07/2005 – 04/2007
abgeschlossen
Chemie
, Indien
Chemistry
- Dokument_Studium_011.pdf
06/2002 – 03/2005
abgeschlossen
Chemie
, Indien
Chemistry/ Maths and Physics
- Dokument_Studium_021.pdf
Fotos sind nur für registrierte Arbeitgeber sichtbar
Hier registrieren
Industriemeister/in - PharmazieIndien |
9 Jahre Erfahrung |
Geburtsdatum:
Staatsangehörigkeit:
indisch
32037667
07/2005 – 04/2007
abgeschlossen
Chemistry
06/2002 – 03/2005
abgeschlossen
Chemistry/ Maths and Physics
11/2013 – Bis heute
• Responsible for analytical method development for Related Substances, Assay, Dissolution
Dissolution profile in different media, and Residue analysis for drug products (Tablets/
Capsules) by HPLC / UPLC / UV- Visible spectrophotometer.
• Preparation and review of Development reports, Validation protocols, Validation reports
and conducting validations for products intended for Generic market.
• Reviewing STP’s, Specifications and Sop’s for analytical department related products and
instruments. Preparation and review of the stability compilation data during product development.
• Actively participating in product development strategies ensuring the timely completion of
projects.
• Literature survey for project, guidelines and updating the current developments in
analytical field.
• Responsible to Global Analytical method transfer, coordinating with Quality control team to resolve the technical related issues
• Trouble shooting of Analytical Instruments and Methods.
• Effectively involved in the analytical queries from regulatory authorities
• Training the analyst to complete the analyst qualification and on job training in various
analytical techniques.
• Addressing the internal audit conducted by the QA Department.
• Ensure to perform preventive maintenance and calibration of analytical instruments as per
Schedule
• Indenting Chemicals, Columns, Reference standards and Impurity standards and follow up.
• Ensuring Lab safety.
Weitere Profildaten werden sichtbar, wenn Sie sich registrieren
Zur Registrierung11/2011 – 11/2013
• Preparation and review of Development reports, Validation protocols, Validation reports
and conducting development and validations for products intended for Generic market.
• Actively participating in product development strategies ensuring the timely completion of
projects.
• Exploring latest analytical developments in the pharmaceutical industry.
• Trouble shooting of Analytical Instruments and Methods.
• Effectively involved in the analytical queries from regulatory authorities.
• Responsible to Global Analytical method transfer.
• Responsible for developing methods for estimation of ions and polar compounds by ion
chromatography.
• Ensuring the Lab safety
02/2010 – 04/2011
• HPLC method development & method validation for drug products. Conducting the stability studies.
• Pharmaceutical products including stability studies.
• Identification of unknown impurities by using analytical techniques.
• Preparation and review of development reports, validation protocols, summary reports and test procedures.
• Active participant in analytical method transfer and analytical complaints.
10/2007 – 11/2009
• HPLC method validation for active pharmaceutical ingredients.
• Preparation of COA’s for raw material and finished product.
• In-process and finished product analysis.
• Preparation and certification of in-house working standards.
• Calibration of Instruments like HPLC, UV-Visible Spectrophotometer, Dissolution tester
• Performing the comparative dissolution profiles of generic drug product Vs. Innovator product with dissolution profiles in different media (DPDM).
–
–
• Responsible for analytical method development for Related Substances, Assay, Dissolution
Dissolution profile in different media, and Residue analysis for drug products (Tablets/
Capsules) by HPLC / UPLC / UV- Visible spectrophotometer.
• Preparation and review of Development reports, Validation protocols, Validation reports
and conducting validations for products intended for Generic market.
• Reviewing STP’s, Specifications and Sop’s for analytical department related products and
instruments. Preparation and review of the stability compilation data during product development.
• Actively participating in product development strategies ensuring the timely completion of
projects.
• Literature survey for project, guidelines and updating the current developments in
analytical field.
• Responsible to Global Analytical method transfer, coordinating with Quality control team to resolve the technical related issues
• Trouble shooting of Analytical Instruments and Methods.
• Effectively involved in the analytical queries from regulatory authorities
• Training the analyst to complete the analyst qualification and on job training in various
analytical techniques.
• Addressing the internal audit conducted by the QA Department.
• Ensure to perform preventive maintenance and calibration of analytical instruments as per
Schedule
• Indenting Chemicals, Columns, Reference standards and Impurity standards and follow up.
• Ensuring Lab safety.