606 Mdr Jobs - Page 5

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and international regulatory standards, preparing regulatory submissions, and maintaining close collaboration with internal teams and channel partners. Key Responsibilities Ensure compliance of all medical devices with national and international regulatory requirements and standards. Prepare, compile, and submit regulatory submissions such as 510(k), PMA, and market registrations for global markets. Liaise with regulatory authorities (e.g., FDA, CDSCO) to address queries and facilitate product approvals. Monitor, interpret, and communicate changes in medical device regulations and assess their impact on the organization. Provide regulatory guidance, support, and training to cross-functional teams (R&D, QA/RA, Product Development, etc.). Develop and implement regulatory strategies to enable new product development and market expansion. Maintain accurate, organized, and up-to-date documentation for regulatory compliance and audits. Collaborate effectively with channel partners and documentation specialists to ensure regulatory alignment across functions. Requirements Bachelor’s degree in Biomedical Engineering, Electronics & Communication, or a related discipline. 3–4 years’ experience in regulatory affairs for medical devices. Comprehensive knowledge of domestic and international medical device regulations (e.g., FDA, EU MDR, ISO 13485, CDSCO). Excellent verbal and written communication skills. Strong attention to detail with analytical thinking and problem-solving abilities. Ability to work effectively in a collaborative, cross-functional team environment. Preferred Qualifications Regulatory Affairs Certification (RAC). Experience working with Class II or III medical devices. Familiarity with quality systems such as ISO 13485 and FDA QSR. Benefits And Perks Competitive salary and performance-based incentives Opportunities for professional development and regulatory training Supportive work environment with experienced industry professionals Exposure to international regulatory processes Health and wellness benefits Skills: regulatory compliance,regulatory affairs,communication,liaison with regulatory authorities,documentation management,compliance,collaboration,medical devices,regulations,regulatory guidance,regulatory submissions,analytical thinking,channel partners,problem-solving

Job Title Medical Device Regulatory Affairs Specialist Location: Bhopal, Madhya Pradesh Company Intense Medical & Dental System Pvt Ltd About The Company Intense Medical & Dental System Pvt Ltd is a leading provider of innovative medical and dental solutions, committed to delivering safe, effective, and high-quality products that improve patient care. Our Bhopal-based team relentlessly pursues excellence in technology, compliance, and service. Job Brief We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to oversee and manage regulatory compliance for our medical device portfolio. You will be responsible for ensuring that all products meet applicable national and international regulatory standards, preparing regulatory submissions, and maintaining close collaboration with internal teams and channel partners. Key Responsibilities Ensure compliance of all medical devices with national and international regulatory requirements and standards. Prepare, compile, and submit regulatory submissions such as 510(k), PMA, and market registrations for global markets. Liaise with regulatory authorities (e.g., FDA, CDSCO) to address queries and facilitate product approvals. Monitor, interpret, and communicate changes in medical device regulations and assess their impact on the organization. Provide regulatory guidance, support, and training to cross-functional teams (R&D, QA/RA, Product Development, etc.). Develop and implement regulatory strategies to enable new product development and market expansion. Maintain accurate, organized, and up-to-date documentation for regulatory compliance and audits. Collaborate effectively with channel partners and documentation specialists to ensure regulatory alignment across functions. Requirements Bachelor’s degree in Biomedical Engineering, Electronics & Communication, or a related discipline. 3–4 years’ experience in regulatory affairs for medical devices. Comprehensive knowledge of domestic and international medical device regulations (e.g., FDA, EU MDR, ISO 13485, CDSCO). Excellent verbal and written communication skills. Strong attention to detail with analytical thinking and problem-solving abilities. Ability to work effectively in a collaborative, cross-functional team environment. Preferred Qualifications Regulatory Affairs Certification (RAC). Experience working with Class II or III medical devices. Familiarity with quality systems such as ISO 13485 and FDA QSR. Benefits And Perks Competitive salary and performance-based incentives Opportunities for professional development and regulatory training Supportive work environment with experienced industry professionals Exposure to international regulatory processes Health and wellness benefits Skills: regulatory compliance,regulatory affairs,communication,liaison with regulatory authorities,documentation management,compliance,collaboration,medical devices,regulations,regulatory guidance,regulatory submissions,analytical thinking,channel partners,problem-solving

Come join Deepwatch’s team of world-class cybersecurity professionals and the brightest minds in the industry. If you're ready to challenge yourself with work that matters, then this is the place for you. We're redefining cybersecurity as one of the fastest growing companies in the U.S. – and we have a blast doing it! Who We Are Deepwatch is the leader in managed security services, protecting organizations from ever-increasing cyber threats 24/7/365. Powered by Deepwatch’s cloud-based security operations platform, Deepwatch provides the industry’s fastest, most comprehensive detection and automated response to cyber threats together with tailored guidance from dedicated experts to mitigate risk and measurably improve security posture. Hundreds of organizations, from Fortune 100 to mid-sized enterprises, trust Deepwatch to protect their business. Our core values drive everything we do at Deepwatch, including our approach to tackling tough cyber challenges. We seek out tenacious individuals who are passionate about solving complex problems and protecting our customers. At Deepwatch, every decision, process, and hire is made with a focus on improving our cybersecurity solutions and delivering an exceptional experience for our customers. By embracing our values, we create a culture of excellence that is dedicated to empowering our team members to explore their potential, expand their skill sets, and achieve their career aspirations, which is supported by our unique annual professional development benefit. Deepwatch Recognition Includes 2025, 2024, 2023, 2022 and 2021 Great Place to Work® Certified 2024 Military Times Best for Vets Employers 2024 US Department of Labor Hire Vets Gold Award 2024 Forbes' America's Best Startup Employers 2024 Cyber Defense Magazine, Global Infosec Awards 2023 and 2022 Fortress Cybersecurity Award 2023 $180M Series C investment from Springcoast Capital Partners, Splunk Ventures, and Vista Credit Partners of Vista Equity Partners 2022 Cybersecurity Excellence Award for MDR Position Summary We are seeking a highly motivated product manager to drive the adoption and growth of our products and services. The successful candidate will have a strong understanding of and experience in product management, with a track record of driving product execution, adoption, and growth. They will work closely with cross-functional teams to understand customer needs and market trends, and develop and implement strategies to bring new product features and services to market. You will have the opportunity to lead the growth of core products that are critical to the success of our organization and our customers. You will work with cross-functional teams to identify customer needs, understand technology landscape and innovate, all while gaining valuable experience in the cybersecurity industry. You will also have the chance to make a real impact on the direction and success of the company and play a key role in driving adoption and growth. In This Role You’ll Get To Increase adoption and usage of our products within the organization and among customers. Improve customer satisfaction, as measured by customer feedback and retention rates. Enhance design and capabilities, based on customer feedback and market trends. Increase revenue and profitability, through pricing and packaging strategies, marketing and sales efforts, and partnerships. Strengthen our market position through competitive analysis and differentiation strategies. Improve cross-functional teamwork and collaboration, through effective communication and leadership. Make strong data driven decisions that align to a broader vision of the company mission and vision To be successful in this role you’ll need to: Execute disciplined product management: Leverage frameworks and methods to ensure viability, feasibility and desirability. Identify customer needs and market trends: Conduct market research and gather customer feedback to understand the needs and preferences of our customers. Develop product strategies: Use your understanding of customer needs and market trends to define product vision, goals, and roadmaps. Collaborate with cross-functional teams: Work closely with teams such as engineering, sales, marketing, and customer success to bring products to market and drive their adoption and growth. Define pricing and packaging strategies: Determine pricing and packaging options for products based on customer needs and market trends. Enablement: Partner with sales, marketing, channel partners, engineering, and delivery teams to ensure they are set up for success. Work with partners and third-party vendors: Identify and cultivate relationships with partners and third-party vendors to support the development and growth of our products. In The First 90-days, You’ll Need To 30-Days Get to know your team & tools: Get to know the team and product landscape. Understand the tools we use and how we use them. Get to know your stakeholders: Spend time getting to know stakeholders on our executive team, marketing, sales, and delivery. Get to know the delivery team: Meet and build relationships with the delivery teams. Understand their perspectives and empathize with their day in day out work. Get to know your customers: Participate in customer conversations and understand the customer landscape. Work with our internal teams to grasp customer themes and opportunities. 60-Days Identify opportunity areas: Work to draft out key initiatives associated with improving the product offerings while leveraging input from stakeholder teams. Draft product vision and roadmap: Start to document your findings and cast the future of product improvements. 90-Days Streamline customer feedback pipeline: Instill a process and tooling to get as much customer feedback as soon as possible to be leveraged in making decisions. Start executing: Drive the product! Life At Deepwatch For employees, Deepwatch fosters a unique, flexible work environment designed with collaboration in mind. The company emphasizes personal and professional growth, offering benefits such as professional development programs, comprehensive health coverage, and generous parental leave. Deepwatch is also committed to diversity, equity, inclusion, and belonging, aiming to empower underrepresented groups in tech by connecting them with meaningful opportunities, mentors, and sponsors. In recognition of its supportive workplace culture, Deepwatch earned the Great Place To Work Certification/(TM) in 2025, underscoring its dedication to creating a positive and inclusive work environment. Deepwatch is a global cybersecurity company with offices in San Francisco Bay Area, CA; Tampa, Florida; and Bengaluru, India. What We Offer At Deepwatch, we are committed to supporting our employees with a comprehensive benefits package designed to enhance your well-being and financial security. We Partner With Plum Benefits To Provide ✔ Group Health Insurance – Comprehensive medical coverage for you and your dependents. ✔ Group Accidental Insurance – Financial protection in case of accidental injuries. ✔ Group Term Life Insurance – Security for your loved ones in unforeseen circumstances. For additional details, refer to the benefits guide provided by Plum. Payroll & Compensation ✔ Pay Cycle: Salaries are processed monthly and paid on the last day of each month. ✔ Pay Slips & Reimbursements: Delivered via email. ✔ Payroll Processing: Managed by BCL Chartered Accountants through GreytHR, which provides tax and payment-related details.

