As a Senior Software Engineer Backend (Python) at our company, you will play a crucial role in developing scalable, high-performance backend systems for the life sciences and healthcare technology industry. You will leverage your expertise in Python to build robust backend systems, integrate with front-end applications, and contribute to our cloud infrastructure and data platforms. Your key responsibilities will include designing, developing, and maintaining backend systems and APIs using Python. You will work on full-stack solutions, utilizing Node.js and React for occasional front-end tasks. Deploying, monitoring, and managing cloud-native applications using AWS services such as EC2, Lambda, S3, and CloudWatch will be part of your daily tasks. You will also be responsible for developing and optimizing complex SQL queries to ensure efficient interaction with relational databases. Collaboration is key in this role, as you will work closely with cross-functional teams including product, data, and QA to deliver secure, compliant, and scalable solutions. Your expertise in RESTful API design, microservices architecture, and system integration patterns will be essential. Additionally, you will apply agile development methodologies, participate in sprint planning, and contribute to team retrospectives. Maintaining high standards for code quality, testing, and documentation is also a critical aspect of this role. To be successful in this position, you should possess a Bachelor's or Master's degree in Computer Science, Engineering, or a related field, along with at least 6 years of experience in backend development using Python. Strong hands-on experience with AWS and deploying applications in a cloud-native environment is required. Proficiency in Node.js and React, expertise in relational databases like PostgreSQL and MySQL, and experience with version control systems like Git are also necessary. If you have experience working in regulated industries or life sciences/healthcare technology platforms, familiarity with compliance standards such as HIPAA and GxP, or exposure to data integration tools and bioinformatics workflows, it would be considered a plus. Join our team to contribute to meaningful technology in the life sciences domain, work with a collaborative and innovative team, enjoy competitive compensation and benefits, and benefit from flexible working arrangements and growth opportunities.,
Job Title: Director of Regulatory Research & Intelligence Location: Hybrid (Hyderabad) Industry: Life Sciences / Healthcare Technology Experience Level: 10+ years Employment Type: Full-time About the Role As Director of Regulatory Research & Intelligence, you will lead and develop a team of research consultants responsible for regulatory intelligence, compliance support, and advisory services for clients across the pharmaceutical and medical device sectors. You will ensure delivery excellence, quality control, and strategic insight, serving as the senior-most authority for regulatory research activities in India. You will interface directly with global clients, executive stakeholders, and cross-regional project leads. Core Responsibilities · Team Leadership: Build, mentor, and oversee a multidisciplinary team of research consultants; set performance targets and foster professional development. · Quality Oversight: Ensure that all research, analysis, and regulatory intelligence delivered by the India team meets Kamet’s global quality and compliance standards. · Strategic Research Direction: Define and evolve the group’s research agenda in alignment with emerging regulatory trends (FDA, EMA, CDSCO, TGA, etc.) and client priorities. · Project Delivery: Oversee the execution of complex regulatory intelligence projects, ensuring on-time and in-scope delivery. · Stakeholder Communication: Present complex regulatory insights, implications, and recommendations clearly and persuasively to executive audiences, both written and verbal, in English. · Cross-Functional Alignment: Collaborate with consultants and subject matter experts in regulatory affairs, clinical, quality, supply chain, labeling, and M&A. · Risk Management: Identify and mitigate regulatory and reputational risks for client organizations. · Continuous Improvement: Implement best practices, tools, and methodologies to enhance team capability and operational efficiency. Required Qualifications · Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field. PhD or MBA preferred. RAC or equivalent certification is a plus. · Experience: 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices; at least 5 years in consulting, including direct client-facing roles and team management. · Leadership: Demonstrated track record of leading research or regulatory teams (preferably in an international or cross-functional environment). · Regulatory Depth: Expert knowledge of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, etc.), GMP/GCP/QMS. · Communication: Exceptional verbal and written English skills; able to convey nuanced regulatory insights to senior stakeholders and non-experts alike. · Project Management: Experience overseeing multiple concurrent projects and managing project managers/consultants. · Analytical Skills: Advanced research, data analysis, and reporting capabilities, including proficiency in regulatory databases and business tools (Excel, PowerPoint, relevant software). · Entrepreneurial Mindset: Ability to drive innovation, efficiency, and value in a rapidly evolving regulatory landscape. Desired Traits · Well-read on regulatory and scientific literature; ability to synthesize new research and guide the team on best practices. · Culturally adept, able to operate and lead in global teams. · High ethical standards and a passion for quality in research and client service. About Kamet Consulting Group Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply. Why Join Us Contribute to meaningful technology in the life sciences domain. Work with a collaborative, forward-thinking team committed to innovation. Competitive compensation and benefits package. Flexible working arrangements and growth opportunities.
