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Sachin Maled

Sachin Maled

Senior Manager of Industry Solutions

Sachin Maled is a senior manager of industry solutions at ValGenesis, with more than 12 years of experience. His expertise spans manufacturing, commissioning, qualification, and technical sales across the pharmaceutical and food and beverage industries. Maled specializes in compliance, digital validation, and cleaning validation. In his role, he provides guidance in process and automation design and helps clients navigate complex regulatory requirements. He holds a master's in business administration from the IU International University of Applied Sciences and a bachelor's in biotechnology from North Maharashtra University. 

Blog Posts by Sachin

What Are the Regulatory Expectations for Cleaning Validation?

In the pharmaceutical manufacturing industry, maintaining high standards of cleanliness is not just a best practice but a regulatory necessity. If you’ve ever wondered why cleaning validation is required, the answer is ...

Avoiding Common FDA 483 Observations in Cleaning Validation

In the highly regulated world of pharmaceutical manufacturing, compliance with FDA guidelines is not just a legal requirement, it's a critical component of ensuring patient safety and product efficacy. One area that ...

Best Practices for Impact Assessments in Cleaning Validation

Central to product safety and efficacy is the rigorous process of cleaning validation, which involves assessing and documenting the effectiveness of cleaning procedures to prevent cross-contamination and ensure product ...

Webinars by Sachin

Residual Limits Management as a System, Not a Worksheet

Achieving Regulatory Readiness: How to Minimize Audit Stress

Join our webinar to see how ValGenesis Smart GxP™ helps pharma leaders slash audit prep time by 70%, cut validation cycles by 80%, and reduce observations by 90%—turning compliance into a competitive ...

Challenges and Solutions: A Deep Dive Into Digital CQV

Discover how digital transformation in Commissioning, Qualification, and Validation (CQV) can streamline operations, ensure compliance, and equip you to stay ahead in the evolving pharmaceutical and ...

Common FDA 483 Cleaning Validation Observations and How to Avoid Them

Join our webinar to learn how to overcome the pharmaceutical industry's cleaning validation challenges, avoid FDA Warning Letters, and protect patient safety and product quality.

For OEMs: Drive New Agility in Qualification Service Requests

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Meet Sachin at these Events

April 2026