Research Associate in ADL Department for AMD/ AMV/ AMT/ Stability/ GLP

Job Posted on Aug 6, 2022

Recruiter Type:Consultancy
Consultancy Name:MoonStar Consultancy
Hiring For:Pharma Company
Contact Person:Sujeet
Required in:Formulation
Job Department(s):Research, ADL
Job Title:Research Associate in ADL Department for AMD/ AMV/ AMT/ Stability/ GLP
Qualification:MSc / B-Pharma/ M-Pharma
Job Details:

Department: AMD/AMT/ AMV
Qualification: M.Sc / B.Pharma/ M.Pharma
Designation : Junior/ Senior Research Associate 
Experience: 2-8 Years
Vacancy: 9

Department: Stability (HPLC)
Qualification: M.Sc / B.Pharma/ M.Pharma
Designation : Junior / Senior Research Associate
Experience: 2-8 Years
Vacancy: 7

Department: DQA/GLP/NR Team
Qualification: M.Sc / B.Pharma/ M.Pharma
Experience: 2-6 Years
Vacancy: 5
Regulatory Exposure:Not Required
Experience:2-8 Years
Last Date:10/08/2022
Additional Details:Job Description:
1.Analytical method developments for Assay/CU/BU/Dissolution & RS with AMD Reports.
2. Responsible for preparation of Specification/STP/MoA/ Protocols & Report.
3. Forced degradation study with documentation like protocols & Reports
4. Excipients compatibility study with documentation like protocols & Reports
5. Stress study, Photo stability, Breakability study and documentation
6. Daily troubleshooting of day to day activity, personal involvement with analyst.
7. Deficiency study & Respond.
8. Pre-formulation study documentation like protocols & Reports
9. Impurity Profiling of Drug substance & Drug products.
10. Testing Method evaluation, comparison and compilation and implementation.
11. Routine analysis of R&D sample Assay/CU/BU/Related substances and report with
12. Maintenance of Working standard/impurity/Reference standard itc
13. Calibration of instruments like HPLC/UV Spectrophotometer/HPLC etc.
14. Analytical method transfer of Assay/CU/BU/Dissolution & RS with AMD Reports
15. Evaluation of documents like Specification, STP/ MoA, Monographs as per IP/BP/USP etc.

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