Aditya Jarare
Research and Development Manager @Beckman Coulter Life Sciences
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WORK HISTORY
Research and Development Manager @Beckman Coulter Life Sciences
Bengaluru, IN
Directed the full lifecycle of IVD reagent kit development for flow cytometry, from proof-of-concept through feasibility, characterization, verification, and regulatory submission, ensuring successful FDA and CE-IVD approvals.Managed and engaged a global team of 60 associates from various functions, cross-functional stakeholders (directly and indirectly), driving alignment across sites in North America, Europe, Africa, China, and India to deliver products to market.Championed team engagement initiatives — structured workshops, technical reviews, and collaborative problem-solving sessions — to foster ownership, accountability, and innovation across diverse teams.Established and executed R&D strategy, balancing technical innovation with operational discipline to accelerate timelines and reduce risk.Implemented robust risk management frameworks (Design FMEA, system risk assessments), minimizing project delays and ensuring compliance with ISO and FDA design control standards.Partnered with manufacturing and quality teams to streamline tech transfer, reducing scale-up bottlenecks and enabling faster commercialization of diagnostic products.Leveraged advanced data analysis tools (FlowJo, JMP, GraphPad) to optimize assay performance, stability studies, and decision-making processes.Served as independent technical reviewer for multiple global projects, ensuring deliverables met organizational guidelines and regulatory expectations.Recognized for innovation and leadership excellence, including patent contributions and organizational awards, reinforcing Beckman Coulter’s reputation in diagnostic product development.
EDUCATION
Devi Ahilya Vishwavidyalaya
B.Sc. Biotechnology, Biotechnology
Birla Institute of Technology and Science, Pilani
M.Tech. Quality Management
Nagpur University
M.Sc. Biotechnology, Biotechnology
SKILLS
ABOUT ADITYA JARARE
My expertise spans formulation development, immunoassays, and system qualification of reagents and instruments, ensuring compliance with global regulatory standards. I thrive at the intersection of science and strategy — leading cross-functional teams, mitigating risks, and accelerating timelines to deliver high-impact healthcare solutions.
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