Key Responsibilities

- Regulatory documentation: Prepare, compile, review, and maintain regulatory dossiers, submissions, applications, and supporting documents as per applicable requirements.

- Regulatory compliance: Monitor relevant regulatory guidelines, notifications, standards, and compliance requirements and support their implementation within the organization.

- Cross-functional coordination: Coordinate with R&D;, quality assurance, quality control, clinical/preclinical, manufacturing, and other teams to collect and review information required for regulatory submissions.

About Company: Technoculture Research is reimagining how the world measures health by building micro-scale electrochemical laboratories that deliver lab-grade accuracy directly into the hands of clinicians, community health workers, and even patients at home.



The platform integrates microfabricated electrodes, advanced surface chemistries, and microfluidics to enable rapid protein, nucleic-acid, and metabolite assays within minutes. By replacing expensive optical detection methods with electron sensing, the company significantly reduces both instrument and per-test costs- often by an order of magnitude- making precision diagnostics more accessible and scalable.

With a explicit mission to make diagnostics abundant, Technoculture Research aims to ensure that every critical health decision is supported by immediate, affordable, and reliable results, regardless of where care is delivered.

📌 Regulatory Affairs Associate in Bodhgaya (Bodh Gaya)
🏢 Technoculture Research
📍 Bodh Gaya