Product Management Consultant Product Development Management is a fast-paced environment where innovative thinking is prized. Our team focuses on the delivery of products or computer-based systems for external customers. We lead and deliver the entire lifecycle from product definition and planning through to production and release. We also oversee modifications, upgrades and maintenance of the product or product line. And to make the whole process run smoothly and seamlessly, we’re experts in project management, from initiation through to delivery, and liaise with other departments on technical matters. Join us to do the best work of your career and make a profound social impact as a Product Management Consultant on our Product Management Team in Pune. What You’ll Achieve As a Product Management Consultant, you will be responsible for shaping Dell’s Data Protection security strategy and driving the development of innovative, secure solutions across our portfolio. You will work with cross-functional teams and some of the world’s most security-conscious customers to deliver technologies that protect mission-critical data and ensure compliance in a rapidly evolving cybersecurity and regulatory landscape. You will: Drive innovation and strategic prioritization by identifying differentiated security features through market and competitive analysis, aligning initiatives with business goals, and championing capabilities that advance our data protection offerings. Lead cross-functional product execution by partnering with engineering, sales, channel partners, and customers to define security requirements and deliver impactful, customer-centric solutions. Leverage deep technical acumen to engage in architectural and functional design discussions, evaluate trade-offs, challenge assumptions, and assess security risks associated with key decisions. Act as the Data Protection Security subject matter expert, supporting field teams and customers with clear guidance, documentation, and advocacy around product capabilities, strengths, and limitations. Coordinate urgent security incident responses with urgency and precision by collaborating with Engineering, Legal, Support, Communications, and incident response teams to ensure effective resolution of high-impact vulnerabilities. Take the first step towards your dream career Every Dell Technologies team member brings something unique to the table. Here’s what we are looking for with this role: Essential Requirements 5+ years of Product Management experience, or equivalent experience in engineering, support, or technical sales within the enterprise data protection and/or security domain. End-to-end technical expertise in security and data protection, including encryption (in-flight and at-rest, key management), identity and access management (LDAP/AD, SSO, SAML, OIDC, OAuth 2.0, MFA, RBAC/ABAC), PKI, CA certificates; and security best practices for OS, containerized, and cloud environments (Linux, Kubernetes, AWS, Azure, etc.). Proven ability to create and maintain a prioritized product roadmap, communicate it effectively to stakeholders, and adapt based on market feedback and business needs. Expertise in evaluating and prioritizing competing product opportunities and features using established frameworks, with strong decision-making skills that balance business value, technical feasibility, and resource constraints. Strong analytical and communication skills, with the ability to translate customer needs, product usage data, and market trends into actionable insights, while aligning cross-functional teams and building productive stakeholder relationships. Desirable Requirements Familiarity with modern security ecosystems (SIEM, SOAR, XDR, MDR), third-party security integrations, and regulatory frameworks (CRA, DORA, NIS2, SOC 2, APL, FIPS). Understanding of the impact of AI on security and data workflows, including anomaly detection, predictive threat intelligence, and AI/ML platform integration. Experience with go-to-market strategy execution including product positioning, pricing, messaging, launch planning, and sales enablement; proven bias for action and ownership mentality in driving cross-functional initiatives and product success. Who We Are We believe that each of us has the power to make an impact. That’s why we put our team members at the center of everything we do. If you’re looking for an opportunity to grow your career with some of the best minds and most advanced tech in the industry, we’re looking for you. Dell Technologies is a unique family of businesses that helps individuals and organizations transform how they work, live and play. Join us to build a future that works for everyone because Progress Takes All of Us. Application closing date: 30 Sep 2025 Dell Technologies is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. Read the full Equal Employment Opportunity Policy here. Job ID: R267618

Company Description MX MDR TECHNOLOGIES LIMITED is a leading manufacturer of high-quality electronic accessories, cables, and spare parts in India, established by Mr. Mukesh Panjwani. MX has a vast network of over 115 distributors across India and exports to various countries including Nepal, Bhutan, and the Middle East. The company offers over 5000 high-quality electronic products known for their excellent quality, reliable service, timely delivery, and reasonable prices. MX products are widely used in homes, commercial offices, industries, and public security sectors. Focusing on quality, service, reliability, adaptability, and innovation, MX is a heritage of trust and credibility, committed to connecting the future. Role Description This is a full-time, on-site role for an Electronic Technician located in Vasai. The Electronic Technician will be responsible for assembling and testing electronic units, performing maintenance and repair tasks, troubleshooting electrical issues, and soldering components. The role involves ensuring all electronic systems and products meet the company's quality standards and safety regulations. The technician will work closely with the engineering team to implement improvements and upgrades as needed. Qualifications Proficiency in Electronics Technology, including understanding and working with various electronic components Skilled in Soldering and Troubleshooting electronic circuits and systems Experience with Electricity, including safe handling practices and electrical systems Knowledge in Maintenance & Repair of electronic devices and systems Strong problem-solving and analytical skills Attention to detail and commitment to quality Ability to work collaboratively with a team Prior experience in a similar role is advantageous

