos is headquartered in Oxford, U.K. More information is available at www.sophos.com. Role Summary Working as part of the Global Service Desk Team this role will have specific responsibility for the effective management and improvement of the Incident Management, Service Request Processes, enchantments & documenting the new or existing SOP to provide faster & better IT support to all Sophos Department. What you will do Provide IT Support to Sophos employees by triaging the Incident, Request, and call Support PC hardware components, desktop operating system software, and application software Perform standard Image Deployment process Perform repairs to equipment and arrange for other servicing needs Provide escalated technical support. Identify and report system issues to vendors. Monitor and test resolution of those issues sent to vendors. Communicating with vendor for warranty claims Perform Asset Check and Inventory Working with Asset Manager, maintain suitable regional stock levels of IT equipment by raising quotes and orders with chosen vendors to fulfill the stock needs. Contribute to Sophos Technical Documentation and can provide user training for basic hardware and software use Provides reports to immediate superior on daily tasks and activities Performs other functions and requests assigned by immediate superior Ensure high-quality customer service What you will bring 2-6 years of experience in IT or service desk roles Strong knowledge on different Operating System (Win10, MacOS, Linux) Knowledge on Azure, O365, Active Directory, IAM Tool (prefer Saviynt), JAMF Must be available and willing to commit to the working hours and responsibilities associated with the role Must be a graduate level degree and above in a Information Technology field Understanding of Operating system, computer hardware, networking equipment and print services Ability to prioritize tasks and efficiently manage time Good oral and written communications skills Ability to respond effectively to inquiries or complaints Ability to develop, maintain, and promote strong internal and external relationships Strong problem solving and analytical skills Basic networking knowledge (DNS, DHCP, VPN, Wi-Fi) #B1 Ready to Join Us? At Sophos, we believe in the power of diverse perspectives to fuel innovation. Research shows that candidates sometimes hesitate to apply if they don't check every box in a job description. We challenge that notion. Your unique experiences and skills might be exactly what we need to enhance our team. Don't let a checklist hold you back – we encourage you to apply. What's Great About Sophos? · Sophos operates a remote-first working model, making remote work the primary option for most employees. However, some roles may necessitate a hybrid approach. Please refer to the location details in our job postings for further information. · Our people – we innovate and create, all of which are accompanied by a great sense of fun and team spirit · Employee-led diversity and inclusion networks that build community and provide education and advocacy · Annual charity and fundraising initiatives and volunteer days for employees to support local communities · Global employee sustainability initiatives to reduce our environmental footprint · Global fitness and trivia competitions to keep our bodies and minds sharp · Global wellbeing days for employees to relax and recharge · Monthly wellbeing webinars and training to support employee health and wellbeing Our Commitment To You We’re proud of the diverse and inclusive environment we have at Sophos, and we’re committed to ensuring equality of opportunity. We believe that diversity, combined with excellence, builds a better Sophos, so we encourage applicants who can contribute to the diversity of our team. All applicants will be treated in a fair and equal manner and in accordance with the law regardless of gender, sex, gender reassignment, marital status, race, religion or belief, color, age, military veteran status, disability, pregnancy, maternity or sexual orientation. We want to give you every opportunity to show us your best self, so if there are any adjustments we could make to the recruitment and selection process to support you, please let us know. Data Protection If you choose to explore an opportunity, and subsequently share your CV or other personal details with Sophos, these details will be held by Sophos for 12 months in accordance with our Privacy Policy and used by our recruitment team to contact you regarding this or other relevant opportunities at Sophos. If you would like Sophos to delete or update your details at any time, please follow the steps set out in the Privacy Policy describing your individual rights. For more information on Sophos’ data protection practices, please consult our Privacy Policy Cybersecurity as a Service Delivered | Sophos

