The Laboratory Systems Consultant is responsible for supporting the implementation, validation, and ongoing delivery of laboratory informatics systems such as Electronic Laboratory Notebooks (ELN) and Laboratory Information Management Systems (LIMS) within a regulated pharmaceutical or biopharmaceutical workplace. This role focuses on writing and executing User Acceptance Testing (UAT) and validation test scripts, performing unit testing for each sprint release, and translating laboratory and business needs into clear, traceable system requirements. The consultant will work closely with laboratory stakeholders, IT, quality teams, and vendors to ensure system quality, compliance, and successful adoption.

Essential Functions:

- Support the implementation, configuration, and enhancement of laboratory systems, including Electronic Laboratory Notebooks (ELN) and Laboratory Information Management Systems (LIMS).
- Author User Acceptance Testing (UAT) protocols, validation test scripts, and related documentation in compliance with GxP requirements.
- Execute UAT, validation, and regression test scripts and document results, deviations, and remediation efforts.
- Perform unit testing for each sprint release within an Agile development environment.
- Gather, analyze, and document business and laboratory requirements.
- Maintain traceability between system requirements, test cases, and validation deliverables.
- Collaborate with laboratory users, IT teams, quality, and system vendors to ensure successful system delivery and adoption.
- Support issue resolution, defect tracking, and system readiness for production release.





Necessary Skills and Abilities:

- Strong knowledge of computerized system validation (CSV) in regulated pharmaceutical environments.
- Working knowledge of laboratory systems, including:
- Electronic Laboratory Notebooks (ELN)
- Laboratory Information Management Systems (LIMS)
- Laboratory Execution Systems (LES) / Manufacturing Execution Systems (MES)
- Electronic Quality Management Systems (eQMS)

- Ability to write clear, detailed requirements, test scripts, and validation documentation.
- Experience working within Agile or Scrum-based delivery models.
- Strong analytical, problem-solving, and organizational skills.
- Effective communication skills with the ability to work across scientific, technical, and quality teams.
- High attention to detail and commitment to data integrity and compliance.

Educational Requirements:

- Minimum B.S./B.A. in a scientific discipline (e.g., Biology, Chemistry, Biochemistry, Engineering, Computer Science or related field)

Experience Requirements:

- Minimum 5 years of experience in the Pharmaceutical or Biopharmaceutical industry.
- Proven experience supporting laboratory informatics systems and validation activities.
- Hands-on experience working in a laboratory setting is preferred.
- Prior experience writing and executing UAT and validation test scripts in a regulated environment.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

📌 Laboratory Systems Consultant (Hyderabad)
🏢 Propharma Group
📍 Hyderabad