
Pharmaceutical Qualification SME
2 days ago
Company DescriptionAt Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles.
With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role DescriptionThis is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. 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.QualificationsBPharm or Biotechnology degree
Will be expected to serve minimum 2 years with the company if offered a position.
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India Quascenta Full time ₹ 9,00,000 - ₹ 12,00,000 per yearIMPORTANT 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...
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