As the Director of Regulatory Research & Intelligence at Kamet Consulting Group, you will be responsible for leading and developing a team of research consultants in the life sciences and healthcare technology industry. Your role will involve overseeing regulatory intelligence, compliance support, and advisory services for clients in the pharmaceutical and medical device sectors. You will be the key authority for regulatory research activities in India, ensuring delivery excellence, quality control, and strategic insights. Your core responsibilities will include building and mentoring a team of research consultants, setting performance targets, and fostering their professional development. You will also be responsible for ensuring that all research, analysis, and regulatory intelligence meets global quality and compliance standards. Additionally, you will define and evolve the research agenda in alignment with regulatory trends and client priorities, oversee project delivery, and communicate complex regulatory insights to executive audiences. To qualify for this role, you should have an advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or a related field, with a preference for a PhD or MBA. You should have at least 10 years of experience in regulatory affairs, regulatory intelligence, or compliance within the pharma/medical devices industry, including 5 years in consulting and team management roles. Strong leadership skills, expert knowledge of global and Indian regulatory frameworks, exceptional communication abilities, project management experience, and an entrepreneurial mindset are essential for this position. Desired traits for the role include being well-read on regulatory and scientific literature, culturally adept in global teams, and having high ethical standards and a passion for quality in research and client service. Kamet Consulting Group offers a collaborative and innovative work environment, competitive compensation and benefits package, flexible working arrangements, and growth opportunities for all qualified applicants. Join us to contribute to meaningful technology in the life sciences domain and be part of a team committed to innovation.,
Job Title: Global Regulatory HR Lead Location: Hybrid (Hyderabad) Industry: Life Sciences / Healthcare Technology Experience Level: 7+ years Employment Type: Full-time CTC :₹5,00,000 – ₹6,00,000 per annum About the Role We are seeking an accomplished Regulatory Affairs HR Manager to oversee the full spectrum of human resources operations for a rapidly scaling, high-performance consulting organization. The successful candidate will demonstrate exceptional leadership, possess a proven track record managing HR teams of 10 or more, and bring deep expertise in people management, compliance, and HR technology. The ideal candidate will be well-versed in the HR demands of the consulting, pharmaceutical, and regulated industries and exhibit outstanding verbal and written English communication skills. Key Responsibilities Lead, develop, and inspire a geographically dispersed HR team of 10+ professionals, ensuring alignment with Kamet’s mission and values. Build a culture of high performance, accountability, and continuous improvement. Work closely with the Chief of Staff and global leadership to integrate HR practices across regions. Direct all aspects of the recruitment lifecycle, from workforce planning to talent sourcing, selection, and onboarding. Collaborate with business leaders to forecast talent needs and attract best-in-class candidates. Design and implement robust performance management frameworks, including goal-setting, appraisals, and development plans. Partner with functional leaders to identify high-potential talent and succession planning. Ensure full compliance with applicable labor laws, regulatory standards (e.g., GMP, GCP, QMS), and industry best practices. Develop, communicate, and enforce HR policies and SOPs that support regulatory intelligence, risk management, and ethical conduct. Liaise with cross-functional teams, including Regulatory Affairs, to align HR processes with business and compliance needs. Champion a positive and inclusive workplace culture, driving engagement, diversity, and well-being initiatives. Resolve employee concerns and conflicts promptly and professionally, ensuring fairness and consistency. Leverage HR analytics to track KPIs, monitor workforce trends, and inform data-driven decision-making. Identify skill gaps and work in locked step with global team on creating learning roadmaps, facilitating professional development and upskilling opportunities. Coordinate internal and external training aligned with regulatory and business requirements. Drive the adoption and optimization of HRIS and digital tools to streamline HR processes, reporting, and compliance documentation. Ensure accurate record-keeping and reporting in support of audits, regulatory submissions, and leadership reviews. Technical & Professional Competencies Compliance Acumen: Strong understanding of regulatory frameworks such as GMP, GCP, QMS, and the ability to translate regulatory updates into actionable HR policies. Documentation & Communication: Superior documentation, reporting, and presentation skills; fluent in written and spoken English with the ability to prepare high-quality reports for leadership. Project Management: Proficient in managing multiple HR projects in parallel, including M&A due diligence, workforce integration, and compliance audits. Proficiency with Office Suite: Advanced skills in MS Office (Word, Excel, PowerPoint), and familiarity with collaboration tools such as Microsoft Teams and SharePoint. Required Qualifications Graduate or postgraduate degree in Human Resources, Business Administration, or related discipline. Minimum 5 years of progressive HR experience, including at least 3 years managing HR teams of 10 or more. Experience in life sciences, consulting, or highly regulated environments preferred. Professional certification (SHRM, CIPD, PHR, HRCI) is highly desirable. Why Join Us Build meaningful technology solutions that advance the life sciences and healthcare domain . Work in a collaborative, high-caliber engineering team focused on innovation and quality. Competitive compensation and benefits. Flexible work culture with opportunities for growth and learning.
