Saurabh Joshi is renown for his contributions in executing robotics and automation projects for industry 4.0 transformation. He has been a keynote speaker and trainer in various life sciences forums and conferences, globally.
An industry professional with over 20 years hands on experience in Quality operations, Quality systems, Tech. transfer, Compliance, Validation and Qualifications; has successfully lead numerous regulatory inspections from USFDA, MHRA, WHO GMP (Geneva), HPRA for reputed organizations he has been a part of, such as, Cipla, Microlabs, Wockhardt, Sun Pharma to name a few. He has been an external Quality consultant with Merck specialties Pvt. Ltd. (A Merck KGaA, Darmstadt Germany company) guiding from shop floor at site to leading corporate level functions.
His consulting expertise includes, gap assessments and SOP preparation, regulatory inspections, QMS, technology transfer, Process Validation and equipment qualification, GMP, Data Integrity and Artificial Intelligence & Robotics.
He’s currently working with ValGenesis as Director-Industry solution. In his role he’s responsible for expanding customer outreach and demonstrate platform capabilities with ValGenesis’ solutions to life science companies.
This latest webinar will showcase possibilities with some case study examples of what can be done. The case study for manufacturing, maintenance, instrumentation, Quality assurance and regulatory assurance functions will be discussed. It is a must attend webinar to...
Technology transfer in pharmaceuticals seems complex or simple based on who is looking at it. For site manufacturing team, it may be complex as they’ve to do go through a series of processes before they can term a transfer...
Equipment qualification and process validation is a cumbersome activity if realistic but compliant approach is not applied. This session should help responsible personnel and teams to apply efforts in right direction to ensure regulator satisfaction at the same time...