Come and join a 10-year-old, Fastest Growing, IT Managed Services. We have open positions at various levels throughout the organization. About TeamLogic IT Assist Were a 100-person, $22M managed services provider operating across PA, NJ, NC and FL. Our culture is built on Empathy, Transparency, and Data-Driven Decision-Making, and our mission is simple: Make fans of clients, coworkers, and vendors. For three years running weve been named a Best Place to Work in PA, and we maintain a 98% CSAT and 89 NPS. Our Motto is simple yet powerful: MAKE FANS OUT OF OUR CLIENTS MAKE FANS OUT OF OUR VENDORS MAKE FANS OUT OF EACH OTHER We pride ourselves in creating a family-oriented culture and creating a career path for every employee. We invest all our energy in making sure that you achieve your career goals. We are proud of our Glassdoor Review of 5.0 of employee testimonials. Check it out yourself. https://www.glassdoor.com/Reviews/TeamLogic-IT-Newtown-Reviews- EI_IE222125.0,12_IL.13,20_IC1152654.htm Company Website: https://www.teamlogicit.com/ Position Name - NOC & Security Specialist I Department : Security Operations Reports To : Director of Technology Employment Type : [Full-time] Job Location - India (Remote) Overview: The Network Operations & Security Specialist I serves as a first line of defense for security events while also supporting key NOC functions such as daily monitoring, incident response, network performance assurance, and system uptime. This hybrid role is critical to early threat detection, initial incident response, and proactive infrastructure monitoring to prevent critical outages or breaches. The ideal candidate will be hands-on with tools and platforms in both the cybersecurity and network operations domains and play a key role in maintaining service reliability and security for our clients. Key Responsibilities: Security Operations: Monitor alerts and events from SIEMs, EDR/MDR platforms, and other security tools. Perform initial triage and classification of security incidents. Investigate low-severity alerts and perform response and remediation activities where applicable. Escalate high-risk or complex security incidents to senior Security Advisors and Management. Collaborate with partner MDR and SOC vendors to collect additional context or execute recommended actions. Assist in onboarding, tuning, and maintaining security platforms (e.g., EDR, MDR, SIEM). Maintain detailed documentation for security incidents and actions taken. Support the development and enforcement of internal SecOps policies and procedures. Stay current on emerging threats, vulnerabilities, and mitigation strategies. Network Operations Center (NOC): Monitor the health and performance of client environments using RMM and NOC monitoring tools. Proactively identify and respond to service degradations, outages, and other network/system issues. Perform basic troubleshooting of hardware, network, and system-related problems. Communicate status updates for incidents to internal teams, clients, and management. Ensure tickets are properly documented, prioritized, and resolved within defined SLAs. Prepare standard daily, weekly, and monthly operations and availability reports. Coordinate with team members to ensure smooth handoffs and coverage across shifts. Position Requirements: Education : An associate degree in computer science, information technology, cybersecurity, or a related field. OR- 2 or more years of professional experience in an equivalent position. Technical Skills : Foundational knowledge of cybersecurity principles, threats, and vulnerabilities. Familiarity with: Firewalls, antivirus software, EDR/MDR platforms. SOC/SIEM tools and IDS/IPS systems. Network infrastructure, IP networking, and common protocols (TCP/IP, DNS, DHCP, etc.). Experience working with: PSA and RMM tools (e.g., Autotask, NinjaOne, ConnectWise, etc.) BCDR tools and SaaS environments. Microsoft Windows (desktop and server) and virtualized environments. Additional Skills : Excellent customer service and communication skills, with a strong focus on customer satisfaction. Ability to work independently and manage a flexible schedule. Strong documentation skills to record activities and solutions thoroughly and accurately. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Ability to work in a fast-paced and dynamic environment. Willingness to work rotational shifts, including nights and weekends. Preferred Qualifications : Relevant certifications such as CompTIA Security+ or equivalent. Work experience for a Managed Services Provider services multiple client environments Physical Requirements : None Work Environment : This is a fully remote role Application Process : Interested candidates should submit their resume and a cover letter detailing relevant experience and qualifications. TeamLogic IT is committed to creating a diverse environment and is proud to be an equal opportunity employer. We do not discriminate based on race, color, religion, national origin, age, sex, disability, genetic information, veteran status, sexual orientation, gender identity, or any other status protected under applicable federal, state, or local laws. We encourage all qualified candidates to apply and join our inclusive and welcoming team.

At Armor, we are committed to making a meaningful difference in securing cyberspace. Our vision is to be the trusted protector and de facto standard that cloud-centric customers entrust with their risk. We strive to continuously evolve to be the best partner of choice, breaking norms and tirelessly innovating to stay ahead of evolving cyber threats and reshaping how we deliver customer outcomes. We are passionate about making a positive impact in the world, and we’re looking for a highly skilled and experienced talent to join our dynamic team. Armor has unique offerings to the market so customers can a) understand their risk b) leverage Armor to co-manage their risk or c) completely outsource their risk to Armor. Learn more at: https://www.armor.com Summary We are seeking a dedicated Technical Support Engineer L1 to join our cybersecurity Support team. As the first point of contact for our global customers using our Managed Detection and Response (MDR) solutions, you will play a crucial role in ensuring customer satisfaction while maintaining the security and functionality of their systems. Essential Duties and Responsibilities (Additional duties may be assigned as required) Provide technical support to global customers for our MDR platform and related cybersecurity products Monitor systems and network health, generating usage reports and tracking potential security issues Diagnose and troubleshoot basic software problems related to our MDR solutions Manage customer incidents using our ticketing system, ensuring timely resolution according to service level agreements Document incidents, solutions, and maintain accurate records for future reference Assist with basic configuration and deployment of MDR sensors, agents, and monitoring tools Identifying potential problems from Microsoft Sentinel / MS Azure / MS Defender logs Participate in 24x7 support rotation to ensure round-the-clock monitoring and incident response Communicate effectively with customers to understand their needs and provide clear technical guidance Required Skills Bachelor's degree in computer science, Information Technology, Cybersecurity or related field (or equivalent experience) 5+ years of experience in technical support, IT Support role, or cybersecurity operations Rudimentary understanding of intrusion detection, firewall operations, and other general security practices. Create VM templates Add/modify/delete disks through VCD Respond to VMWare host and system alerts Intermediate level of networking expertise with understanding of networking fundamentals and well-known protocols/services including GRE, TCP/IP, V-LAN. Proficiency in Windows Server environments and Linux distributions commonly used in enterprise settings Knowledge of managed detection and response (MDR) technologies is a plus Excellent problem-solving skills and keen ability to diagnose and troubleshoot technical issues. Well-spoken and articulate with an attention to detail with excellent writing abilities. Experience with ticketing systems and ITIL methodologies preferred Ability to work in a fast-paced environment and handle multiple priorities simultaneously Willingness to learn new technologies WHY ARMOR Join Armor if you want to be part of a company that is redefining cybersecurity. Here, you will have the opportunity to shape the future, disrupt the status quo, and be a part of a team that celebrates energy, passion, and fresh thinking. We are not looking for someone who simply fills a role – we want talent who will help us write the next chapter of our growth story. Armor Core Values Commitment to Growth: A growth mindset that encourages continuous learning and improvement with adaptability in the face of challenges. Integrity Always: Sustain trust through transparency + honesty in all actions and interactions regardless of circumstances. Empathy In Action: Active understanding, compassion and support to the needs of others through genuine connection. Immediate Impact: Taking initiative with swift, informed actions to deliver positive outcomes. Follow-Through: Dedication to delivering finished results with attention to quality and detail to achieve the desired outcomes. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. The noise level in the work environment is usually low to moderate. The work environment can be either in an office setting or remotely from anywhere. Equal opportunity employer - it is the policy of the company to comply with all employment laws and to afford equal employment opportunity to individuals in all aspects of employment, including in selection for job opportunities, without regard to race, color, religion, sex, national origin, age, disability, genetic information, veteran status, or any other consideration protected by federal, state or local laws.

