Binod Kumar Das Email & Phone Number

Chandigarh, India

Hyderabad, Telangana, India

Responsible for Analytical R & D for Hyderabad and Chandigarh research centre. Heading a highly skilled and enthusiastic team members of more than 80 scientists responsible for API, Vaccine ingredients, CDMO products development and scale up activities.

Chandigarh, India

Heading analytical research and development lab.Responsible for all Analytical research and development activities.

Vadodara, Gujarat, India

Vadodara, Gujarat, India

Responsible for all ADL related activities including Method development, Method Validation, Process support and DQA.Heading a team of about 35 analytical scientists.

Andheri Mumbai

• Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of more than 15 analytical scientists. • Work planning and guidance to for day to day activity. • Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• To Train the new comer to achieve… Show more • Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of more than 15 analytical scientists. • Work planning and guidance to for day to day activity. • Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• To Train the new comer to achieve organizational goal. Show less

Vadodara Area, India

• Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of 10-15 analytical scientists. • Work planning and guidance to for day to day activity. • Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• To Train the new comer to achieve… Show more • Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of 10-15 analytical scientists. • Work planning and guidance to for day to day activity. • Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• To Train the new comer to achieve organizational goal. Show less

Chandigarh Area, India

• Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of 8-10 analytical scientists. • Work planning and guidance to for day to day activity.• Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• Method transfer for routine analysis to… Show more • Method Development for raw material , in-process, intermediates and new active pharmaceutical ingredient by different analytical technique. • Leading a team of 8-10 analytical scientists. • Work planning and guidance to for day to day activity.• Method development for genotoxic impurity.• Responsible for ensuring that all activities carried out in the laboratory is in Compliance with SOP’s and GLP.• Method transfer for routine analysis to location QC.• To work and reply for DMF deficiency.• To Train the new comer to achieve organizational goal. Show less

Ratlam Area, India

1) Method development and method validation activity by HPLC , GC, GC-HS etc..2) Method transfer for routine analysis to location QC.3) To train the new comer to meet organizational goal.4) To carry out stability study for R & D product.5) To help for the work of DMF difficiency.6) Impurity separation by Flash chromatography.7) Method development for the new process development in the laboratory by different analytical technique.

Daman

1) Analysis of raw material as per their specification.2) Analysis of in-process and finish goods such as tablets , capsules , liquid as per specification.3) To carry out stability study of different dosage units.4) To carry out dissolution , disintegration , friability , hardness of solid dosage unit.