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: Monitor Security Alerts: Assist in monitoring and analyzing security alerts from various sources to identify potential threats. Incident Response: Participate in incident response activities, including investigation, containment, and remediation of security incidents. Log Analysis: Analyze system logs to detect suspicious activities and potential security breaches. Threat Intelligence: Assist in gathering and analyzing threat intelligence to stay updated on the latest cybersecurity threats and trends. Vulnerability Management: Support the team in identifying and mitigating vulnerabilities in systems and applications. Security Tools: Gain hands-on experience with security tools such as SIEM (Security Information and Event Management), firewalls, and intrusion detection/prevention systems. Documentation: Prepare detailed reports on security incidents, findings, and recommendations for improvement. Qualifications Fresh graduate with a degree in Cybersecurity, Computer Science, Information Technology, or a related field (Final year undergraduates who are completing their studies in few months will also be considered) Basic understanding of cybersecurity concepts and principles. Familiarity with operating systems (Windows, Linux) and networking fundamentals. Strong analytical and problem-solving skills. Excellent communication skills, both verbal and written. Ability to work independently and as part of a team. Eagerness to learn and stay updated on the latest cybersecurity trends and technologies. Learning Objectives Develop a deep understanding of SOC operations and cybersecurity practices. Gain practical experience in incident response and threat analysis. Enhance skills in log analysis, vulnerability management, and security tool usage. Build a foundation for a career in cybersecurity. check(event) ; career-website-detail-template-2 => apply(record.id,meta)" mousedown="lyte-button => check(event)" final-style="background-color:#1D2354;border-color:#1D2354;color:white;" final-class="lyte-button lyteBackgroundColorBtn lyteSuccess" lyte-rendered="">

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-hoc changes in priority/planning and independently. Be able to think from customer expectation perspective Be able to work in different teams simultaneously Communicative & disciplined team worker

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 Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services. Employees under this span will be a part of one of the sub-offerings - Regulatory, helping the worlds leading biopharma companies bring their vision to life enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The incumbent will perform the regulatory affairs tasks of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components. Veeva Regulatory Suite experienceCollect, collate and evaluate the scientific data gathered as part of R & D. Advise on legal and scientific restraints and requirements. Ensure the organization`s products comply with current regulations. Example; Build regulatory submission strategy, author CMC documents, and health authority packages etc. What are we looking for Life Sciences Regulatory ServicesAbility to handle disputesAbility to manage multiple stakeholdersAbility to meet deadlinesAbility to perform under pressureAbility to work well in a teamLife Sciences Automation Enablement Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualification Master of Pharmacy