Job Title: UI/UX Designer Location: Hybric (Hyderabad) Industry: Life Sciences / Healthcare Technology Experience Level: 5+ years Employment Type: Full-time (Immediate Joiners) We are seeking a UI/UX Designer with a strong background in creating intuitive, user-centered digital experiences for complex applications. Ideal candidates will have direct experience in the life sciences industry , along with a solid understanding of modern design systems and accessibility standards. This role involves designing user interfaces for healthcare platforms, collaborating with development teams, and ensuring compliance with industry regulations. Key Responsibilities Design and prototype user interfaces for web and mobile applications using industry-standard design tools. Conduct user research, create user personas, and develop user journey maps to inform design decisions. Collaborate closely with backend and frontend developers to ensure seamless implementation of designs. Create and maintain design systems and component libraries to ensure consistency across products. Design responsive interfaces that work across various devices and screen sizes. Apply user-centered design principles and conduct usability testing to validate design solutions. Ensure designs meet accessibility standards (WCAG 2.1) and comply with healthcare industry regulations. Participate in agile development processes, including sprint planning, design reviews, and stakeholder presentations. Create wireframes, mockups, interactive prototypes, and detailed design specifications. Collaborate with cross-functional teams, including product, engineering, and QA to deliver compliant and user-friendly solutions. Required Qualifications Bachelor's or Master's degree in Design, Human-Computer Interaction, or a related field. 4+ years of experience in UI/UX design for web and mobile applications. Strong portfolio demonstrating expertise in user interface design and user experience research. Proficiency in design tools such as Figma, Adobe Creative Suite, Sketch, or similar platforms. Experience with prototyping tools (e.g., Figma, InVision, Adobe XD) and creating interactive mockups. Solid understanding of responsive design principles and mobile-first design approaches. Knowledge of HTML/CSS fundamentals to effectively communicate with development teams. Experience with design systems and component-based design methodologies. Understanding of agile methodologies (Scrum, Kanban) and collaborative design processes. Preferred Qualifications Experience working with regulated industries or life sciences / healthcare technology platforms. Familiarity with HIPAA, accessibility compliance (Section 508, WCAG), or other relevant regulatory standards. Experience with user research methodologies, including interviews, surveys, and usability testing. Knowledge of data visualization and designing for complex scientific or medical data. Understanding of healthcare workflows and clinical user needs is a plus. Why Join Us Contribute to meaningful technology in the life sciences domain. Work with a collaborative, forward-thinking team committed to innovation. Competitive compensation and benefits package. Flexible working arrangements and growth opportunities.
