We are dealing with customized value added various certification courses under Training and Placement program for fresheners looking to introduce themselves in reputed pharmaceutical industries as well as experience persons which are interested for smart move.
We have designed our programs against guidance of reputed pharmaceutical industries across India. Advance digital theoretical trainings from industry experts, professional soft skill enhancement workshops, working /Laboratory skill developments against current trends, Mock interviews as per industry protocols, launching in reputed industries are some of our key performance indicators.
Our journey started from Jan 2017 at Satara city of Maharashtra. Within two years , students from 213 + colleges across India attached with us and we are succeeded to recruit around 620 students in reputed pharmaceutical companies across India.
Provides Pharmaceutical Technical Trainings /Workshops to Employees related to Quality Control/ Quality Assurance / Microbiology at factory location based on requirement for Topics Like GMP, GLP, GDP, Data Integrity , 21 CFR Part 11, Stability Studies, Process Validation, Cleaning Validation, Method Validation, Quality Management Systems, Qualifications etc. Also provides skill set development and troubleshooting trainings on laboratory operations at factory locations.
Provides Pharmaceutical Technical Support for activities like Qualifications ( Instrument / Equipment / Area / Operating Software’s) , Validations ( Water Generation System/ Process/ Methods/ HVAC/ Boilers etc). SOP for all departments, QMS Documentation , OOS/OOT/ Deviations Investigations as per Regulatory Authorities requirements.
Provides Analytical supports for Research and Development on Educational or Industrial Projects By using sophisticated Instrumentation like HPLC, UV, IR, Dissolution, Polarimeters, Karl fisher etc Also provides Method Development / Validation / Method Updation on HPLC/ UV.
Purchase Old Pharmaceutical Instruments / Equipments and resale after refurbishment with assured maintenance like HPLC/ UV/ Dissolution / Analytical Balances.
22 years as Key functional of Quality Control, Quality Assurance, Method Development, Validations, Documentation and QMS in various Multinational pharmaceutical Industries (API Manufacturing, Sterile and Non- Sterile Formulations).
Worked in regulatory environment of USFDA , TGA , MHRA, MCC, HEALTH CANADA(CANADA), ANVISA (Brazil) , EMEA (European Union), SFDA, WHO etc.