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-leading Taegis XDR/MDR, identity threat detection and response (ITDR), next-gen SIEM capabilities, managed risk, and a comprehensive set of advisory services. Sophos sells all these solutions through reseller partners, Managed Service Providers (MSPs) and Managed Security Service Providers (MSSPs) worldwide, defending more than 600,000 organizations worldwide from phishing, ransomware, data theft, other every day and state-sponsored cybercrimes. The solutions are powered by historical and real-time threat intelligence from Sophos X-Ops and the newly added Counter Threat Unit (CTU). Sophos is headquartered in Oxford, U.K. More information is available at www.sophos.com. Role Summary Sophos engineers are working on cloud based next generation management, reporting and telemetry solutions of the Sophos security products using microservices architecture. As a member of the development team, you will work on prototyping new cloud solutions as well as build the production ready complete cloud solutions. We are looking for smart Cloud Developers with solid experience into microservices architecture on AWS, having an innovative mindset and with a blend of scripting, developing, and testing skills with exposure to DevOps process. The most suitable candidate would be one having a combination of working experience in both cloud/AWS and managed switch/routers/firewall technology. What you will do Design and develop cloud based next generation management, reporting and telemetry solutions of the Sophos security products using micro services architecture Work on prototyping new cloud solutions as well as build the production ready complete cloud solutions Own and drive to resolution any escalations on product Running test automation scripts to verify issues and fixes What you will bring 15+ years of work experience in relevant domain and discipline 4+ years of hands-on experience as a Principal-level software engineer Solid understanding of Amazon AWS Cloud infrastructure & microservices development Prior experience in operations of workloads on AWS using Amazon Elastic Kubernetes Service (Amazon EKS), Amazon Elastic Container Service (ECS), Kubernetes or others Solid understanding of highly-available and fault-tolerant enterprise and web-scale software deployments Be able to write “infra as code” using Terraform Strong problem-solving skills Working knowledge of as many of the following tools: Languages: Java (C or Go experience is a plus) Scripting: Python, JavaScript, Bash DevOps and build: Jenkins, Git, Gradle, GitHub Actions Containers: Docker, Docker swarm, Kubernetes cluster OS: Linux/Unix Ability to work both independently and in a team environment Demonstrate passion, desire, and dedication to ongoing learning Proactive, flexible attitude to work with a willingness to constantly review and improve skills and processes Bachelor’s of Science in Computer Software, Computer Science or related discipline or equivalent experience Proven ability to work independently across teams and actively contribute to architecture reviews at the Business Unit (BU) level Experience on managed switch, routers and Firewall technology, C, C++, Linux Master’s of Science in Computer software, Computer Science or related discipline #B2 Ready to Join Us? At Sophos, we believe in the power of diverse perspectives to fuel innovation. Research shows that candidates sometimes hesitate to apply if they don't check every box in a job description. We challenge that notion. Your unique experiences and skills might be exactly what we need to enhance our team. Don't let a checklist hold you back – we encourage you to apply. What's Great About Sophos? · Sophos operates a remote-first working model, making remote work the primary option for most employees. However, some roles may necessitate a hybrid approach. Please refer to the location details in our job postings for further information. · Our people – we innovate and create, all of which are accompanied by a great sense of fun and team spirit · Employee-led diversity and inclusion networks that build community and provide education and advocacy · Annual charity and fundraising initiatives and volunteer days for employees to support local communities · Global employee sustainability initiatives to reduce our environmental footprint · Global fitness and trivia competitions to keep our bodies and minds sharp · Global wellbeing days for employees to relax and recharge · Monthly wellbeing webinars and training to support employee health and wellbeing Our Commitment To You We’re proud of the diverse and inclusive environment we have at Sophos, and we’re committed to ensuring equality of opportunity. We believe that diversity, combined with excellence, builds a better Sophos, so we encourage applicants who can contribute to the diversity of our team. All applicants will be treated in a fair and equal manner and in accordance with the law regardless of gender, sex, gender reassignment, marital status, race, religion or belief, color, age, military veteran status, disability, pregnancy, maternity or sexual orientation. We want to give you every opportunity to show us your best self, so if there are any adjustments we could make to the recruitment and selection process to support you, please let us know. Data Protection If you choose to explore an opportunity, and subsequently share your CV or other personal details with Sophos, these details will be held by Sophos for 12 months in accordance with our Privacy Policy and used by our recruitment team to contact you regarding this or other relevant opportunities at Sophos. If you would like Sophos to delete or update your details at any time, please follow the steps set out in the Privacy Policy describing your individual rights. For more information on Sophos’ data protection practices, please consult our Privacy Policy Cybersecurity as a Service Delivered | Sophos

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 execution, ensuring regulatory compliance and timely product registrations. Key Responsibilities: Lead Regulatory Submissions: Drive end-to-end regulatory submissions to CDSCO for new product approvals, including Class A, B, C, and D medical devices. Dossier Preparation: Oversee the compilation, review, and submission of Device Master Files (DMFs), Plant Master Files (PMFs), and other required documentation. Liaison with CDSCO: Serve as the primary point of contact with CDSCO officials, Notified Bodies, and authorized agents. Regulatory Strategy: Develop and implement regulatory strategies for both new and existing product lines, ensuring alignment with local and international regulatory standards. Team Leadership: Manage and mentor a team of regulatory associates/specialists; provide guidance on technical file preparation, regulatory pathways, and compliance. Audit Support: Participate in internal and external audits (CDSCO, ISO 13485, MDSAP), including responding to observations and ensuring closure of compliance gaps. Monitoring & Intelligence: Stay current with CDSCO regulations, guidance documents, and global regulatory trends; disseminate regulatory intelligence to internal teams. Cross-functional Collaboration: Work closely with R&D, QA, Marketing, and Supply Chain to ensure regulatory requirements are incorporated throughout the product lifecycle. Requirements: Education: Bachelor’s or Master’s degree in Pharmacy, Biomedical Engineering, Life Sciences, or a related field. Experience: Minimum 5 years of hands-on regulatory experience with medical device registrations in India, with a focus on CDSCO Class C & D devices preferred. Regulatory Knowledge: Strong understanding of the Indian Medical Device Rules (MDR), 2017 and CDSCO’s submission pathways (Form MD-14/15, MD-16/17, MD-9/10, etc.). Technical Skills: Experience preparing technical documentation (CE, 510(k), or other global dossiers is a plus). Soft Skills: Excellent communication, leadership, problem-solving, and project management skills. Certifications (preferred): RAC (Regulatory Affairs Certification), ISO 13485 knowledge, or equivalent certifications. Intrested candidates Please forward your Resume to Ph:-8110076949 Job Type: Full-time Pay: ₹50,000.00 - ₹75,000.00 per month Benefits: Food provided Provident Fund Schedule: Day shift Experience: total work: 5 years (Required) Work Location: In person

