Pharmaceutical equipment qualification SME

As a QA Validation Specialist at Quascenta, you will play a crucial role in providing technical support for software products such as ValDoc Pro, eLog Pro, and QMS Pro. Your responsibilities will include: - Assisting companies with uploading SOPs and managing qualification in the application - Executing qualification scripts (IQ/OQ/PQ) online - Writing and executing test scripts - Opening bug tickets when necessary Qualifications required for this role: - Prior experience in using QMS software - Experience in equipment/instruments qualification - Experience in process validation will be an added advantage - Fluency in Hindi is a mandatory requirement Quascenta is a leader in offering validation lifecycle management software solutions for pharmaceutical manufacturing sites. Our products such as eResidue Pro, eProcess Pro, ValDoc Pro, QMS Pro, and eLog Pro are designed to enhance QMS, product manufacturing, and cleaning processes, ensuring compliance, efficiency, and cost savings. We are committed to providing innovative solutions tailored to meet unique requirements, supported by experienced Subject Matter Experts (SMEs) who analyze data and suggest improvements.,