Krishnam Raju Shanmukhi Email & Phone Number | As a Manager at Biological E. Limited, a leading pharmaceutical company that develops and manufactures sterile injectables like vials, PFS and device products, I oversee the quality assurance activities for the formulation facility. I have a master's degree in microbiology and over 10 years of experience in the pharmaceutical industry, spanning across quality assurance, manufacturing, and regulatory affairs. My core competencies include IPQA, QMS, process validation, media fill, batch release, regulatory submissions, APQR, audit management, and customer support. I leverage my programming skills and use MES and CPV tools to monitor and improve the manufacturing processes. I am passionate about ensuring the highest standards of quality and compliance for the products that impact the health and well-being of millions of people. I work collaboratively with cross-functional teams and external stakeholders to deliver safe, effective, and timely solutions.

Krishnam Raju Shanmukhi

As a Manager at Biological E. Limited, a leading pharmaceutical company that develops and manufactur...
Hyderabad, Telangana, India

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Krishnam Raju Shanmukhi’s Location Hyderabad, Telangana, India

Krishnam Raju Shanmukhi’s Current Industry Biological E

Krishnam Raju Shanmukhi’s Prior Industry Mylan Laboratories | Aurobindo Pharma | Strides | Gland Pharma

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Senior Manager

2024-07-01 00:00:00 - Present

Manufacturing Team Lead

2015-01-01 00:00:00 - 2018-03-01 00:00:00

Executive

2011-09-01 00:00:00 - 2014-12-01 00:00:00

Executive

2009-11-01 00:00:00 - 2011-08-01 00:00:00

Jr.chemist

2007-03-01 00:00:00 - 2009-10-01 00:00:00

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Krishnam Raju Shanmukhi is a As a Manager at Biological E. Limited, a leading pharmaceutical company that develops and manufactures sterile injectables like vials, PFS and device products, I oversee the quality assurance activities for the formulation facility. I have a master's degree in microbiology and over 10 years of experience in the pharmaceutical industry, spanning across quality assurance, manufacturing, and regulatory affairs. My core competencies include IPQA, QMS, process validation, media fill, batch release, regulatory submissions, APQR, audit management, and customer support. I leverage my programming skills and use MES and CPV tools to monitor and improve the manufacturing processes. I am passionate about ensuring the highest standards of quality and compliance for the products that impact the health and well-being of millions of people. I work collaboratively with cross-functional teams and external stakeholders to deliver safe, effective, and timely solutions.