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 execution, for the development and market introduction of Biotek Products  Regulatory compliance and medical device registration in Asia, Africa, ANZ, Middle East, Europe and LATAM countries. Management of a team of RA coordinators for different countries.  Manage post approval changes in Global market for all Biotek products  Ensure that regulated processes and systems are always inspection ready.  Draft, review, edit, and maintain all departmental policies and procedures, including Post approval changes, regulatory review of order, label and IFU requirements, Language translation needs, Marketing claims etc.  Manage, train and guide the team members as and when required.  Willingness to undertake other reasonable tasks within the scope of the position as instructed by the supervisor. Education and Professional Experience: Bachelors or Masters in Pharma/Engineering/life sciences with minimum 9 years of extensive experience in medical device regulatory affairs, preferably in Implants. Skills & Abilities:  Strong experience hosting regulatory inspections and interacting with regulators, Consultants, Customer, sales persons  Strong understanding of global registration requirements and demonstrated track record of successful market access.  Highly experienced in setting up the Regulatory requirement compliances as per ISO 13485 and MDSAP and maintaining the same.  Experience on areas such as EU MDR, ISO 14971, 510(k) submissions, Indian MDR, and post market surveillance would be preferred.  Proven ability to create culture of accountability and ownership  Proven track record with establishing and maintaining strong internal and external partnerships.  Must be able to work effectively at all levels in the organization in a matrix environment and with external partners.  Must demonstrate excellent written and verbal communication skills in English and work well with diverse teams and stakeholders in multiple locations.  Must possess the ability to conform to shifting priorities, demands and timelines through analytical and problem-solving capabilities to meet deadlines and prioritize work on multiple projects.  Highly independent and self-motivated and integrates well within a team.  Proven project management skills  Excellent presentation skills.  Structured and results-oriented approach.  Strong time management skills.  Proficiency in MS Office programs. Job Types: Full-time, Permanent Pay: ₹2,000,000.00 - ₹2,200,000.00 per year Benefits: Food provided Health insurance Paid sick time Provident Fund Schedule: Day shift Rotational shift Weekend availability Supplemental Pay: Joining bonus Performance bonus Quarterly bonus Shift allowance Yearly bonus Work Location: In person

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 development, validation, and approval testing Inspection & Compliance Provide technical inputs on material specs, tolerances , and functional performance Handle RDSO / third-party inspections , ensuring compliance to drawings and control plans Approve dispatch only after full technical conformity is achieved Testing & Calibration Oversee calibration and functioning of all lab equipment: UTM, Mooney Viscometer, MDR, Hardness Tester Validate results for: tensile, adhesion, compression set, hardness, aging tests, etc. Documentation & Analysis Maintain inspection reports, test logs, NCR records, and CAPA documentation Present quality metrics during Management Review Meetings (MRM) Skills & Competencies Technical Expertise: Rubber product testing, QAP interpretation, drawing compliance Standards: ISO, IRIS, RDSO, ASTM, customer-specific specifications Analytical Tools: FMEA, SPC, Control Plans, MSA, CAPA Instrumentation: UTM, MDR/ODR, Mooney Viscometer, Hardness Tester, TGA, DSC Data & Reporting:Quality reporting, inspection logs, NCRs, validation documents Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Application Question(s): Current Salary: Expected Salary: Notice Period: Experience: Quality management: 5 years (Preferred) License/Certification: ISO 9001, IRIS Certificate (Required) Work Location: In person Expected Start Date: 15/08/2025

