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.,