Iam Nousheen working as faculty in kamineni groups ..i have 4 years of experience in teaching in microbiology for MBBS, BDS and para-medical and Nursing...Am good at teaching all topics of microbiology & well trained in mycology and virology...
Iam Nousheen working as faculty in kamineni groups ..i have 4 years of experience in teaching in microbiology for MBBS, BDS and para-medical and Nursing...Am good at teaching all topics of microbiology & well trained in mycology and virology...
I can teach MSc and BSc students. Subjects - Microbiology biotechnology
I can teach MSc and BSc students. Subjects - Microbiology biotechnology
Nanotechnologist/Entrepreneur with 12 Years of experience in the field of Business and Management consulting in about three countries including UK, India and Australia and have enough skills in TRAINING and TEACHING
Nanotechnologist/Entrepreneur with 12 Years of experience in the field of Business and Management consulting in about three countries including UK, India and Australia and have enough skills in TRAINING and TEACHING
I m a teacher and I m taking Tution’s at my place and online Tution’s too. My qualifications are M.sc microbiology, MA English and B.Ed with 4 years of experience. I can take classes in biology science classes from inter to degree
I m a teacher and I m taking Tution’s at my place and online Tution’s too. My qualifications are M.sc microbiology, MA English and B.Ed with 4 years of experience. I can take classes in biology science classes from inter to degree
Iam kanakanti.saritha, i have completed MSC MICROBIOLOGY, M.ED . Iam having 10 yrs experience in teaching microbiology for bsc nursing ,bsc mlt, dmlt,mlt students.iam having passion of teaching .from last 6 months iam having experience in online teaching to students.
Iam kanakanti.saritha, i have completed MSC MICROBIOLOGY, M.ED . Iam having 10 yrs experience in teaching microbiology for bsc nursing ,bsc mlt, dmlt,mlt students.iam having passion of teaching .from last 6 months iam having experience in online teaching to students.
I am a Quality Assurance/Quality Control Professional with 14+ years of experience in Healthcare, Pharmaceutical, Clinical research and Medical Device, Software industries with exposure to 10+ regulatory inspections from FDA, EMA, ANVISA, TGA, DCGI, CAP and NABL and 180+ audits, from Sponsor, Pharmacovigilance, Internal, External, Third party and corporate audits with compliance to ISO 9001:2008, 15189:2008, 13485:2003 and 17025, GxP, 21 CFR part 11, ISMS (ISO 27001), HIPAA compliance and various regulatory guidelines. Expertise in Quality System development to comply with relevant medical device regulations specifically ISO 13485:2003, FDA 21 CFR Section 820 & EC Medical Device Directive 93/42/EEC, Experience in validation of bio-analytical instruments and usage of LIMS, LDMS, Oracle Clinical, Argus and MedDRA software, Expertise in implementation of Quality Management System by implementing document and Change control, deviation management, Excellent knowledge about validation procedures, preparation and review of Protocols, ICD, IB, CRS and SOPs Completed External Auditor course from (CAP) Collage of American Pathologist, USA. Can work and supervise in all areas of Clinical Research industry and CAP & NABL accredited diagnostic laboratories. Proven leadership skills involving, managing, developing and motivating teams to achieve their objectives, dedicated to maintaining high quality standards. Able to work on own initiative and as part of a team.
I am a Quality Assurance/Quality Control Professional with 14+ years of experience in Healthcare, Pharmaceutical, Clinical research and Medical Device, Software industries with exposure to 10+ regulatory inspections from FDA, EMA, ANVISA, TGA, DCGI, CAP and NABL and 180+ audits, from Sponsor, Pharmacovigilance, Internal, External, Third party and corporate audits with compliance to ISO 9001:2008, 15189:2008, 13485:2003 and 17025, GxP, 21 CFR part 11, ISMS (ISO 27001), HIPAA compliance and various regulatory guidelines. Expertise in Quality System development to comply with relevant medical device regulations specifically ISO 13485:2003, FDA 21 CFR Section 820 & EC Medical Device Directive 93/42/EEC, Experience in validation of bio-analytical instruments and usage of LIMS, LDMS, Oracle Clinical, Argus and MedDRA software, Expertise in implementation of Quality Management System by implementing document and Change control, deviation management, Excellent knowledge about validation procedures, preparation and review of Protocols, ICD, IB, CRS and SOPs Completed External Auditor course from (CAP) Collage of American Pathologist, USA. Can work and supervise in all areas of Clinical Research industry and CAP & NABL accredited diagnostic laboratories. Proven leadership skills involving, managing, developing and motivating teams to achieve their objectives, dedicated to maintaining high quality standards. Able to work on own initiative and as part of a team.
I am presently undergoing my research in the feild of VLSI. I feel more interest in teaching any one by which I can share my knowledge to every one. I am very clear about the subject and can teach anyone with high patience and care.
I am presently undergoing my research in the feild of VLSI. I feel more interest in teaching any one by which I can share my knowledge to every one. I am very clear about the subject and can teach anyone with high patience and care.
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