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 validate compound formulations for: Rubber-to-metal bonded components Railway parts (e.g., axle box bushes, sandwich mounts, bump stops) Standards & Compliance: Ensure technical documentation aligns with: IRIS, ISO 9001/14001/45001, IATF 16949, ASTM, RDSO specifications and drawing requirements Support QA in maintaining QAPs, control plans, and lab records Facilitate technical inputs during inspections and audits (RDSO, RITES, etc.) Skills & Competencies: Strong data interpretation and technical writing Experience in lab process validation and troubleshooting Team collaboration with Production, QA, and NPD departments Proficiency in software for data logging and lab reports (Excel, ERP, LIMS) Job Type: Full-time Pay: ₹20,000.00 - ₹35,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Yearly bonus Application Question(s): Current Salary: Expected Salary: Notice Period: Experience: Rubber technology: 10 years (Required) Work Location: In person Expected Start Date: 15/08/2025

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 regulatory matters and external partners 📩 Apply Now: Interested candidates can apply directly via LinkedIn or email your updated resume to Unitedind@uhr.co.in 📞 Contact Person: Ansuya Satish / Anjali Batheja 9824350317 / 9723300064 Ansuya@uhr.co.in / Unitedind@uhr.co.in

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 : Coordinate ISO Certification Process : Manage the process of obtaining and maintaining ISO certifications (e.g., ISO 9001, ISO 13485, ISO 14001) for relevant departments or products. Compliance Monitoring : Monitor the organization's compliance with ISO standards, ensuring continuous improvement and adherence to documented procedures. Documentation and Reporting : Prepare and maintain necessary documentation for ISO certification audits and re-certifications. 2. CE Marking (European Conformity) : CE Certification Process : Assist in obtaining and maintaining CE marking for products, ensuring that they meet European Union safety, health, and environmental requirements. Regulatory Guidance : Provide guidance on the European regulatory landscape and ensure that products comply with EU directives and standards, such as the Medical Device Regulation (MDR) or Low Voltage Directive (LVD). Submission to Notified Bodies : Prepare technical documentation and work with notified bodies to get products certified for CE marking. 3. BIS (Bureau of Indian Standards) Certification : Manage BIS Certification Process : Facilitate the process for obtaining BIS certification for products and services in compliance with Indian standards. Liaise with BIS : Act as the primary point of contact for communication with the Bureau of Indian Standards, including the submission of applications and documentation for certification. Stay Updated on BIS Guidelines : Keep the organization updated on new BIS regulations, standards, and revisions that impact product certification. 4. Audit Management : Conduct Internal Audits : Organize and conduct internal audits to evaluate compliance with ISO, CE, BIS, and other relevant standards. Coordinate External Audits : Facilitate and manage external audits conducted by certification bodies or regulatory agencies to assess the company's compliance with relevant standards. Corrective and Preventive Actions (CAPA) : Identify non-compliance or areas for improvement during audits, and implement corrective and preventive actions (CAPA) in collaboration with relevant departments. Prepare Audit Reports : Document audit findings, track audit results, and report on the effectiveness of corrective actions. 5. Regulatory Compliance & Documentation : Regulatory Documentation : Develop and maintain comprehensive compliance documentation, including certificates, audit reports, procedures, and quality manuals. Compliance Updates : Ensure that all regulatory documentation is updated in line with changing standards or regulations (ISO, CE, BIS, etc.). Legal and Industry Standards : Stay current with changes in international and national standards and regulations that may affect the company’s certifications. 6. Training and Support : Employee Training : Conduct training sessions for internal teams to ensure understanding of ISO, CE, BIS, and audit requirements, emphasizing the importance of compliance and documentation. Cross-Department Collaboration : Work with product development, manufacturing, quality control, and management teams to ensure that all stages of product development and production comply with regulatory standards. 7. Risk Management & Continuous Improvement : Risk Assessment : Identify potential regulatory risks and recommend strategies to mitigate risks related to non-compliance or certification failures. Continuous Improvement : Advocate for a culture of continuous improvement within the organization, supporting efforts to enhance product quality and compliance processes. Skills and Qualifications : Education : A bachelor’s degree in engineering, business, quality management, regulatory affairs, or a related field. Advanced certifications in regulatory affairs or quality management systems (e.g., Lead Auditor for ISO, ISO 9001, or ISO 13485 certification) are preferred. Experience : 3-5 years of experience in regulatory affairs, quality management, or certification processes, preferably in industries such as manufacturing, electronics, healthcare, or automotive. Proven track record of managing ISO, CE, and BIS certifications and coordinating audits. Knowledge : Expertise in ISO 9001, ISO 13485, ISO 14001, CE marking process, and BIS certification requirements. Understanding of international regulatory standards (e.g., EU, US FDA, BIS) and their impact on product development, manufacturing, and quality control. Familiarity with risk management principles and corrective action procedures. Technical Skills : Proficiency in using Microsoft Office Suite (Excel, Word, PowerPoint) and quality management systems (QMS) or regulatory software tools. Strong documentation and report-writing skills. Soft Skills : Strong attention to detail and organizational skills. Excellent communication skills for collaborating with internal teams and external regulatory bodies. Ability to manage multiple projects simultaneously and meet deadlines. Problem-solving mindset with the ability to identify and address regulatory compliance issues. Work Environment : Regulatory specialists typically work in office settings but may need to travel for audits, inspections, or meetings with regulatory bodies. Industries employing Regulatory Specialists in ISO, CE, and BIS certification roles include manufacturing, automotive, electronics, healthcare, pharmaceuticals, and consumer goods.