We are seeking an Cybersecurity – India Sales to lead revenue growth across India. This role is responsible for building deep client relationships, expanding existing accounts, and driving new business across public sector, PSU, energy, infrastructure, and regulated industries. The ideal candidate will bring a sharp understanding of the cybersecurity landscape - particularly OT, SOC, IDAM, managed services, and threat intelligence - and the complex buying ecosystem in India. Preferred Qualifications Bachelor’s degree in Engineering, Computer Science, Business Management or equivalent OR Bachelor's Or Masters Degree in Cybersecurity Cybersecurity certifications (e.g., CISM, CISSP, CEH) and/or OEM-specific sales credentials (AWS, Microsoft, Cisco) Ability to travel 30–40% across metros in India Responsibilities Sales Execution & Target Achievement Achieve quarterly and annual revenue targets across government, PSU, and private enterprise sectors Manage end-to-end sales cycle - from lead identification, pre-sales coordination, bidding, and negotiation to closure Expand footprint within large strategic accounts through farming and cross-sell of solutions Go-to-Market Development Lead RFP-based sales with strong coordination between delivery, pre-sales, and proposal teams Contribute to India-specific sales playbooks, pricing strategies, and GTM campaigns Stakeholder & Ecosystem Management Build and maintain CXO relationships (CIOs, CISOs, CXOs of PSUs, ministries, and large private groups) Partner with Indian OEMs, system integrators, and cybersecurity technology providers for joint wins Represent the company in security expos, government workshops, and industry forums Sales Operations Maintain accurate pipeline tracking and forecasting via CRM tools Collaborate with inside sales, marketing, and delivery teams for account-based selling Share India market insights with leadership to shape future offerings and partnerships Ideal Candidate Profile 12 + years of B2B solution sales experience in cybersecurity, IT services, or critical-infrastructure technologies Demonstrated success in selling to government, PSUs, smart infra, and regulated sectors Experience with SOC, IDAM, managed detection and response (MDR), and OT/ICS/SCADA security Strong RFP/bid management skills, with proven 7/8-figure deal closures Fluent in navigating Indian sales ecosystems, including MeitY, NICSI, BEL, ECIL, NTPC, GAIL, etc. Hands-on experience with CRM systems and structured sales tracking Only B2B solution sales experience in cybersecurity, IT services, or critical-infrastructure can connect with me at 9898791075 OR mail at joy.saha@adani.com

Join a fast-growing Cybersecurity MDR Team ! We're hiring Technical Support Engineers (L1) to support global clients on cutting-edge security solutions. This is not a desktop support role – we need experts in server-side troubleshooting . Key Skills: Linux & Windows Server Administration Virtual Machines, VMWare, VCD Firewall Configurations Network Troubleshooting (TCP/IP, VLAN, GRE) Exposure to Microsoft Sentinel / Azure / Defender logs Knowledge of MDR technologies (advantage) Role Highlights: Troubleshoot and support global clients on cybersecurity & MDR platforms Manage incidents, monitor systems, and provide clear technical guidance Participate in 24x7 support rotations Work with advanced security tools in a high-growth environment 🔹 Mandatory Technical Skills: Linux System Administration (RHEL / CentOS / Ubuntu) Windows Server Administration Virtualization: VMWare (VM creation, management, VCD knowledge) Networking: TCP/IP, VLAN, Firewall configurations, basic troubleshooting Security Tools: Exposure to Microsoft Sentinel / Azure / Defender logs Incident Management: Ticketing tools (ServiceNow / JIRA / similar) What We’re Looking For: Ability to handle technical issues independently Immediate joiners preferred

About the Company Bioscan Research is a MedTech company developing advanced diagnostic and monitoring solutions for brain injuries and trauma care. Our flagship device, CEREBO, is a non-invasive, handheld system leveraging near-infrared spectroscopy and machine learning to detect intracranial injuries such as bleeds and edema. As we expand into regulated markets including the United States and Europe, we are seeking an experienced QA/RA Manager to lead quality and regulatory functions across the organization. Role Summary The QA/RA Manager will be responsible for implementing and maintaining the Quality Management System (QMS) in alignment with international medical device standards, as well as leading regulatory affairs activities required for product approvals and ongoing compliance. This role requires close collaboration with cross-functional teams including R&D, Clinical, Manufacturing, and Leadership. Key Responsibilities Quality Assurance (QA): Lead the implementation, maintenance, and continuous improvement of the QMS in compliance with ISO 13485, 21 CFR 820, and other applicable standards Oversee documentation control, change management, non-conformances, CAPA, internal audits, and employee training programs Ensure design control, risk management, process validation, and device history records are maintained accurately and consistently Coordinate management reviews, supplier qualification, and audit readiness activities Own and maintain key documents such as QSPs, SOPs, and the Device Master Record Regulatory Affairs (RA): Prepare and manage regulatory submissions including US FDA 510(k), CE marking under MDR, CDSCO registration, and other international requirements Monitor and interpret global regulatory changes and integrate them into internal processes and product development lifecycles Maintain the Essential Principles Checklist, GSPR documentation, and support compliance with labeling, UDI, and PMS requirements Coordinate with external consultants, testing laboratories, and notified bodies as needed Support post-market surveillance activities and field safety corrective action procedures Candidate Profile Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, Quality Management, or related field Minimum of 2-5 years of relevant experience in a QA/RA role within a medical device company Strong knowledge of ISO 13485, IEC 62304, ISO 14971, 21 CFR 820, EU MDR, and applicable national regulatory frameworks Demonstrated experience in leading or supporting regulatory submissions and quality audits Strong documentation, communication, and analytical skills Ability to work independently and cross-functionally in a dynamic, high-growth environment Experience with hardware, embedded firmware, or connected health systems is preferred

