Shivangi Sharma

am a highly skilled pharmaceutical professional with expertise in Good Manufacturing Practice (GMP), aseptic production, quality assurance, and regulatory compliance. With a strong background in pharmaceutical sciences and a Masters in Biotechnology, I have gained extensive experience in gene therapy manufacturing, biologics production, and batch release processes. My career has spanned roles at Charles River Laboratories and Titan Biotech, where I have successfully managed complex pharmaceutical operations, ensured compliance with industry standards, and driven continuous improvement initiatives.

I have hands-on experience as a Releasing Officer, overseeing the release of batches for medicinal products, and I am well-versed in conducting root cause analysis and implementing corrective actions to resolve quality issues. I am committed to maintaining high-quality standards, optimizing operational efficiency, and contributing to the advancement of the pharmaceutical industry.

Known for my strong communication and problem-solving skills, I thrive in collaborative environments and have successfully led cross-functional teams to deliver critical projects. I am passionate about using my expertise to ensure the highest level of product quality and patient safety, and I am always eager to take on new challenges in the ever-evolving field of pharmaceuticals.

Biotech Microbiology

MSC in Biotechnology