Vinod Kumar Email & Phone Number

Jammu & Kashmir, India

• Analytical method development, validation and transfer of method for pharmaceutical dosage forms (like oral solid, oral liquid) as per the regulatory requirements.
• Analytical method development and validation for pharmaceutical dosage forms.
• Literature search related to the drug substance, create analytical profiles.
• Execution of analytical method transfer for pharmaceutical dosage forms.
• Analysis of routine samples (product development batches, stability study samples… Show more
• Analysis of routine samples (product development batches, stability study samples, raw materials etc.).

Panchkula, Haryana, India

• Analytical method validation, transfer and verification as per market.
• Analytical method validation report preparation and methods transfer to production site.
• Protocol based studies execution, data compilation and review of analytical data.
• Regulatory Markets compliances. Handling of Incidence and change control.
• Trouble shooting and problem solving of instrument and analytical methods.
• API and excipient analysis.

Noida, Uttar Pradesh, India

• Analytical method validation of OSD formulation.
• Problem solving of various analytical methods and instruments.
• Execution and maintains of analytical data archival.
• Daily and Monthly Instrument Calibration Balance, PH Meter, HPLC.
• Routine sample analysis F&D Sample

Solan, Himachal Pradesh, India

• Analytical method validation of injectable formulation, Lyophilized Product.
• Active participation in SOP preparation and updation.
• Calibration and maintains of various analytical instrument and equipment. And maintains of analytical data archival.
• Analytical method validation by GC.
• Analytical method Verification and transfer as per Customer and market.
• Analytical Cleaning validation

Vadodara, Gujarat, India

• Analytical Method development and validation of Complex injectable formulation,peptides,Nano-suspension
• Qualification and reports preparation for Impurity profiles.
• Daily and monthly calibration of instrument.
• Maintain and follow GLP procedure.

Solan, Himachal Pradesh, India

• Routine analysis of finished products formulation F&D sample of Parental dosage forms.
• Method Validation of new Product
• Compliance of product and analytical data as per GLP guidelines.
• Perform all works using appropriate safety majors and follow the chemical hygiene plan

Master'S Degree, Pharmacology, A

Bachelor'S Degree, Pharmacy

12, Biology, General, 2Nd Division