Mandatory Technical Skills: Linux System Administration (RHEL / CentOS / Ubuntu) Windows Server Administration Virtualization: VMWare (VM creation, management, VCD knowledge) Networking: TCP/IP, VLAN, Firewall configurations, basic troubleshooting Security Tools: Exposure to Microsoft Sentinel / Azure / Defender logs Incident Management: Ticketing tools (ServiceNow / JIRA / similar) Join a fast-growing Cybersecurity MDR Team ! We're hiring Technical Support Engineers (L1) to support global clients on cutting-edge security solutions. This is not a desktop support role – we need experts in server-side troubleshooting . Key Skills: Linux & Windows Server Administration Virtual Machines, VMWare, VCD Firewall Configurations Network Troubleshooting (TCP/IP, VLAN, GRE) Exposure to Microsoft Sentinel / Azure / Defender logs Knowledge of MDR technologies (advantage) Role Highlights: Troubleshoot and support global clients on cybersecurity & MDR platforms Manage incidents, monitor systems, and provide clear technical guidance Participate in 24x7 support rotations Work with advanced security tools in a high-growth environment Job Types: Full-time, Permanent Benefits: Health insurance Internet reimbursement Leave encashment Life insurance Provident Fund Experience: technical support : 5 years (Preferred) linux server: 5 years (Preferred) Microsoft Windows Server: 5 years (Preferred) VMWare: 5 years (Preferred) IP networking: 5 years (Preferred) TCP/IP: 5 years (Preferred) Security tools: 5 years (Preferred) Azure: 4 years (Preferred) defender logs: 5 years (Preferred) Location: Pune, Maharashtra (Preferred) Work Location: In person

Job Title: Labelling Specialist - Medical Devices Location: Sanand, Ahmedabad Department: Quality Assurance Employment Type: Full-Time (On-Site) Reports To: Quality Manager Job Summary: We are seeking a detail-oriented and knowledgeable Labelling Specialist to manage the creation, review, and maintenance of labelling content for our medical devices. The ideal candidate will have a strong understanding of medical device regulations and be well-versed in labelling standards, particularly ISO 15223. This role is critical to ensuring our product labels are compliant, accurate, and aligned with global regulatory requirements. Key Responsibilities: Develop and maintain medical device labels artwork in compliance with applicable regulatory requirements. Ensure labelling content aligns with ISO 15223 (Symbols to be used with medical device labels, labelling and information to be supplied). Collaborate with cross-functional teams including Regulatory Affairs, Quality Assurance, R&D, and Marketing to gather and validate labelling information. Review labelling changes and provide regulatory input during product development and product updates. Ensure labels comply with regional regulations such as MDR (EU), FDA (US), and other relevant markets. Maintain labelling documentation and change control records in accordance with internal procedures. Monitor updates to labelling standards and regulations and assess their impact existing labelling. Qualifications and Requirements: Bachelor's degree in a scientific, engineering, or healthcare-related discipline. Minimum 2 years of experience in a regulated medical device environment, preferably in labelling or regulatory affairs. Strong knowledge of ISO 15223 and other applicable standards (e.g., ISO 20417, IEC 60601, UDI regulations). Familiarity with regulatory requirements for labelling under EU MDR, US FDA, and other global regulations. Experience with labelling software tools (CorelDraw, Adobe Illustrator or similar tools) and document control systems is a plus. Excellent written and verbal communication skills. High attention to detail and ability to work independently and in teams.

we specialize in cutting-edge cybersecurity solutions, helping businesses safeguard their digital assets and comply with industry regulations. We’re looking for a dynamic and experienced Cybersecurity Sales Lead to drive our growth strategy and strengthen our client base across industries. Job Description: As a Cybersecurity Sales Lead , you will be responsible for identifying new business opportunities, building strong client relationships, and driving revenue growth for our cybersecurity services. You will work closely with the marketing, technical, and leadership teams to craft client-centric solutions and close high-value deals. Key Responsibilities: Drive B2B sales of cybersecurity products and services (SOC, VAPT, GRC, MDR, etc.) Identify and qualify new leads through networking, outbound outreach, and digital channels Conduct client meetings to understand pain points and propose tailored security solutions Collaborate with technical teams to prepare proposals, POCs, and pricing strategies Own the complete sales cycle – from lead generation to negotiation and closure Achieve monthly and quarterly revenue targets Build and manage a robust sales pipeline using CRM tools Stay up to date on cybersecurity trends, threats, and competitor offerings Represent the company at conferences, trade shows, and webinars when needed Requirements: Bachelor's degree in Business, IT, or a related field (MBA is a plus) 4–7 years of sales experience, with at least 2 years in cybersecurity or IT services Strong understanding of cybersecurity products and services Excellent communication, negotiation, and presentation skills Proven track record of achieving and exceeding sales targets Familiarity with CRM tools (HubSpot, Zoho, Salesforce, etc.) Self-driven, organized, and team-oriented Preferred Skills: Experience selling to mid-size and enterprise clients Knowledge of compliance standards like ISO 27001, SOC 2, GDPR, etc. Existing network of decision-makers in the cybersecurity industry To Apply: Submit your resume along with a short cover letter outlining your relevant experience and why you are the right fit for this role on sandeep.k@cywarden.com Job Types: Full-time, Permanent Pay: ₹600,000.00 - ₹1,000,000.00 per year Work Location: In person

As a Mechanical Engineer with 5 to 7 years of overall experience, including 3 to 5 years in the medical device industry, you will be responsible for utilizing your expertise in CAD software such as Solid Edge & NX, as well as conducting precise engineering calculations. Your proficiency in Geometric Dimensioning and Tolerance stack up analysis will be crucial for the successful execution of your responsibilities. You will be expected to demonstrate your ability to generate alternative mechanisms, concepts, and solutions, with a focus on designing for technical cost reductions. Moreover, you should be capable of performing theoretical calculations for the concepts developed, ensuring accuracy and efficiency in the design process. In this role, you will utilize existing tools and standard methodologies to effectively report and track product, project, and process metrics. Experience in the Design control process and DHF documentation for medical devices will be essential, and familiarity with EU MDD to MDR, Gap Analysis, and Risk Management and Analysis (including FMEA and Failure analysis) will be advantageous. Knowledge of Polarion software is preferred for this position. This is a full-time role with a day shift schedule and a yearly bonus. The work location is in person, and the application deadline is 18/07/2025.,

You should have a minimum of 12 years of experience in Sales, Consulting, or Presales in the cybersecurity domain. A consultative problem-solving services-oriented, solution-led approach and experience are preferred. Your demonstrated ability for consultative sales in the cybersecurity domain should be targeting CISO/CXOs. Skills in areas of risk advisory and various cybersecurity frameworks, along with an understanding of the cybersecurity OEM ecosystem and dexterity in crafting winning services proposals are critical. Expertise in any core security element of Device Management, Network Security, Zero Trust Frameworks, and Managed Detection and Response (MDR) Services is required. Knowledge in Data Security and Privacy, various Industry compliance Frameworks from SEBI, RBI, IRDA, DPDP, Security Assurance, and Cloud Security areas is essential. You should have proven expertise and experience in crafting complex managed security services (MSS) proposals which include multiple cybersecurity domains like network security, device management, security operations, SOC services, etc. Reviewing technology designs with technology architects and engineers while considering local and regional regulatory requirements is part of the role. Experience with assessment of a comprehensive and broad set of security technologies and processes, data protection, identity and access management (IAM), network security within SaaS, IaaS, PaaS, and other cloud environments is necessary. Additionally, expertise in Infra security architecture and any subject matter expertise within network infrastructures and perimeter security technologies such as firewalls, load balancers, WAF, CASB, proxies, SDN, DNS, and DDOS solutions is expected. A solid grasp of private/hybrid/public clouds and legacy IT infrastructures is required. You should be highly familiar with public and private cloud technologies (e.g., AWS, Azure, GCP, VMWare, etc.) and their Security offerings, preferably based on certifications and some hands-on experience. Maintaining in-depth knowledge of the competition's offerings and strategies is important. You will lead the development of integrated solutions, including terms and conditions, to create a final customer proposal. An understanding of emerging technologies & trends like XDR, MDR, CASB, SASE, Microservices, Kubernetes, containers, Intelligent Automation, DevSecOps, Zero Touch, etc., is preferred. A Bachelor's degree or Master's degree is also desirable for this role.,

