Mark Krishna

Mark Krishna

Senior Manager, Quality Rp @ Bristol Myers Squibb

About Mark Krishna

Mark Krishna is a Senior Manager, Quality RP at Bristol Myers Squibb in Singapore, with extensive experience in quality assurance and regulatory affairs within the pharmaceutical industry.

Company

Mark Krishna is currently employed at Bristol Myers Squibb as a Senior Manager, Quality RP in Singapore. Bristol Myers Squibb is a global biopharmaceutical company committed to scientific excellence and innovation. The company focuses on developing a range of biopharmaceutical products primarily in oncology, cardiovascular, and immunology. Bristol Myers Squibb supports various patient access programs and collaborates extensively with academic and research organizations globally.

Title

Mark Krishna holds the position of Senior Manager, Quality RP at Bristol Myers Squibb. In this role, he is responsible for ensuring compliance with regulatory standards and implementing quality management systems.

Education and Expertise

Mark Krishna has an extensive educational background that complements his professional experience. He earned a Master of Pharmacy from the University of Szeged, Hungary. He later obtained a Specialist Diploma in Biopharmaceutical Technology from Temasek Polytechnic, Singapore. He also holds a Postgraduate Certificate in Pharmacy Practice from the National University of Singapore and a Postgraduate Certificate in Business Analytics from the Texas McCombs School of Business.

Previous Roles

Before joining Bristol Myers Squibb, Mark Krishna accumulated significant experience in various roles. He worked as a QA Manager at LINK - A Clinigen company from 2020 to 2022. From 2015 to 2020, he served as a Quality Pharmacist at Kuehne+Nagel in Singapore. At NTUC Health Co-operative Limited, he worked as a Pharmacist from 2011 to 2015. His career began as an Operations Technician at GSK Biologicals from 2009 to 2011.

Quality Assurance and Regulatory Affairs Expertise

Mark Krishna has a robust background in quality assurance and regulatory affairs within the pharmaceutical industry. He has extensive experience in implementing quality management systems and ensuring compliance with regulatory standards. His roles have often involved collaboration with cross-functional teams to achieve quality and compliance objectives. Additionally, he has a deep understanding of the pharmaceutical supply chain and its regulatory requirements.

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