
Pharmaceutical Process/Cleaning Validation SME
3 days ago
IMPORTANT NOTE: Candidate should have prior work experience in Pharmaceutical Industry in QA role in Validation. Do NOT apply if you have software testing experience
Company DescriptionQuascenta specializes in offering comprehensive validation lifecycle management software solutions to empower pharmaceutical manufacturing sites. Our flagship products, e
Residue Pro, e
Process Pro, ValDoc Pro, QMS Pro and e
Log Pro, are designed to streamline QMS, product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. We provide innovative solutions tailored to meet unique requirements, with experienced Subject Matter Experts (SMEs) analyzing data and recommending improvements. Role DescriptionThis is a full-time on-site role.
The candidate will be responsible for providing technical support to companies on the following software products:ValDoc Pro - Qualification lifecycle management softwaree
Log Pro - Electronic logbookQMS Pro - Quality Management system software
You will also be responsible for the following:Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online
Write test scripts and execute them. Open bug tickets where required.QualificationsPrior experience using a QMS software
Experience in qualification of equipment/instruments
Experience in process validation a plus
Fluency in Hindi a must.
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