Avinash Ingle's Email & Phone Number

💼 Past Experience

Avinash Ingle holds a B.Tech. in Automotive Engineering from IIM-Calicut, and currently works as a Technical Support Engineer at NovartisIndustry of Pharmaceuticals.Avinash Ingle's B.Tech. experience in Automotive Engineering has given him skills in Fermentation, Validation, Microbiology, Sop, GMP, GLP, Technology Transfer, Pharmaceutical Industry, Regulatory Affairs, Equipment Qualification, Biotechnology, Process Simulation, R&D, Cleaning Validation, FDA, Lifesciences,Downstream Processing, Chromatography, GxP, Quality System, Continuous Improvement, Quality by Design, Fermentation Technology, Quality Auditing, Biopharmaceuticals, V&V, Aseptic Processing, 21 CFR Part 11, Vaccines, Monoclonal Antibodies, Sterilization, cGMP manufacturing, Quality Assurance, Lean Manufacturing, FDA GMP, CAPA, Change Control, Purification, Cell Culture, Lyophilization, Filtration, cGMP practices, Quality Control, Biosimilars, Chemistry, Environmental Microbiology, OOS, Laboratory, Cell, Molecular BiologyAvinash Ingle is a Head-Production at Novartis.He has over 10 years of experience in various production and engineering areas such as fermentation, validation, microbiology, Sop, GMP, GLP, Technology Transfer, Pharmaceutical Industry, Regulatory Affairs, Equipment Qualification, Biotechnology, Process Simulation, R&D, Cleaning Validation, FDA, Lifesciences, Downstream Processing, Chromatography, GxP, Quality System, Continuous Improvement, Quality by Design, Fermentation Technology, Quality Auditing, Biopharmaceuticals, V&V, Aseptic Processing, 21 CFR Part 11, Vaccines, Monoclonal Antibodies, Sterilization, cGMP manufacturing, Quality Assurance, Lean Manufacturing, FDA GMP, CAPA, Change Control, Purification, Cell Culture, Lyophilization, Filtration, cGMP practices, Quality Control, Biosimilars, Chemistry, Environmental Microbiology, OOS, Laboratory, Cell, Molecular BiologyAvinash Ingle is currently a Head-Production at Novartis.He has over 10 years of experience in various production and engineering areas such as fermentation, validation, microbiology, Sop, GMP, GLP, Technology Transfer, Pharmaceutical Industry, Regulatory Affairs, Equipment Qualification, Biotechnology, Process Simulation, R&D, Cleaning Validation, FDA, Lifesciences, Downstream Processing, Chromatography, GxP, Quality System, Continuous Improvement, Quality by Design, Fermentation Technology, Quality Auditing, Biopharmaceuticals, V&V, Aseptic Processing, 21 CFR Part 11, Vaccines, Monoclonal Antibodies, Sterilization, cGMP manufacturing, Quality Assurance, Lean Manufacturing, FDA GMP, CAPA, Change Control, Purification, Cell Culture, Lyophilization, Filtration, cGMP practices, Quality Control, Biosimilars, Chemistry, Environmental

🎓 Education

Avinash Ingle has a Masters in Business Administration (MBA) from Indian Cultural and Social Foundations' (ICFAI) in 2014. Avinash Ingle has also a Master of Science in Microbiology from Government Institute of Science,(GIS) from January 1993 to January 1996. Avinash Ingle has also a Post-graduate certificate in Project Management from Indian Cultural and Social Foundations' (ICFAI) in 2014.

💡 Technical & Interpersonal Skills

Avinash Ingle has a long record of innovation, product development leadership, and quality control system improvement. He has been an essential member of the product validation team at Genzyme and Sandoz, responsible for developing and QC'ing product sagas. In his previous work experience, he has excelled at problem solving and working collaboratively with colleagues. Avinash has a clear understanding of how to build a quality system and drive continuous improvement. He is also skilled in quality assurance and product development leadership, having worked on characterizing and inspecting products. stints at contamination-alarm company CMC and as a public health inspector in India.Avinash Ingle is highly educated and has a background in engineering and manufacturing science and technology. He has experience in fermentation, validation,microbiology, sopp, gmp,GLP, technology transfer, pharmaceutical industry, regulatory affairs, equipment qualification, biotechnology, process simulation, r&D, cleaning Validation, FDA, lifesciences, downstream processing, chromatography, gxp, quality system, continuous improvement, quality by design, fermentation technology, quality auditing, biopharmaceuticals, v&v, aseptic processing, 21 CFR part 11, vaccines, monoclonal antibodies, sterilization, cgmp manufacturing, quality assurance, lean manufacturing, fdagmp, capa, change control, purification, cell culture, lyophilization, filteration, cgmp practices, quality control, biosimilars, chemistry, environmental microbiology, oos, laboratory, cell, molecular biology.