Our Story
The life sciences industry despite its incredible innovation continues to face complex, high-stakes challenges that demand not just technical knowledge, but trusted, real-world expertise. In 2025, after years of working on the frontlines of biotech, pharmaceuticals, and medical devices, seasoned industry professionals came together with a shared vision. They had each seen the critical gaps that can derail projects due to lack of compliance clarity, inefficient processes, and siloed project teams. They knew there had to be a better way to support life sciences companies in building safe, compliant, and efficient operations.That vision became CellSpark Consulting: a consultancy built by experienced and passionate professionals for industry innovators. We set out to become more than just advisors, we became true partners to our clients. From emerging biotechs launching their first facility, to global pharma firms managing complex technology transfers; CellSpark aspire to be a trusted name in life sciences consulting.
What sets CellSpark apart isn’t just what we do, but it’s how we do it. We approach every project with the mindset of ownership, collaboration, and excellence. We don’t believe in one-size-fits-all solutions; we craft tailored strategies aligned with your stage, goals, and regulatory landscape. Today, CellSpark Consulting stands at the intersection of science, compliance, and innovation, helping our clients bring life-changing therapies to market faster, safer, and smarter.
Let us help spark the next breakthrough in your journey.
Our Purpose & Aspiration
At CellSpark Consulting, our purpose is to empower our partners to deliver safe, effective, and compliant therapies to patients faster and smarter. We do this by providing expert guidance in validation, regulatory compliance strategy, technology transfer, and post-transfer integration and process optimization. Grounded in real-world industry experience and a commitment to excellence, we help our industry partners achieve operational excellence and effortless regulatory compliance.
We aspire to be a trusted partner for biotech and pharmaceutical companies globally, known for precision, reliability, and forward-thinking strategy.
Our goal is to empower life sciences companies, ranging from agile startups to global pharmaceutical leaders, to achieve operational excellence, regulatory compliance, and sustainable growth. Support the advancement of life-saving technologies through application of advanced technologies, data-driven insights, and interdisciplinary approaches to solve complex scientific problems more efficiently and innovatively. Build a team of trusted advisors that not only solves problems, but anticipates them, igniting continuous improvement across the life sciences ecosystem.
Our Core Strengths
Transparency
Transparent communication and partnership-driven approach to align with client goals and timelines. We apply risk-based strategies to ensure compliance, efficiency, and long-term success.
Agile Consulting Model
We have an Agile consulting model to deliver flexible, iterative, and client-focused solutions that adapt to evolving project needs and regulatory demands.
Deep Domain Expertise
Decades of combined experience in life sciences research, biotech, pharma, and regenerative medicine
End-to-End Project Support
Comprehensive services from early-phase development to GMP manufacturing and post-market compliance.
Technical Leadership
Expertise in CSV, CQV, Quality Assurance, and Process Development tailored to complex, evolving technologies.
Regulatory Excellence
Proven track record navigating global regulatory frameworks (GMP, GAMP, FDA, EMA, ICH) with confidence.
Global Perspective
Cross-functional experience across North America and Asia in both operational and scientific roles.
Meet the Team
Seema Das, PhD
Founder & Principal Consultant
Seema is a subject matter expert in GMP manufacturing operations with extensive experience in Quality & Compliance, and scientific research across North America and Asia. She led complex GMP operations, in CGT manufacturing space, and supported operations for manufacturing clinical stage products for stakeholders like BlueRock Therapeutics, Nkarta Inc, panCELLA, Sigilon Therapeutics, Notch Therapeutics, and The Hospital for Sick Children.
Seema holds a PhD in Biological Science and her strong scientific foundation is rooted in advanced academic research, including postdoctoral work in bloodborne infectious diseases and CNS HIV at University of Texas Medical Branch and the National University of Singapore. This deep understanding of life sciences complements her industry expertise, enabling a unique perspective that bridges science, compliance, and operational strategy.
Shubhajit Mitra, PhD
Co-Founder & Principal Consultant
Shubhajit leads with a vision to position the firm as a trusted partner in GMP compliance, validation, and digital transformation. He defines long-term strategy, oversees client delivery, and champions modern, risk-based solutions across pharma, biotech, and advanced therapy sectors. Shubh fosters strategic partnerships, mentors a high-performing consultant network, and integrates agile project management and digital tools to drive operational excellence and regulatory alignment.
Shubhajit holds a PhD in biological sciences, with postdoctoral research in epigenetic regulation during host-pathogen interactions, contributing to NIH-funded research and publication. He is a certified PMP and PMI-ACP with additional training in data science and AI, bringing an agile, digitally fluent approach to quality and regulatory strategy. His blend of scientific depth and operational insight underpins CellSpark Consulting’s mission to bridge the gap between compliance, innovation, and execution.
Arun Pandey
Advisory Board Member
Arun brings a wealth of entrepreneurial experience and a proven track record that will be invaluable. In his role, he'll be directly involved in shaping our strategic growth initiatives, sharpening our go-to-market strategies, and meticulously planning our long-term market positioning. Our goal is clear: to be a front-runner in the dynamic life science consulting landscape, and Arun will be key to that success
Jagrut Parikh
Operations Advisor
Jagrut is a seasoned quality and validation expert with over 10 years of experience in GMP compliance, thermal mapping, and pharmaceutical manufacturing. He has supported global clients through his key roles at PharmEng, Phoena, and Teva. At CellSpark, Jagrut plays a central role in guiding clients through the development and implementation of robust, audit-ready GxP solutions. He brings deep expertise in validation, quality systems, and environmental qualification, helping organizations strengthen compliance, streamline operations, and maintain inspection readiness across regulated environments.
Focus Areas: GMP Compliance, QA, Validation, Thermal Mapping, Audit Support