Harish Dhanashree
Merck KGaA | Global Regulatory Affairs | Oncology | Previously worked with Parexel | Micro Labs
- Role
- Manager Global Regulatory Oncology Strategy at Merck Group
- Location
- Bengaluru, KA, IN
- LinkedIn followers
- 500 followers
About Harish Dhanashree
Dedicated to surpassing professional and personal targets, I am driven by an unwavering commitment to achieving the highest levels of success through the optimal application of my skills. My catalytic management style, coupled with proven communication skills, forms the backbone of my approach, fueled by a genuine passion for fostering positive interpersonal relations.My professional journey is anchored in the dynamic field of Regulatory Affairs, where I seamlessly integrate scientific expertise with a comprehensive understanding of local, regional, and national regulations. Applying analytical and structured problem-solving tools, I navigate complexities with precision, identifying root causes and crafting innovative technical approaches to challenges.In the ever-evolving landscape of global pharmaceutical industries, I thrive on exploring and applying my regulatory expertise. With a rich history in Regulatory Affairs, my experience spans the intricacies of regulatory submissions, adherence to regulatory requirements, and adept utilization of regulatory tools such as eDMS, eRIMS, and Publishing, all of which contribute to the seamless maintenance of product life cycles.I am not just committed to upholding standards; I am driven to set new benchmarks in every endeavor. Join me on this journey of excellence, where my expertise aligns seamlessly with the demands of the pharmaceutical industry, creating a legacy of innovation and regulatory excellence.\"
Experience
Manager Global Regulatory Oncology Strategy
Oct 2024 — Present · Bengaluru, IN
Education
Visveswarapura Institute of Pharmaceutical Science
Master of Pharmacy, Pharmaceutics
2010 — 2012
Soniya Educational Trust College Of Pharmacy
Bachelor of Pharmacy, Pharmacy
2004 — 2008
Skills
- Evmpd
- Regulatory Requirements
- Regulatory Affairs
- Liquent Viewer
- Pharmacovigilance
- Gmp
- Pharmaceutical Industry
- Sop
- Pharmaceutical Development
- First Doc
- Erims (Electronic Regulatory Information Management System)
- Regulatory Submissions
- Formulation Development
- Pharmaceutics
- Cmc
- Veeva Vault
- Pharmacy
- Ectd
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