Review the quality of all materials at the site and ensure compliance with all project specifications, quality and collaborate with department for all material procurement.
Manage to lift all types of equipment and handle the efficient storage of all hazardous materials and perform quality audits as per requested.
Backend & API Validation: Perform backend testing, including data integrity validation, database querying (SQL), and API testing to ensure robust system integrations.
CI/CD Integration: Assist in integrating quality gates and automated test suites into the Continuous Integration/Continuous Deployment (CI/CD) pipelines.
Process Improvement: Participate actively in Agile/Scrum ceremonies, providing QA insights during sprint planning, and continuously refining the software development lifecycle (SDLC) to mitigate deployment risks.
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Review lot release data, identify testing discrepancies and participate in laboratory investigations.
Participate in inspection and ensure that the laboratory and documents are in a constant state of regulatory compliance and inspection readiness.
To assist in writing SOP documents, Change plan or change records (document revisions) supporting continuous improvement of test procedures and assay sheet design.
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Executes manufacturing operations to perform operations including but not limited to equipment cleaning and set up as well as stream specific operations like:Upstream: Vial Thaw, Inoculation, Cell Culture and RecoveryDownstream: Chromatography, Filtration, Ultrafiltration, Final FillingCentral Service: Buffer/ Media Preparation, Autoclave, Glasswash and cleaning processes, Sampling of raw materials.
Carry out daily tasks as assigned by Lead Biotechnologist or Manufacturing Supervisor
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