Specialist, Material Management Tester
Core
Develop and execute test scripts for the Biovia OneLab-Biovia CISPro platform to support SDLC development and GMP validation in Quality Control labs.
Role type
Specialist, Material Management Tester (QA/Testing)
Builds
Custom software for global healthcare biopharma (prescription medicines, vaccines, animal health)
Domain
Healthcare biopharma / Regulated GxP environment
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Test plan and scenario creation, manual and automated software testing, defect documentation and reporting, regulatory compliance knowledge (FDA 21 CFR Part 11, data integrity), GxP environment experience, SDLC documentation
Preferred skills
Agile methodologies, Computer System Assurance (CSA), Laboratory Information Systems (LIMS), Laboratory Execution System (LES), Biovia CISPro
Technologies
Biovia OneLab, Biovia CISPro, LIMS, LES
Responsibilities
Create test plans, scenarios and test scripts; Implement software testing (manual, automated, exploratory); Document and report defects; Provide feedback to developers on usability and functionality; Support design of solutions complying with regulatory standards; Develop SDLC documents (SIT, UAT, test summaries)
Seniority
Specialist, 3-7 years experience