Ideal Candidate is an Immediate Hire [Hiring for Multiple Positions] Job Description: It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. We are looking to fill multiple open roles for Associate Manager through Senior Regulatory Affairs / Regulatory Intelligence Lead (Pharmaceutical and Medical Devices) specializing in Pharmaceuticals and Medical Devices supporting monitoring, analyzing, and interpreting regulatory changes and developments within the pharmaceutical and medical device industries. This position involves staying abreast of evolving regulatory requirements, guidelines, and standards to ensure compliance and mitigate regulatory risks for the organization. This is an exciting opportunity to work within our management consulting directly interacting with customers to build bespoke solutions to solve their business problems. The candidate will collaborate with our content matter experts and consultants while gaining a detailed understanding of internal and external data sets (e.g., registrations data, health authority correspondence, regulatory intelligence, etc.) Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. Our expertise spans across organizational and functional areas of Deals, R&D, Clinical, Regulatory, Quality, Labeling, Safety, Supply Chain, and Commercial. We pride ourselves in bringing extensive experience and professionalism to every engagement and customize our support to our client’s individual needs and opportunities. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. At Kamet Consulting Group, we strive to create a strong and inclusive workforce by actively seeking a diverse pool of applicants. We firmly believe in providing equal opportunities to all qualified candidates, without any discrimination based on factors such as race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Responsibilities Monitor Regulatory Landscape: Stay updated on regulatory changes, trends, and developments specific to the pharmaceutical and medical device industries. Conduct Research: Research and analyze regulatory requirements, guidelines, and policies issued by regulatory authorities, such as the FDA (Food and Drug Administration), EMA (European Medicines Agency), and other relevant agencies worldwide. Assess Implications: Evaluate the potential impact of regulatory changes on pharmaceutical and medical device manufacturing, distribution, labeling, and marketing practices. Provide Insights and Analysis: Summarize and interpret regulatory information to provide actionable insights and recommendations to internal stakeholders, including regulatory affairs teams, compliance officers, and product development teams. Regulatory Compliance Support: Collaborate with cross-functional teams to ensure understanding and compliance with applicable regulations and requirements governing pharmaceutical and medical device products. Risk Assessment: Identify regulatory risks and vulnerabilities related to product development, manufacturing processes, and post-market surveillance. Propose strategies to address and mitigate regulatory risks effectively. Documentation and Reporting: Maintain accurate records of regulatory updates, analysis reports, and compliance documentation specific to pharmaceutical and medical device regulations. Prepare and present regulatory intelligence reports as needed. Stay Informed: Continuously monitor industry best practices, emerging trends, and regulatory enforcement actions relevant to pharmaceuticals and medical devices. Provide training and updates to internal stakeholders as necessary. Qualifications and Skills: Bachelor's degree in Pharmacy, Life Sciences, Regulatory Affairs, or a related field. Advanced degree or professional certification (e.g., RAC - Regulatory Affairs Certification) is preferred. Proven experience (typically 2-5 years) in regulatory affairs, regulatory compliance, or a related role within the pharmaceutical or medical device industry. Strong understanding of regulatory frameworks, laws, and compliance requirements governing pharmaceuticals and medical devices, including Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and Quality Management Systems (QMS). Excellent research, analytical, and critical thinking skills with the ability to interpret complex regulatory information and assess its implications for product development and commercialization. Detail-oriented with strong organizational and documentation skills. Effective communication skills, both written and verbal, with the ability to convey regulatory insights and recommendations to diverse stakeholders. Ability to work independently, prioritize tasks, and meet deadlines in a fast-paced, highly regulated environment. Proficiency in utilizing regulatory databases, research tools, and software applications for data analysis and reporting. Other skills Consulting experience with an ability to interface directly with clients Ability to work in an agile environment and critical thinking while working with customers to deliver the final solution Adept at conducting research Competencies with Powerpoint and advanced Excel Self motivated Required Qualifications: Advanced degree preferred Minimum of 4-6 years of work experience related within the pharmaceutical and/or medical device industry Prior lifesciences consulting experience especially leading projects within M&A, Regulatory Affairs, Labeling, and Supply Chain is preferred Benefits: Competitive salary and benefits package Opportunity to work on groundbreaking projects with Top Organizations Professional development and growth opportunities. Hybrid work options How to Apply: We thank all applicants for their interest; however, only those selected for an interview will be contacted.
