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Business Analyst – Life Sciences (Product Development)

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Inductive Quotient Analytics

Degree in Life Sciences, Pharmacy, Biotechnology, MBBS, MBA or related fields

Hyderabad

1–3 years

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Inductive Quotient Analytics is hiring a Business Analyst – Life Sciences (Product Development) in Hyderabad. This is a high-impact, onsite role where you will drive requirement discovery, product documentation, and cross-functional alignment for a cutting-edge clinical platform. If you have hands-on experience in life sciences product development, BRD/FRD documentation, Jira/ADO, and clinical domain workflows, this opportunity offers strong career growth in the evolving healthcare technology space.


Key Responsibilities

  • Engage with product owners, SMEs, and clinical teams to gather and analyse business and functional requirements.
  • Prepare BRDs, FRDs, SRS documents, user stories, workflows, acceptance criteria, and process maps.
  • Support backlog refinement, sprint planning, and Agile/Scrum ceremonies.
  • Conduct gap analysis, impact analysis, and requirement prioritization.
  • Collaborate with Engineering, QA, and UI/UX teams to eliminate scope ambiguity.
  • Participate in UAT planning, test case review, execution, and defect triage.
  • Ensure alignment with industry standards such as GxP, ICH-GCP, 21 CFR Part 11, and compliance expectations.
  • Perform risk assessments related to functionality, compliance, data integrity, and product operations.
  • Recommend process improvements using as-is/to-be workflows.
  • Provide product demos, release documentation support, and training materials.
  • Maintain documentation hygiene, version control, and stakeholder communication.

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, MBBS, or related fields; MBA preferred.
  • 1–3 years of experience as a Business Analyst in life sciences product development.
  • Strong experience with user stories, acceptance criteria, Jira/ADO, and backlog management.
  • Proficiency in creating BRD/FRD/SRS, RTM, UAT documentation, and clinical workflows.
  • Knowledge of pharma R&D, clinical operations, data management, biostatistics, or regulatory processes.
  • Exposure to compliance frameworks: 21 CFR Part 11, HIPAA, GxP.
  • Strong communication, analytical thinking, and stakeholder management abilities.
  • Experience with Visio or similar process mapping tools.

Benefits

While the official benefits are not listed, typical advantages of working in life sciences product development include:

  • Growth in clinical technology and digital health ecosystems.
  • Exposure to cross-functional clinical teams and global product workflows.
  • Opportunity to build core expertise in regulatory-compliant product design.

How to Apply

Application Link

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