Experience

Encube Ethicals Private Limited

• India
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• Officer

  • Sep 2019 - Present

  • Formulation and Development 1. Formulation Development of semisolid dosage forms for US and Europe Market. 2. Formulation Development of oral semisolid dosage forms_ ANDA 3. Method development and Method Transfer. 4. Carrying out Literature Survey, Preformulation Studies, Compatibility Studies Feasibility Studies, Developmental Trials and Stability study as per requirement. 5. Manufacturing of Optimization, scale up batches and participating in exhibit batches with TT personnel at plant. 6. Documentation activities of project: preparing Compatibility Study Protocol, Stability Study Protocol, Filling of Lab Notebook, compilation of data of batches. 7. Destruction/ Reconciliation of controlled drug substances. 8. Maintain GMP and Safety procedure in laboratory. 9. Update the project status on daily basis to the immediate superior. Show less



PERRIGO LABORATORIES INDIA PRIVATE LIMITED

• India
• Mining
• 1 - 100 Employee

• Research Assistant

  • Sep 2018 - Sep 2019

  • Formulation and Development 1. Formulation Development of oral solid dosage forms for US and Europe Market. 2. Formulation Development of oral solid dosage forms_NDA 3. Formulation Development of topical dosage forms_ ANDA 4. Carrying out Literature Survey, Preformulation Studies, Compatibility Studies Feasibility Studies, Developmental Trials and Stability study as per requirement. 5. Manufacturing of Optimization, scale up batches and participating in exhibit batches with TT personnel at plant. 6. Documentation activities of project: preparing Compatibility Study Protocol, Stability Study Protocol, Filling of Lab Notebook, compilation of data of batches. 7. Destruction/ Reconciliation of controlled drug substances. 8. Maintain GMP and Safety procedure in laboratory. 9. Update the project status on daily basis to the immediate superior. Show less



pharmaceutical

• Navi Mumbai

• Trainee

  • Sep 2017 - Sep 2018

  1. Preparation of SOP, BMR, BPR and APQR,Training Record 2. Review of BMR, BPR, Artwork 3. Issuance of SOP, BMR, BPR, Protocol 4. Archival and Retrieval of SOP, BMR, BPR, APQR, Protocols, Training Records, Cleaning, Validation, Qualification, Deviation, Change Control, Market compliant, Site Master file etc. 5. Maintaining the retention samples. 1. Preparation of SOP, BMR, BPR and APQR,Training Record 2. Review of BMR, BPR, Artwork 3. Issuance of SOP, BMR, BPR, Protocol 4. Archival and Retrieval of SOP, BMR, BPR, APQR, Protocols, Training Records, Cleaning, Validation, Qualification, Deviation, Change Control, Market compliant, Site Master file etc. 5. Maintaining the retention samples.