Job Title: Sr. Software Engineer – Frontend (React/JavaScript) Location: Hybrid (Hyderabad) Industry: Life Sciences / Healthcare Technology Experience Level: 6+ years Employment Type: Full-time About the Role We are seeking a Senior Software Engineer – Frontend (React/JavaScript) with a strong background in building responsive, scalable, and accessible user interfaces. Ideal candidates will have experience in the life sciences or healthcare technology domain and a solid grasp of modern frontend engineering practices. This role involves developing advanced frontend features, collaborating with backend and design teams, and ensuring seamless user experiences across devices and platforms. Key Responsibilities Design, develop, and maintain robust, modular, and scalable frontend applications using React and JavaScript/TypeScript . Collaborate with backend engineers to integrate RESTful APIs and microservices into user-facing applications. Translate complex user requirements and UI/UX designs into elegant and functional user interfaces. Ensure cross-browser compatibility, responsive design, and accessibility (WCAG) compliance. Optimize frontend performance through lazy loading, code splitting, and other best practices. Work closely with product managers, designers, and QA engineers to deliver high-quality features through agile sprints. Maintain high standards for code quality , testing (e.g., Jest, React Testing Library), and documentation . Participate in peer code reviews and contribute to frontend-focused CI/CD pipelines. Required Qualifications Bachelor’s or Master’s degree in Computer Science, Engineering, or a related technical field. 6+ years of professional frontend development experience with React and JavaScript/TypeScript. Extensive knowledge of component-driven architecture, state management (Redux, Zustand, React Context), and frontend build tools (Webpack, Vite, Babel). Proven experience integrating RESTful APIs and working effectively within microservices-based systems. Proficiency in HTML5, CSS3, SCSS, and responsive UI frameworks (Tailwind CSS, Material UI). Expertise with version control systems (Git) and CI/CD processes (GitHub Actions, CircleCI). Familiarity with agile development methodologies (Scrum, Kanban) and frontend performance optimization. Strong skills in unit and integration testing (Jest, React Testing Library), ensuring high code quality and maintainability. Commitment to cross-browser compatibility, responsive and mobile-first design, and accessibility standards compliance (WCAG). Preferred Qualifications Experience in regulated industries, specifically life sciences or healthcare technology. Knowledge of industry compliance standards such as HIPAA, GxP, or related regulations. Exposure to design systems, accessibility frameworks, and data-intensive dashboard applications. Why Join Us Build meaningful technology solutions that advance the life sciences and healthcare domain . Work in a collaborative, high-caliber engineering team focused on innovation and quality. Competitive compensation and benefits. Flexible work culture with opportunities for growth and learning.
Job Title: Senior Software Engineer – Backend (Python) Location: Hybrid (Hyderabad) Industry: Life Sciences / Healthcare Technology Experience Level: 6+ years Employment Type: Full-time About the Role We are seeking a Senior Software Engineer – Backend (Python) with a strong background in developing scalable, high-performance backend systems. Ideal candidates will have direct experience in the life sciences industry , along with a solid understanding of modern cloud-native development practices. This role involves building robust backend systems, integrating with front-end applications, and contributing to our cloud infrastructure and data platforms. Key Responsibilities Design, develop, and maintain backend systems and APIs using Python. Work on full-stack solutions, contributing to both backend and occasional front-end tasks using Node.js and React . Deploy, monitor, and manage cloud-native applications using AWS services (e.g., EC2, Lambda, S3, CloudWatch). Develop and optimize complex SQL queries and ensure efficient interaction with relational databases . Collaborate with cross-functional teams including product, data, and QA to deliver secure, compliant, and scalable solutions. Apply agile development methodologies , participate in sprint planning, and actively contribute to team retrospectives. Maintain high standards for code quality , testing, and documentation. Participate in code reviews and contribute to continuous integration and continuous deployment (CI/CD) pipelines. Required Qualifications Bachelor’s or Master’s degree in Computer Science, Engineering, or a related field. 6+ years of experience in backend development using Python . Strong hands-on experience with AWS and deploying applications in a cloud-native environment . Solid understanding of RESTful API design , microservices architecture, and system integration patterns. Proficiency in Node.js and React , especially in full-stack project environments. Strong expertise in relational databases (e.g., PostgreSQL, MySQL) and complex SQL query writing . Experience with version control systems like Git, and tools for CI/CD (e.g., Jenkins, GitHub Actions). Understanding of agile methodologies (Scrum, Kanban) and modern DevOps practices. Preferred Qualifications Experience working with regulated industries or life sciences / healthcare technology platforms. Familiarity with HIPAA, GxP, or other relevant compliance standards. Exposure to data integration tools or bioinformatics workflows is a plus. Why Join Us Contribute to meaningful technology in the life sciences domain. Work with a collaborative, forward-thinking team committed to innovation. Competitive compensation and benefits package. Flexible working arrangements and growth opportunities.
