Pharmaceutical Process/Cleaning Validation Software Specialist Quascenta

3.0 - 7.0 years

0 Lacs

chennai, tamil nadu

On-site

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 upl...

Posted 2 months ago

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Sr. Executive Syngene International Limited

3.0 - 7.0 years

0 Lacs

karnataka

On-site

You will be responsible for ensuring safety as a top priority at Syngene. Compliance with safety guidelines, procedures, and SOPs is essential to maintain a safe work environment. - Adhere to Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for a safe work environment. - Complete assigned trainings in a timely manner and comply with training procedures. - Participate in mandatory trainings related to data integrity, health, and safety. - Maintain compliance with Good Manufacturing Practices and Good Documentation Practices. - Follow Standard Operating Procedures and Operational Control Procedures. - Support training programs on procedures, protocols, and on-the-j...

Posted 3 months ago

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Jr. Executive Syngene International Limited

1.0 - 5.0 years

0 Lacs

karnataka

On-site

As a Jr. Executive at Syngene International Ltd., you will be responsible for maintaining good aseptic behavior inside the Biologics operations facility and performing various downstream activities such as Assembly preparation, Dispensing of raw materials, Buffer Preparation, Harvest Clarification, Chromatography operation, and more. You will operate and clean downstream equipment according to standard operating procedures, monitor and control specific operations, maintain quality records, and perform in-process product sampling and storage. Additionally, you will be required to prepare and review operation-related documents, take ownership of the assigned DSP area and equipment/instrument r...

Posted 5 months ago

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