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 solutions. You will be the voice of the merchant and the architect of high-SR, low-latency, and regulation-compliant card payment infrastructure. Ke y Responsibilities:- Own the end-to-end lifecycle of card acquiring products – from strategy and roadmap to execution and post-launch performance. Define product features and enhancements focused on card payment acceptance across POS, online, and in-app channels. Integrate and manage partnerships with issuer and acquirer banks, card networks, and processors. Monitor and drive improvements in key metrics such as transaction success rate (SR), latency, authorization rates, fraud, and chargebacks. Lead initiatives related to card tokenization, contactless/NFC enablement, recurring payments (SI on cards), and international acceptance. Collaborate with engineering, design, risk, legal, and compliance to ensure scalable and compliant rollout of features. Track RBI regulations, network advisories, and ensure product readiness and compliance. Work with sales and operations teams to enable adoption and resolution of merchant issues. What You’ll Need 4–8 years of product management experience, with at least 2 years in card payments, acquiring, or processing. Strong understanding of card acquiring infrastructure, transaction lifecycle, settlement, MDR, and risk/fraud handling. Experience in working with card networks (Visa, Mastercard, Rupay), acquiring banks, or payment processors. Data-driven decision-making with hands-on experience in SQL, Excel, or dashboarding tools. Excellent stakeholder management, cross-functional collaboration, and problem-solving skills. Familiarity with RBI and PCI-DSS compliance standards is a plus. Why Join Us Be a key player in shaping the card payments experience for millions of Indian merchants. Solve for scale: Handle transaction volumes at one of the largest payment processors in India. Work with some of the most talented teams across product, engineering, and design. Join a fast-paced, impact-driven environment with a focus on innovation, ownership, and excellence. Compensation : If you are the right fit, we believe in creating wealth for you With enviable 500 mn+ registered users, 17 mn+ merchants and depth of data in our ecosystem, we are in a unique position to democratize credit for deserving consumers & merchants – and we are committed to it. India’s largest digital lending story is brewing here. It’s your opportunity to be a part of the story!