Job description Ideal Candidate is an Immediate Hire [Hiring for Multiple Positions] Job Description: It's an exciting time to join Kamet Consulting Group as we continue our hyper growth journey. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. We are looking to fill multiple open roles for Associate Manager through Senior Regulatory Affairs / Regulatory Intelligence Lead (Pharmaceutical and Medical Devices) specializing in Pharmaceuticals and Medical Devices supporting monitoring, analyzing, and interpreting regulatory changes and developments within the pharmaceutical and medical device industries. This position involves staying abreast of evolving regulatory requirements, guidelines, and standards to ensure compliance and mitigate regulatory risks for the organization. This is an exciting opportunity to work within our management consulting directly interacting with customers to build bespoke solutions to solve their business problems. The candidate will collaborate with our content matter experts and consultants while gaining a detailed understanding of internal and external data sets (e.g., registrations data, health authority correspondence, regulatory intelligence, etc.) Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. Our expertise spans across organizational and functional areas of Deals, R&D, Clinical, Regulatory, Quality, Labeling, Safety, Supply Chain, and Commercial. We pride ourselves in bringing extensive experience and professionalism to every engagement and customize our support to our client’s individual needs and opportunities. We encourage entrepreneurial culture, spirit, which empowers individuals to think creatively, take initiatives, and drive innovative solutions. At Kamet Consulting Group, we strive to create a strong and inclusive workforce by actively seeking a diverse pool of applicants. We firmly believe in providing equal opportunities to all qualified candidates, without any discrimination based on factors such as race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Responsibilities Monitor Regulatory Landscape: Stay updated on regulatory changes, trends, and developments specific to the pharmaceutical and medical device industries. Conduct Research: Research and analyze regulatory requirements, guidelines, and policies issued by regulatory authorities, such as the FDA (Food and Drug Administration), EMA (European Medicines Agency), and other relevant agencies worldwide. Assess Implications: Evaluate the potential impact of regulatory changes on pharmaceutical and medical device manufacturing, distribution, labeling, and marketing practices. Provide Insights and Analysis: Summarize and interpret regulatory information to provide actionable insights and recommendations to internal stakeholders, including regulatory affairs teams, compliance officers, and product development teams. Regulatory Compliance Support: Collaborate with cross-functional teams to ensure understanding and compliance with applicable regulations and requirements governing pharmaceutical and medical device products. Risk Assessment: Identify regulatory risks and vulnerabilities related to product development, manufacturing processes, and post-market surveillance. Propose strategies to address and mitigate regulatory risks effectively. Documentation and Reporting: Maintain accurate records of regulatory updates, analysis reports, and compliance documentation specific to pharmaceutical and medical device regulations. Prepare and present regulatory intelligence reports as needed. Stay Informed: Continuously monitor industry best practices, emerging trends, and regulatory enforcement actions relevant to pharmaceuticals and medical devices. Provide training and updates to internal stakeholders as necessary. Qualifications and Skills: Bachelor's degree in Pharmacy, Life Sciences, Regulatory Affairs, or a related field. Advanced degree or professional certification (e.g., RAC - Regulatory Affairs Certification) is preferred. Proven experience (typically 2-5 years) in regulatory affairs, regulatory compliance, or a related role within the pharmaceutical or medical device industry. Strong understanding of regulatory frameworks, laws, and compliance requirements governing pharmaceuticals and medical devices, including Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and Quality Management Systems (QMS). Excellent research, analytical, and critical thinking skills with the ability to interpret complex regulatory information and assess its implications for product development and commercialization. Detail-oriented with strong organizational and documentation skills. Effective communication skills, both written and verbal, with the ability to convey regulatory insights and recommendations to diverse stakeholders. Ability to work independently, prioritize tasks, and meet deadlines in a fast-paced, highly regulated environment. Proficiency in utilizing regulatory databases, research tools, and software applications for data analysis and reporting. Other skills Consulting experience with an ability to interface directly with clients Ability to work in an agile environment and critical thinking while working with customers to deliver the final solution Adept at conducting research Competencies with Powerpoint and advanced Excel Self motivated Required Qualifications: Advanced degree preferred Minimum of 4-6 years of work experience related within the pharmaceutical and/or medical device industry Prior lifesciences consulting experience especially leading projects within M&A, Regulatory Affairs, Labeling, and Supply Chain is preferred Benefits: Competitive salary and benefits package Opportunity to work on groundbreaking projects with Top Organizations Professional development and growth opportunities. Hybrid work options How to Apply: We thank all applicants for their interest; however, only those selected for an interview will be contacted. Industry Business Consulting and Services Employment Type Full-time
