Pharmaceutical Process/Cleaning Validation Software Specialist

As an individual with prior work experience in the Pharmaceutical Industry in a QA role, you are ideally suited for the following role at Quascenta: Role Overview: You will be providing technical support on software products such as ValDoc Pro, eLog Pro, and QMS Pro to companies within the pharmaceutical manufacturing sector. Your primary responsibilities will include: - Assisting customers with SOP uploads - Managing qualifications in the application - Executing qualification scripts (IQ/OQ/PQ) online - Writing and executing test scripts - Opening bug tickets when necessary Key Responsibilities: - Provide technical support on ValDoc Pro, eLog Pro, and QMS Pro - Assist customers with SOP uploads and qualification management - Execute qualification scripts online (IQ/OQ/PQ) - Write and execute test scripts - Open bug tickets as needed Qualifications Required: - Prior experience using QMS software - Experience in equipment/instrument qualification - Experience in process validation is a plus - Fluency in Hindi is a requirement In addition to the role requirements, Quascenta specializes in offering validation lifecycle management software solutions tailored for pharmaceutical manufacturing sites. Their products, including eResidue Pro, eProcess Pro, ValDoc Pro, QMS Pro, and eLog Pro, aim to streamline QMS, product manufacturing, and cleaning processes to ensure compliance, efficiency, and cost savings. The company provides innovative solutions customized to meet unique requirements, with experienced Subject Matter Experts (SMEs) analyzing data and recommending improvements.,