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Experienced scientist dedicated to excelling in the design and development of pharmaceutical products, emphasizing the enhancement of patient well-being. Expertise in pre-formulation studies, formulation technology, and process development leverages advanced methodologies to improve bioavailability for poorly soluble compounds across diverse dosage forms, including modified release, targeted delivery, and sterile preparations. Proven leadership skills include guiding teams, managing complex projects, and achieving strategic objectives through effective planning, mentorship, and cross-functional collaboration. Recognized for a collaborative approach and unwavering commitment to excellence, offering a fresh perspective and strong dedication to quality and success while aspiring to contribute as a scientific leader and subject matter expert in comprehensive development and manufacturing strategies.

More than Twenty nine years of experience in Formulation development from well-esteemed organizations and having exposure to Generic product development for Global markets, Novel drug delivery system, Quality by design, Analytical development, Technology Transfer, NCE product development, Intellectual property rights (IPR) and Regulatory affairs. Currently working as Senior Vice President – Head Formulation development (Orals, Injectables, Ophthalmics and TT-IL/OL) in Glenmark Pharmaceuticals Ltd, Mumbai, Maharashtra, India.

Detail-oriented M.Pharm graduate specializing in formulation development, analytical instrumentation, and stability studies per ICH guidelines. Experienced in Quality Control (QC), Quality Assurance (QA), and pharmaceutical research, with hands-on laboratory techniques and in-vitro evaluation. Committed to maintaining accurate documentation and ensuring compliance with industry standards.

M.Pharm (Pharmaceutics) postgraduate with hands-on experience in Formulation and Development of tablet dosage forms and over two years of teaching experience in pharmacy education. Skilled in wet granulation, pre-formulation studies, and tablet evaluation tests, with strong exposure to cGMP, SOP, and BMR documentation. Experienced in delivering theory and practical sessions, mentoring students, and maintaining laboratory standards. Detail-oriented professional with strong technical documentation, communication, and coordination skills, seeking opportunities in pharma industry or academia.

SURYAA ANISH S.R.

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M.S. - Pharmaceutics (Industrial Pharmacy)

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M.S. - Pharmaceutics (Industrial Pharmacy)

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