IT Security Specialist - Cybersecurity & Infrastructure Management Kamet Consulting Group Location: (Hybrid) Hyderabad Compensation: ₹10-15 LPA (Based on Experience) Employment Type: Full-time, Immediate Hire Required Position Overview We are seeking a dynamic IT Security Specialist to join our team and take ownership of our cybersecurity infrastructure and device management systems. This role is critical in protecting our proprietary product content and ensuring enterprise-grade security across all organizational touchpoints. The successful candidate will work extensively with Microsoft Intune, security solutions, and implement Zero Trust security architectures similar to Okta and Zscaler frameworks. Key Responsibilities Cybersecurity & Threat Protection Implement and maintain comprehensive cybersecurity protocols to safeguard proprietary product content and intellectual property Design and enforce Zero Trust security architectures following Zscaler and Okta security models Monitor, analyze, and respond to security threats and incidents in real-time Conduct regular security assessments and vulnerability testing Develop and maintain incident response procedures and security documentation Microsoft Intune Device Management Deploy, configure, and manage Microsoft Intune for cross-platform device management (Windows, macOS, iOS, Android) Implement Mobile Device Management (MDM) and Mobile Application Management (MAM) policies Configure Conditional Access policies and device compliance requirements Manage device enrollment processes and user provisioning/de-provisioning Integrate Azure Active Directory for Single Sign-On (SSO) capabilities Cloud Security Implementation Configure and maintain Zscaler Internet Access (ZIA) and Zscaler Private Access (ZPA) Implement cloud firewall policies and network security controls Monitor network traffic and optimize security policies based on threat intelligence Manage user access controls and role-based permissions Coordinate with Zscaler support for escalated security incidents Infrastructure Security & Compliance Establish and maintain security policies for encryption, password requirements, and data protection Implement Data Loss Prevention (DLP) strategies for managed applications Ensure compliance with industry security standards and regulations Manage IP address allocation and network security configurations Conduct regular security audits and generate compliance reports Technical Support & Documentation Provide technical support for security-related issues and user access problems Create and maintain comprehensive documentation for all security configurations Develop user training materials and security awareness programs Collaborate with cross-functional teams to ensure security best practices Required Qualifications Technical Skills Bachelor's degree in Information Technology, Cybersecurity, Computer Science, or related field 1-3 years of experience in IT security, network administration, or related roles Hands-on experience with Microsoft Intune, Azure AD, and Microsoft 365 security features Knowledge of Zscaler ZIA/ZPA or similar cloud security platforms Understanding of Zero Trust security principles and implementation Experience with endpoint security, mobile device management, and cloud security Familiarity with network protocols, firewalls, and VPN technologies Security Expertise Strong understanding of cybersecurity frameworks and best practices Knowledge of threat detection, incident response, and vulnerability management Experience with compliance standards (ISO 27001, SOC 2, etc.) Understanding of encryption technologies and data protection methods Familiarity with SIEM tools and security monitoring platforms Professional Skills Strong analytical and problem-solving abilities Excellent communication and documentation skills Ability to work independently and manage multiple priorities Proactive approach to identifying and mitigating security risks Strong attention to detail and commitment to maintaining security standards Preferred Qualifications Relevant security certifications (Security+, CISSP, CEH, or similar) Experience with Okta identity management or similar IAM solutions Knowledge of PowerShell, Python, or other scripting languages Previous experience in a consulting or client-facing environment Understanding of DevSecOps practices and CI/CD security integration What We Offer Competitive salary package: ₹10-15 LPA based on experience and qualifications Opportunity to work with cutting-edge cybersecurity technologies Direct involvement in protecting critical business assets and intellectual property Professional development opportunities and certification support Collaborative work environment with experienced security professionals Immediate start opportunity for the right candidate Immediate Requirements This is an urgent hire - we need someone who can: Start immediately or within 2 weeks Take immediate ownership of our security infrastructure Quickly adapt to our existing Zscaler and Intune implementations Proactively identify and address security gaps Ready to protect what matters most? Apply now with your resume, relevant certifications, and a brief cover letter explaining your cybersecurity experience and why you're the right fit for this critical role. Application Deadline: Immediate consideration for qualified candidates Kamet Consulting Group is an equal opportunity employer committed to creating a diverse and inclusive workplace.
