Scientist in Drug Product Attributes

4 days ago


Bachupally Hyderabad Telangana, India Dr. Reddy's Laboratories, Inc. Full time

**Key Responsibilities**:

- Knowledge on Method development and method qualification on Excipients for Biosimilars
- Execution of method transfer/ method validation between QC and ASAT for New and Tech transfer products.
- Execution of validations as per Protocol and complies to current SOP requirements.
- Expert in data analysis for HPLC and IC and Writing reports
- Review of analytical method development reports before initiation of method validation study and understand the criticality of each method.
- Ensuring all pre requisites before initiation of method validation, transfer activities.
- Preparation of Analytical method transfer protocols as per need.
- Ensuring Safety practices at work place.
- Maintenance of laboratory as per the cGLP.
- Having the good documentation skill
- Getting trained for all the instruments and SOPs on time.

**Education & Experience**:

- Master in Science with 7 + years of experience in Analytical Method development, qualifications of Excipients.
- Having knowledge on analytical methods validation instrumentation and calibrations
- Well versed with analytical instrumentation like HPLC, IC etc.
- Should have good knowledge of cGMP and cGLP

Skills Required: Well versed with analytical instrumentation like HPLC, IC etc.


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