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 Malware Researcher? Red/Blue/Purple team member? We have a fantastic opportunity here at Sophos Labs for a Threat Researcher role to join our global team of Behavioural Protection engineers, to hunt, to research, and to add real-time protection for suspicious activity across our customer environments. Our team of skilled security experts combine their passion to detect & disrupt cyber-attacks with their capability to develop protection rules that can cut through the noise in modern computing environments to tease out attacker’s nefarious activities. You are intrinsically motivated to understand the core logic behind malware and hacking attacks, to find & predict new ways attackers will modify their techniques and take great satisfaction in developing robust protection logic that is immune to evasive actions. You will be responsible for writing behavioural protection rules that are able to block malicious activities across all types of TTP (even if a Mitre Technique doesn’t exist yet). This is the foundation of Sophos next-gen approach. Above all - you enjoy thinking creatively; combining your deep technical knowledge, your tenacity for innovation, and your can-do attitude to solve complex and challenging problems on daily basis. Additionally, you will also be supporting our remediation effort to remove artifacts left behind, by writing clean-up rules, and supporting our Sandbox development, such as (but not limited to) creating signatures, identifying evasion techniques that prevent the sandbox from running the threat smoothly. What You Will Do Conduct in-depth behavioural analysis of Windows threats Develop Behavioural rules for various threat behaviours including hands-on keyboard attack, malware payloads, initial attack vectors and Advanced Persistent Threats (APTs) Produce quality threat analysis reports for both internal and external audience Assist in sandbox improvements by analysing malware that hinders the sandbox environment in running the threat, which deploys various anti-analysis techniques Develop Clean-up rules to remove artifacts that are left behind by the behavioural protection rules Collaborate with other cross-functional teams to improve behavioural protection capability based on the threat analysis Guide and train junior team members in assisting malware analysis, peer code review Assist in the development of tools wherever necessary to improve day-to-day task What You Will Bring 8+ yrs of strong knowledge of Windows Internals including Memory management, Processes, Threads Proficiency in both static and dynamic analysis of threats, using tools such as IDAPro, WinDbg Demonstrated programming experience. Preferred: Python, Lua Excellent communication skills with the ability to demonstrate complex technical problem to peer researchers as well as to product engineering team Excellent analytical and problem-solving skills with the ability to think strategically and creatively Bachelor’s degree in computer software (Computer Security preferable) or equivalent experience #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

Technical Support Engineer (L1) – Cybersecurity Key Skills: Linux & Windows Server Administration Virtual Machines, VMWare, VCD Firewall Configurations Network Troubleshooting (TCP/IP, VLAN, GRE) Exposure to Microsoft Sentinel / Azure / Defender logs Knowledge of MDR technologies (advantage) Role Highlights: Troubleshoot and support global clients on cybersecurity & MDR platforms Manage incidents, monitor systems, and provide clear technical guidance Participate in 24x7 support rotations Work with advanced security tools in a high-growth environment 🔹 Mandatory Technical Skills: Linux System Administration (RHEL / CentOS / Ubuntu) Windows Server Administration Virtualization: VMWare (VM creation, management, VCD knowledge) Networking: TCP/IP, VLAN, Firewall configurations, basic troubleshooting Security Tools: Exposure to Microsoft Sentinel / Azure / Defender logs Incident Management: Ticketing tools (ServiceNow / JIRA / similar) What We’re Looking For: Ability to handle technical issues independently Immediate joiners preferred

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 The Clinical Evaluation Medical Writer on our Endoscopy team plays a key role in developing and updating clinical evaluation documents (e.g., CEP, CER, PMCFP, PMCFR, SSCP) to support CE Mark submissions and maintain compliance throughout the product lifecycle. This work follows MEDDEV 2.7/1 Rev. 4 and EU Regulation 2017/745 and involves close collaboration with cross-functional teams to gather and interpret data on device safety, performance, and benefit-risk. In addition, the writer supports related activities such as summarizing and disseminating clinical literature and other available data to share relevant evidence, while also managing Medical Information activities. This includes tracking inquiries, monitoring key metrics, researching and responding to technical and clinical questions from both internal teams and external healthcare professionals, all under the appropriate guidance of Clinical and Medical Affairs. Success in this role requires strong skills in scientific writing, literature review, data analysis, and clear communication, along with a proactive and collaborative mindset. Responsibilities may include the following and other duties may be assigned. Independently creates and maintains clinical evaluation documents (CEP, CER, PMCFP, PMCFR, SSCP) in compliance with MEDDEV 2.7/1 Rev 4, MDD, EU MDR 2017/745, MDCG guidance, and company procedures. Supports Medical Information activities by leveraging scientific expertise to research and respond to inquiries from healthcare professionals and internal teams, maintaining related documents and reports. Performs thorough literature searches and reviews clinical evidence from studies, reports, and available post-market data. Summarizes and combines this information to support product submissions, clinical evaluations, and Medical Information inquiries. Reviews scientific materials like abstracts, posters, manuscripts, slides, and promotional content to check for accuracy, proper claims, off-label use, and compliance with company policies. Develops state-of-the-art reports for product families and reviews cross-functional documents such as IFUs and Risk Management files to ensure alignment on safety and risk information. Identifies and reports complaints or adverse events from literature to the Global Complaint Handling team. Creates responses to audit and submission queries and maintains a database of peer-reviewed literature. Collaborates with key stakeholders to drive evidence-based scientific decisions and maintain compliance with regulatory and corporate guidelines. Communicates project timelines, input requirements, and risks clearly and promptly with cross-functional teams. Required Knowledge and Experience: Requires mastery of a specialty area and full knowledge of industry practices, typically obtained through advanced education combined with experience. May have broad knowledge of project management. Requires a Baccalaureate degree and total 8 years of experience with minimum 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience. 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. This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). 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.

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 As a Quality Engineer you will be a key member of the Medtronic Post Market Quality Engineering team responsible for maintaining highest standards of product reliability and patient well-being through gather and analyse data, write reports, and communicate with regulatory agencies on ensuring product safety. Responsible for leading the evaluation of post‑market safety signals arising from medical device complaints. The role entails comprehensive analysis of complaint data to identify trends, assess potential risks, and support regulatory reporting and risk mitigation strategies. 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. Works on post-market documents as requested and needed by the RPM teams. This can include but not limited to signal evaluations and HHE (Health Hazard Evaluations) Assess complaints for completeness and determine need for investigation or signal evaluation Analyse complaint data to identify safety signals or adverse trend patterns for signal detection & evaluation. Conduct statistical evaluation to determine the significance of identified signals Draft signal evaluation reports and adverse event reports (e.g., MDRs) according to FDA, EU MDR, ISO and other global regulatory standards Liaise with engineering, manufacturing, regulatory, clinical, and quality teams to support investigations and CAPA actions Escalate high-risk signals for management review and regulatory notification Ensure investigations and reports comply with 21 CFR 803/820, FDA MDR, ISO 13485, ISO 14971, EU MDR, etc. Support audits, document reviews, and CAPA follow-through as needed Good verbal and written communication skills including plan / report development. Required Knowledge and Experience B E or B.Tech in Mechanical/Biomedical Engineering Minimum 4-6 years of quality engineering experience or equivalence and overall 6-8 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.