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) documentation for quality characteristics, including manufacturability, serviceability, testability, reliability, and product requirements. Hands on experience with tools package release process for both Software & Hardware tools/accessories Review non product/off-the shelf tools for products Experience in software or hardware design transfer process for tools or products Familiar with ISO 13485, IEC 62304, ISO 14971, IEC 60601, 21 CFR part 820, 21 CFR part 11, EUMDR and product specific industry standards. Ensure that product development projects and changes to existing products are conducted in compliance with IEC 62304, FDA Quality System Regulations, EU MDR and inhouse Standards. Participate on cross-functional teams to develop product risk management file (risk management plan, risk assessments, DFMEA, and risk management report). Assist in the creation of verification and validation plans, protocol and reports. Oversee testing and analysis for standards and product requirements compliance. Hanson experience in SW anomaly evaluation and disposition, complaint investigation, NC/CAPA Ensure successful transfer of new products/tools to production facility by assisting in development of process validation requirements (PFMEA, IQ, OQ, PQ) using appropriate statistical tools and techniques. Review Design History Files and Technical Files for conformance to applicable requirements. Participate when appropriate in audits Ensures applicability to SOUP / OTS validations in the product development Participate and provide input to training on department / procedures and policies Hands-on experience on Software Risk Management, Design Controls. Develop templates and training based on the quality system regulations, applicable standards and guidance. Independently reviews all SW deliverables to ensure compliance with development process and the standard. Deliver presentations to the QA organization on status and issues of assigned projects. Deliver training to departments outside of QA. Previous experience working in a cross-functional team environment. Provide Quality support to facilitate resolution of product complaints and/or safety issues Provide support to the Regulatory Department in writing technical submissions. Required Knowledge And Experience B E or B.Tech Minimum 6-8 years of quality engineering experience or equivalence and overall 8-12 years of experience Previous experience working in a cross-functional team environment. Familiar with statistical software tools (Minitab, Stat Graphics) Working knowledge of and auditing experience to the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive. Strong in software design and development, software verification and validation activities Computer literate and experience with PCs, networks, applications, software development life cycle Travel may be required Knowledge in cybersecurity Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people. We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission, and our commitment to diversity here

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 solutions. You will be the voice of the merchant and the architect of high-SR, low-latency, and regulation-compliant card payment infrastructure. Ke y Responsibilities:- Own the end-to-end lifecycle of card acquiring products – from strategy and roadmap to execution and post-launch performance. Define product features and enhancements focused on card payment acceptance across POS, online, and in-app channels. Integrate and manage partnerships with issuer and acquirer banks, card networks, and processors. Monitor and drive improvements in key metrics such as transaction success rate (SR), latency, authorization rates, fraud, and chargebacks. Lead initiatives related to card tokenization, contactless/NFC enablement, recurring payments (SI on cards), and international acceptance. Collaborate with engineering, design, risk, legal, and compliance to ensure scalable and compliant rollout of features. Track RBI regulations, network advisories, and ensure product readiness and compliance. Work with sales and operations teams to enable adoption and resolution of merchant issues. What You’ll Need 4–8 years of product management experience, with at least 2 years in card payments, acquiring, or processing. Strong understanding of card acquiring infrastructure, transaction lifecycle, settlement, MDR, and risk/fraud handling. Experience in working with card networks (Visa, Mastercard, Rupay), acquiring banks, or payment processors. Data-driven decision-making with hands-on experience in SQL, Excel, or dashboarding tools. Excellent stakeholder management, cross-functional collaboration, and problem-solving skills. Familiarity with RBI and PCI-DSS compliance standards is a plus. Why Join Us Be a key player in shaping the card payments experience for millions of Indian merchants. Solve for scale: Handle transaction volumes at one of the largest payment processors in India. Work with some of the most talented teams across product, engineering, and design. Join a fast-paced, impact-driven environment with a focus on innovation, ownership, and excellence. Compensation : If you are the right fit, we believe in creating wealth for you With enviable 500 mn+ registered users, 17 mn+ merchants and depth of data in our ecosystem, we are in a unique position to democratize credit for deserving consumers & merchants – and we are committed to it. India’s largest digital lending story is brewing here. It’s your opportunity to be a part of the story!

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 maturing of 'playbooks' for operational response to cyber threats Operate autonomously to further investigate and escalate in accordance with policies, procedures and defined processes Mentoring and guiding the SOC analysts Lead SOC analysts during incident response actions, advise and coordinate with leadership during active incidents Identify and develop SOC related metrics via dashboard and/or reports for client engagements What we look for, 4+ years experience in SOC or similar capacity (Having experience in MSSP environments will be advantageous) A degree in Computer Science, IT or a Cyber-Security related field. One or more cybersecurity related certification (CySA+, CEH, CSA, ECIH, Cloud & etc). Ability to work and collaborate in a team and lead projects and engagements effectively utilizing resources. Experience in handling SOC daily operations and process / procedure management Strong skills in incident response and technical documentation Experience leading high performing technical teams Strong communication skills is essential Strong leadership qualities and the ability to motivate Experience in engaging in cloud security incidents and SIEM Engineering will be an added advantage. Continuously developing investigative and cybersecurity skills through research and training.