Amneal Pharmaceuticals, is an integrated specialty pharmaceutical company powered by a robust U.S. generics business and a growing branded business. Together, our team is working to build one of the most dynamic pharmaceutical companies in our rapidly changing industry. Todays healthcare environment requires a new approach and new ideas. While staying true to our reputation for quality, service and value, we are reinventing our processes, our playbook and our creative partnerships. We are focused on delivering outcomes that meet important medical needs, make quality medicines more accessible and more affordable, and provide solutions for tomorrow’s health challenges. Our leadership and global colleagues are deeply experienced and forward-thinking. We have the capabilities, scale and resources for growth and success. We are nimble and determined. We are Amneal and We make healthy possible.
We are looking for competent, dynamic and motivated candidates for suitable positions for ARD operation at Matoda Plant.
1. Analytical Method Development
Qualification : M.Sc/M.Pharm/PhD
Experience : 2 -5 years
Designation : Executive/ Senior Executive
Job Description:
- Responsible for Analytical method development of Assay, Related compound and dissolution for In-process and Finished product sample.
- Strong and scientific knowledge of areas like Impurity profiling and Forced degradation study.
- Ability to analyze API, Finish product and development stability sample.
- Analytical method validation of Assay, RC and Dissolution test.
- Operation of analytical instruments likes HPLC, IR, KF and Dissolution.
- Analytical data review for development and validation data.
- Should be aware of basic concepts of QbD
- Literature search and DMF review.
2. Analytical Method Validation
Qualification : M.Sc / M.Pharm
Experience : 2-5 years
Designation : Executive/ Senior Executive
Job Description:
- Analytical method validation for the test of RC, Assay , Cleaning, Dissolution, PS, Identification etc.
- Ability to analyze API, Finish product samples.
- Analytical method validation of Assay, RC and Dissolution test.
- Should be aware of basic concepts of protocol preparation and report preparation.
- Operation of analytical instruments likes HPLC, IR, KF and Dissolution.
- Analytical data review for development and validation data.
- Literature search and DMF review.
- CMC Group
- Regulatory documentation
share your resume on neha.modi@amnealindia.com & references are highly appreciated
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