Quality Assurance Engineer - Company Overview: Optra Scan Pvt Ltd is a leading provider of digital pathology solutions, revolutionizing the way pathology practices worldwide, managing and interpreting diagnostic information. Our cutting-edge technology empowers pathologists to improve efficiency, accuracy, and patient care through digitalization and artificial intelligence. URL - www.optrascan.com Job Summary: The QA Engineer will support and maintain the Quality Management System (QMS) in compliance with regulatory requirements (e.g., ISO 13485, IEC 62304, FDA 21 CFR Part 820). The role involves ensuring that all products, processes, and documentation meet OptraSCAN’s high standards for quality and regulatory compliance. Key Responsibilities:- · Ensure compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable international quality standards. · Support design control, risk management, validation, and verification processes for scanners and software. · Maintain and improve the Quality Management System (QMS) across departments. · Review and approve SOPs, DHRs, DHFs, CAPAs, NCRs, and change controls. · Conduct internal audits and support external audits (e.g., customer, notified bodies, FDA). · Collaborate with engineering, manufacturing, and regulatory teams to ensure product quality at every stage of the lifecycle. · Support software validation and documentation of AI algorithms per FDA/CE/MDR requirements. · Participate in supplier qualification and vendor audits. · Monitor and report on key quality metrics (e.g., defect rates, complaints, CAPA status). · Ensure traceability and document control throughout product development and release.lease. Qualifications :- · Bachelor’s degree in biomedical engineering, Quality, Life Sciences, or related field. · 3–6 years’ experience in a medical device, diagnostics, or regulated health tech environment. · Familiarity with digital pathology, AI in healthcare, imaging devices, or SaMD is a plus. · Strong knowledge of ISO 13485, ISO 14971, IEC 62304, FDA QSR, and EU MDR/IVDR regulations. · Experience with QMS tools, document control systems, and audit practices. · Excellent written and verbal communication skills. · Detail-oriented,with strong problem-solving and cross-functional collaboration abilities.

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. If this excites you, then apply below. About Indegene - https://www.indegene.com/ Summary: Experienced Senior Design Quality Engineer with a strong focus on ensuring product quality across the entire lifecycle—from concept through post-market—by leading Quality Plan development, validating critical design inputs, and ensuring compliance during design reviews, verification, validation, and transfer. Skilled in risk management, design for reliability (FMEA, V&V, RCA), and post-market analysis to drive continuous improvement. Proven ability to collaborate cross-functionally to deliver high-quality, customer-focused, and regulatory-compliant products. Roles and responsibilities: Ensures that appropriate quality plans are made that include all stages of the life cycle of the product and support Quality Plan design. Provides effective oversight of the execution of the Quality Plan, any Risk Management activities, and all design-related activities during the product/system lifecycle. Validates key design inputs like usability, reliability, Performance, supportability, manufacturability, localizability, security, Privacy, serviceability, sustainability, and costs. Performs assessment of product quality performance and post-market product quality analysis. Uses post-market analytics and statistics to report on product quality performance in the field (provide feedback to manufacturing, suppliers, or design teams) and initiates field actions when enquired. Ensure compliance requirements are met during design reviews, design Verification, validation, and design transfer. Apply and Facilitate design for quality and reliability best practices (FMEA, robust design, V&V, RCA, Problem-solving). Skills: Applied knowledge of appropriate global medical device or consumer product regulations, requirements, and standards (21 CFR Parts 820, ISO13485, ISO14971, MEDDEV, EU MDR, etc.). Experience or understanding of Software or Hardware development, Verification and Validation, Risk management, RCA, Requirements Management, Design, and Usability. Understand Sample Size Determination and Statistical Methods, Safety Risk Management (i.e ISO 14971), and Failure Modes and Effects Analysis (FMEA) / Fault Tree Analysis. Understand a quality system and its development, documentation, and implementation with respect to domestic and international standards or requirements. Understand the audit process including types of audits, planning, preparation, execution, reporting results, and follow-up. Be able to develop and implement quality programs, including tracking, analyzing, reporting, and problem solving. Soft Skills: Leadership, cross-functional collaboration, problem-solving, strong verbal & written communication, project management, decision-making, attention to detail Qualifications: Bachelor's degree(B.E. / B.Tech) Minimum 3 years of experience in medical device related Quality & Regulatory domain & working knowledge on design control principles EQUAL OPPORTUNITY Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

Role: Full time Employment. Position: MDR SOC Manager Experience: 8+ Years Interview Mode: F2F Work from Office - 1st Floor, West Wing, Khanija Bhavan, #49, Race Course Road, Bangalore 560001. Rotational Shifts. Qualification: BE/B.Tech OR MCA Roles and Responsibilities: 1. Team Leadership and Operational Oversight: Lead and manage SOC Analysts, providing real-time guidance, performance coaching, and task prioritization. Ensure the team delivers timely, accurate, and complete triage, investigation, andescalation of security alerts across customer environments. Maintain shift alignment, performance expectations, and documentation standards for24/7 SOC operations. 2. Escalation and Incident Response Coordination: Act as a senior escalation point for high-priority alerts and operational anomalies encountered by frontline analysts. Ensure appropriate handoff and escalation of significant incidents to senior analyst teams with full context and documentation. Participate in incident response processes as needed to support the triage of critical security events. 3. Customer Service and Engagement. Oversee analyst interactions with customers, ensuring prompt and professional communication around alerts and triage outcomes. Support client escalations and service-impacting concerns, resolving issues with urgency and precision. Foster a customer-first culture across the team, ensuring that all security concerns are addressed with diligence and clarity. 4. Training and Mentorship: Provide regular feedback, mentorship, and technical coaching to SOC Analysts to elevate investigative quality and confidence. Support onboarding of new team members and lead peer-based training initiatives to Insure consistent standards. Promote a knowledge-sharing environment that encourages continuous learning and professional growth. 5. Process Management and Workflow Optimization: Monitor and refine alert handling procedures, ensuring compliance with SOC playbooks, detection logic, and service-level expectations. Identify and resolve workflow bottlenecks while recommending improvements to tooling, documentation, and triage methodologies. Collaborate with internal teams to implement enhancements to threat detection, signal tuning, and case management efficiency. 6. Cross-Team Collaboration: Coordinate effectively with other MDR teams to ensure seamless escalation, incident response, and detection alignment. Contribute to working groups focused on detection tuning, SOC maturity, and threat- hunting enhancement. Share frontline insights with engineering and threat intelligence teams to support data- driven improvement. 7. Shift and Resource Management: Manage shift schedules, maintain coverage plans for holidays and surge periods, and Educational Qualifications: Bachelors degree in Cybersecurity, Information Technology, or a related field. A combination of education and professional experience will be considered. Certifications: Industry certifications such as CISSP, CISM, CEH, GIAC, or equivalent are strongly preferred.

