Anantnag Dharmapuri Email & Phone Number | I have been working as a Quality Assurance Asst. Manager at Ipca Laboratories Limited since February 2021, after gaining over 17 years of experience in quality assurance and quality control in the pharmaceutical industry. Ipca Labs is a leading manufacturer and exporter of APIs and formulations, and my mission is to ensure quality, compliance, and safety of the products and processes. In my current role, I review, assess, and close CCP and TCCP, coordinate with concerned persons, update the SCM system, and lead the CCRB meet fortnightly. I also review risk assessments, quality trends, SOPs, QMS documents, and provide training on quality systems. I have implemented and reviewed various software systems for document management, training, and 21 CFR Part 11 compliance. I have a strong expertise in GLP, SOP, and quality system management, and I am skilled in analytical and problem-solving techniques. I am passionate about delivering quality and excellence, and I am always eager to learn and grow in my field.

Anantnag Dharmapuri

I have been working as a Quality Assurance Asst. Manager at Ipca Laboratories Limited since February...
Bengaluru, Bengaluru, India

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Anantnag Dharmapuri’s Email anantnag.dharmapuri@ipca.com

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Anantnag Dharmapuri’s Location Bengaluru, Bengaluru, India

Anantnag Dharmapuri’s Current Industry Ipca Laboratories

Anantnag Dharmapuri’s Prior Industry Micro Labs | Cipla | Choksi Laboratories | Alpa Laboratories

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Anantnag Dharmapuri is a I have been working as a Quality Assurance Asst. Manager at Ipca Laboratories Limited since February 2021, after gaining over 17 years of experience in quality assurance and quality control in the pharmaceutical industry. Ipca Labs is a leading manufacturer and exporter of APIs and formulations, and my mission is to ensure quality, compliance, and safety of the products and processes. In my current role, I review, assess, and close CCP and TCCP, coordinate with concerned persons, update the SCM system, and lead the CCRB meet fortnightly. I also review risk assessments, quality trends, SOPs, QMS documents, and provide training on quality systems. I have implemented and reviewed various software systems for document management, training, and 21 CFR Part 11 compliance. I have a strong expertise in GLP, SOP, and quality system management, and I am skilled in analytical and problem-solving techniques. I am passionate about delivering quality and excellence, and I am always eager to learn and grow in my field.