Job Summary
Experience:
5.00 - 8.00 Years
Industrial Type:
Medical/Healthcare/Hospital
Location:
Bangalore
Functional Area:
IT Software - Other
Designation:
Senior Lead/ Senior Manager
Key Skills:
Program Manager
Educational Level:
Graduate/Bachelors
Job Post Date:
2026-10-30
Stream of Study:
Engineering
Degree:
BE-Comp/IT
Company Description
Our client is a platform-first biotech company pioneering fast, scalable, and accessible CRISPR-based solutions. They translate cutting-edge gene technologies into powerful tools for diagnostics, disease screening, and genome engineering, designed not just for advanced laboratories, but for any setting where they are needed most. They reimagine what CRISPR can do by engineering it to work faster, more economically, and without dependence on heavy infrastructure. Our platforms are modular, programmable, and optimized for real-world deployment, from remote clinics to research labs and field environments.
Job Description
Key Responsibilities:
• Own the diagnostics pipeline end-to-end—timelines, milestones, risks, and resources from feasibility to launch.
• Drive IVD kits through design transfer, verification and validation, and regulatory filings (CDSCO, CE-IVDR).
• Build external partnerships with hospitals, labs, and KOLs to secure samples, run validations, demos, and studies.
• Design and manage performance studies—protocols, site coordination, data analysis, and reports.
• Coordinate across R&D, Manufacturing, QA/RA, and Commercial to clear bottlenecks and speed up decisions.
• Build dashboards on pipeline status, timelines, and cost; flag risks early.
• Run program reviews and prepare updates for leadership, partners, and funders.
Qualifications:
• Science background (must have): Bachelor’s or above in life sciences, biotechnology, or molecular biology; Master’s or PhD preferred
• 5 - 8 years’ experience in molecular diagnostics kit development (IVD) and launch across Indian (CDSCO) and European (CE-IVD/IVDR) pathways is a MUST
• Project management experience running multi-stakeholder programs to deadline in diagnostics or life sciences is a MUST
• Working knowledge of clinical performance studies and ISO 13485 quality systems will be an added advantage
• Excellent analytical skills; comfortable with data, timelines, and trade-offs
• Confident in partner-facing roles; network with hospitals, labs, or CROs a plus
• PMP certification will be an added advantage
