Amneal Pharmaceuticals
Regulatory Submissions & Documentation. Prepare, review, and submit high‑quality regulatory dossiers (IND/IMPD, BLA/MAA, ANDA/Abbreviated MAA where applicable) for…
This role is responsible for overseeing in-process and final product quality analyses and inspections within the quality control laboratory in compliance with…
This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated…
Monitor and ensure adherence to enterprise data management procedures and standards. Enter / update master and reference data for assigned data domains (Products…
This role is responsible for defining and specifying the activities, processes, and standards required to fulfill quality requirements for manufactured materials…
The incumbent is responsible for managing and leading IT business analysis activities to support business strategy and operational excellence. The role focuses on…
Manage and coordinate technical writing activities for manufacturing SOPs, batch records, work instructions, and other GMP-critical documents. Implement and manage…
The role is responsible for leading and supervising pharmaceutical packaging operations to ensure quality, compliance, efficiency, and throughput across packaging…
The role is responsible for planning, designing, executing, and maintaining civil and structural infrastructure across pharmaceutical facilities. The role ensures…
Responsible for assisting in the implementation of environmental, health, and safety (EH&S) programs to ensure compliance with workplace safety regulations…
Responsible for all activities related to warehouse at Amneal Healthcare as per their respective SOPs & as per cGMP. Responsible for receipt & dispatch of Raw…
This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated…
This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated…
Cordinate and lead for all existing and future Industry 4.0 Use cases under implementation or planned in future as per guidance from Head, Digitalisation and…
We are looking for Upstream & Downstream Process Specialist for our Biosimilar manufacturing facility based out of Ahmedabad. Following are the Details of the Job…
The document control specialist is responsible for administering the processes and practices which support documentation compliance. The Specialist will work in a…
This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated…
Design, develop, test, debug, document, and support SAP ABAP developments. Reports and interfaces. Enhancements and user exit. BAdIs and enhancement frameworks…
Ensure compliance with the Gujarat Prohibition Act, 1949, and applicable excise regulations concerning industrial alcohol and regulated substances. Manage statutory…
This role is responsible for managing and overseeing injectable manufacturing operations within a regulated pharmaceutical manufacturing environment, ensuring the…
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