Career Area: Engineering : Your Work Shapes the World at Caterpillar Inc. When you join Caterpillar, you'rejoining a global team who cares not just about the work we do but also about each other. We are the makers, problem solvers, and future world builders who are creating stronger, more sustainable communities. We don'tjust talk about progress and innovation here we make it happen, with our customers, where we work and live. Together, we are building a better world, so we can all enjoy living in it. Job Summary Caterpillar is seeking a highly motivated and experienced Senior Design Engineer to join our team focused on genset applications. This role is critical in delivering high-performance, compliant, and manufacturable solutions. The ideal candidate will bring strong technical expertise in mechanical design and a collaborative mindset to work effectively with global teams Role Definition Designs, develops, builds, and implements new products, components, or technologies. Responsibilities Lead design and development of fuel tanks ensuring compliance with Caterpillars engineering standards and regional regulations. Perform structural integrity for seismic conditions, load distribution, lifting and transportation loads. Develop and validate sheet metal designs, ensuring manufacturability with knowledge of welding standards (heat load/warpage) and cost-effectiveness. Collaborate directly with global teams across the regions to align design requirements and project goals. Knowledge on Creo, PLMs and supplier engagement is added advantage. Required Qualifications Bachelors/Master's degree in Mechanical Engineering or a related field. Proven experience in fuel tank design, preferably for gensets or similar mechanical systems. Skill Descriptors Analytical Thinking Knowledge of techniques and tools that promote effective analysis; ability to determine the root cause of organizational problems and create alternative solutions that resolve these problems. Level Extensive Experience: Seeks discrepancies and inconsistencies in available information; explains variances. Organizes and prioritizes the sequence of steps to be taken to remedy the situation. Identifies many possible causes for a problem based on prior experience and current research. Quantifies the costs, benefits, risks and chances for success before recommending a course of action. Approaches a complex problem by breaking it down into its component parts. Chooses among a diverse set of analytical tools according to the nature of the situation. Effective Communications Understanding of effective communication concepts, tools and techniques; ability to effectively transmit, receive, and accurately interpret ideas, information, and needs through the application of appropriate communication behaviors. Level Extensive Experience: Reviews others' writing or presentations and provides feedback and coaching. Adapts documents and presentations for the intended audience. Demonstrates both empathy and assertiveness when communicating a need or defending a position. Communicates well downward, upward, and outward. Employs appropriate methods of persuasion when soliciting agreement. Maintains focus on the topic at hand. Managing Multiple Priorities Knowledge of effective self-management practices; ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation. Level Extensive Experience: Clarifies and handles multiple concurrent and diverse activities. Shifts focus among several efforts as required by changing priorities. Addresses potential conflicts that impact current delivery commitments. Works with or leads others to re-prioritize work and reschedule commitments as necessary. Responds to shifting priorities while maintaining progress of regularly scheduled work. Demonstrates an expectation that there will be ongoing shifts in demands and priorities. Technical Excellence Knowledge of a given technology and various application methods; ability to develop and provide solutions to significant technical challenges. Level Extensive Experience: Advises others on the assessment and provision of all technical solutions. Engages appropriate subject matter resources to effectively resolve technical issues. Mentors others to enhance their technical competence and its application to achieve more effective technical solutions. Coaches others in promoting, defining, analyzing, and providing superior technical solutions to business problems. Provides effective solutions to moderate technical challenges through strong technical competence, effectively examining implications of events and issues. Assumes accountability for personal technical performance and holds others responsible for theirs. Computer-Aided Design & Engineering Knowledge of tools and techniques of specialized graphics programs; ability to produce, analyze, simulate and test product design drafts. Level Extensive Experience: Coaches others on orthographic, isometric and axonometric projections. Presents complex products and systems graphically. Performs manipulations on design objects, such as changing projections and managing drawing layers. Directs the matrix computations performed to transform objects in coordinate space. Consults on benefits and drawbacks of top-down design vs. bottom-up design. Compares and contrasts uses of bird's-eye views and worm's-eye views. Product Design - MFG Knowledge of processes, approaches, tools and techniques of product design; ability to convert customer and market requirements into product design. Level Extensive Experience: Develops improvement plans for senior management and evaluates the outcome of the design against the functionality. Advises others on the development of multiple products and their functionality. Trains others on advanced tools and approaches of product design. Monitors the processes and procedures of a complex product design to ensure functional requirements are met. Evaluates feedback from customers and consults on functional weaknesses. Controls design and development costs of a proposed product through effective resource coordination. Product Design and Developmen tKnowledge of product features; ability to design, build, and develop a new product, technology, or service from concept through to production. Level Extensive Experience: Develops organizational standards and processes in order to maximize complex product services' efficiency and effectiveness. Creates and introduces new techniques that expedite or simplify the development process. Supervises the management of multiple and diverse types of products or services. Develops proof-of-concept exercises to prove or disprove validity of proposed products. Advises on the appropriate solutions to complex product design and development problems. Designs working prototypes of a variety of proposed products or services. This is intended as a general guide to the job duties for this position and is intended for the purpose of establishing the specific salary grade. It is not designed to contain or be interpreted as an exhaustive summary of all responsibilities, duties and effort required of employees assigned to this job. At the discretion of management, this description may be changed at any time to address the evolving needs of the organization. Posting Dates: July 2, 2025 - July 17, 2025 Caterpillar is an Equal Opportunity Employer. Not ready to applyJoin our Talent Community.

Development & Qualification of multiplex based cytokine release assay and Elispot/ flow cytometry based T cell assays to measure the innate and adaptive Immunogenicity of synthetic peptide products Job Responsibilities Manage the study sample analysis for pipeline products, preparation of study schedule, design of experiments, trouble shooting, data analysis and review of reports. Isolation of PBMC from whole blood and maintenance of commercial cell lines. Coordinate with internal and external stakeholders for reagent procurement, blood collection, instrument installation and calibration. Statistical analysis of data using software. Preparation/ review of standard operating procedures (SOP), method development reports (MDR), sample analysis report (SAR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. Responsible for the operation and maintenance of the Flow Cytometry, Multiplex, ELISPOT and other instruments and statistical software. Managing of chemicals, consumables & critical reagents inventory. Performing calibration of instruments and equipment. Troubleshooting instrument performance and equipment issues. Draft responses for regulatory queries and facilitate internal and external audits.

Key Responsibilities The candidate is expected to develop LC-MS based methods for protein and peptide product characterization. The candidate is expected to qualify the methods for intended purpose for all pipeline products. The candidate is expected to design and implement integrated strategies, linking appropriate chromatography and mass spectrometry tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on LC-MS, CEX-MS, SEC-MS Characterization of innovator product batches sourced from different geographical region and preparation of quality target profile. Responsible for designing advance workflows such as multi-attribute methods for PTMs, sequence variants, qualitative and quantitative profiling of HCPs, Disulfide shuffling and bond analysis, cell culture metabolite analysis, glycan analysis etc. Preparation and review of method development reports (MDR) and analytical test procedures (ATP). Responsible for operating and maintaining analytical laboratory in compliance with GLP regulations. The candidate is responsible for the operation and maintenance of the MS instruments To manage chemicals,consumables & critical reagents inventory. Performs calibration of instruments and equipment. Troubleshoots instrument performance and equipment issues. Responsible for managing the regulatory queries. The candidate is expected to draft the technical content for regulatory dossier. Educational Qualification M.SC./M.Tech in Biochemistry / Life Sciences / Biotechnology. Technical/functional Skills Sound knowledge of analytical method development, qualification and structural and functional characterization of therapeutic proteins. Experience of biosimilarity assessment of biologics for regulated market is desirable. Experience of analytical development for monoclonal antibodies and fusion proteins and peptide is highly desirable.