Industriemeister/in - Pharmazie

Indien

9 Jahre Erfahrung

Geburtsdatum:

Staatsangehörigkeit:
indisch

32037667

Hochschulstudium

Zeitraum
Abschluss / Fachbereich / Hochschule
Schwerpunkte

07/200504/2007

abgeschlossen

Master of Science with
Chemie

, Indien

Chemistry

  • Dokument_Studium_011.pdf

06/200203/2005

abgeschlossen

Bachelor of Science (BSc)
Chemie

, Indien

Chemistry/ Maths and Physics

  • Dokument_Studium_021.pdf

Berufserfahrung

Zeitraum
Tätigkeit / Unternehmen
Aufgaben

11/2013Bis heute

Scientist- Analytical Research and Development

, Indien

• 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.

  • Dokument_Praxis_011.pdf

11/201111/2013

Exceutive- Method development Lab

, Indien

• 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

02/201004/2011

Officer-Analytical Research and Development

, Indien

• 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.

10/200711/2009

Analytical Scientist

, Indien

• 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).

Sprachkenntnisse

Sprache
Level
Prüfung / Zertifikat
Deutsch
Grundkenntnisse (A1)

Englisch
Gute Grundkenntnisse (A2)

Weitere Fähigkeiten

Kompetenzen
Führerscheine
Interessen, Hobbys, Persönliches

• 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.

  • Kraftrad

So geht's