IT Security Specialist - Cybersecurity & Infrastructure Management Kamet Consulting Group Location: (Hybrid) Hyderabad Compensation: ₹10-15 LPA (Based on Experience) Employment Type: Full-time, Immediate Hire Required Position Overview We are seeking a dynamic IT Security Specialist to join our team and take ownership of our cybersecurity infrastructure and device management systems. This role is critical in protecting our proprietary product content and ensuring enterprise-grade security across all organizational touchpoints. The successful candidate will work extensively with Microsoft Intune, security solutions, and implement Zero Trust security architectures similar to Okta and Zscaler frameworks. Key Responsibilities Cybersecurity & Threat Protection Implement and maintain comprehensive cybersecurity protocols to safeguard proprietary product content and intellectual property Design and enforce Zero Trust security architectures following Zscaler and Okta security models Monitor, analyze, and respond to security threats and incidents in real-time Conduct regular security assessments and vulnerability testing Develop and maintain incident response procedures and security documentation Microsoft Intune Device Management Deploy, configure, and manage Microsoft Intune for cross-platform device management (Windows, macOS, iOS, Android) Implement Mobile Device Management (MDM) and Mobile Application Management (MAM) policies Configure Conditional Access policies and device compliance requirements Manage device enrollment processes and user provisioning/de-provisioning Integrate Azure Active Directory for Single Sign-On (SSO) capabilities Cloud Security Implementation Configure and maintain Zscaler Internet Access (ZIA) and Zscaler Private Access (ZPA) Implement cloud firewall policies and network security controls Monitor network traffic and optimize security policies based on threat intelligence Manage user access controls and role-based permissions Coordinate with Zscaler support for escalated security incidents Infrastructure Security & Compliance Establish and maintain security policies for encryption, password requirements, and data protection Implement Data Loss Prevention (DLP) strategies for managed applications Ensure compliance with industry security standards and regulations Manage IP address allocation and network security configurations Conduct regular security audits and generate compliance reports Technical Support & Documentation Provide technical support for security-related issues and user access problems Create and maintain comprehensive documentation for all security configurations Develop user training materials and security awareness programs Collaborate with cross-functional teams to ensure security best practices Required Qualifications Technical Skills Bachelor's degree in Information Technology, Cybersecurity, Computer Science, or related field 1-3 years of experience in IT security, network administration, or related roles Hands-on experience with Microsoft Intune, Azure AD, and Microsoft 365 security features Knowledge of Zscaler ZIA/ZPA or similar cloud security platforms Understanding of Zero Trust security principles and implementation Experience with endpoint security, mobile device management, and cloud security Familiarity with network protocols, firewalls, and VPN technologies Security Expertise Strong understanding of cybersecurity frameworks and best practices Knowledge of threat detection, incident response, and vulnerability management Experience with compliance standards (ISO 27001, SOC 2, etc.) Understanding of encryption technologies and data protection methods Familiarity with SIEM tools and security monitoring platforms Professional Skills Strong analytical and problem-solving abilities Excellent communication and documentation skills Ability to work independently and manage multiple priorities Proactive approach to identifying and mitigating security risks Strong attention to detail and commitment to maintaining security standards Preferred Qualifications Relevant security certifications (Security+, CISSP, CEH, or similar) Experience with Okta identity management or similar IAM solutions Knowledge of PowerShell, Python, or other scripting languages Previous experience in a consulting or client-facing environment Understanding of DevSecOps practices and CI/CD security integration What We Offer Competitive salary package: ₹10-15 LPA based on experience and qualifications Opportunity to work with cutting-edge cybersecurity technologies Direct involvement in protecting critical business assets and intellectual property Professional development opportunities and certification support Collaborative work environment with experienced security professionals Immediate start opportunity for the right candidate Immediate Requirements This is an urgent hire - we need someone who can: Start immediately or within 2 weeks Take immediate ownership of our security infrastructure Quickly adapt to our existing Zscaler and Intune implementations Proactively identify and address security gaps Ready to protect what matters most? Apply now with your resume, relevant certifications, and a brief cover letter explaining your cybersecurity experience and why you're the right fit for this critical role. Application Deadline: Immediate consideration for qualified candidates Kamet Consulting Group is an equal opportunity employer committed to creating a diverse and inclusive workplace.