Medical Representative
Position: Medical Representative Company: Alembic Pharmaceuticals Limited Reference No: Field - MR9462 Location: Delhi - 5, DL Experience: 0 to 5 years No. of Vacancies: 1 Published Date: 03-Oct-2026
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Position: Medical Representative Company: Alembic Pharmaceuticals Limited Reference No: Field - MR9462 Location: Delhi - 5, DL Experience: 0 to 5 years No. of Vacancies: 1 Published Date: 03-Oct-2026
Position: Medical Representative Company: Alembic Pharmaceuticals Limited Reference No: Field - MR9591 Location: Bangalore - 3, KA Experience: 0 to 5 years No. of Vacancies: 1 Published Date: 03-Oct-2
Position: Medical Representative Company: Alembic Pharmaceuticals Limited Reference No: Field - MR9592 Location: Bangalore - 1, KA Experience: 0 to 5 years No. of Vacancies: 1 Published Date: 03-Oct-2
Position: Area Manager Company: Alembic Pharmaceuticals Limited Reference No: Field-Mgr9587 Location: Ernakulam, KL Experience: 3 to 16 years No. of Vacancies: 1 Published Date: 04-Oct-2026 Department
Position: Area Manager Company: Alembic Pharmaceuticals Limited Reference No: Field-Mgr8002 Location: Coimbatore, TN Experience: 3 to 16 years No. of Vacancies: 1 Published Date: 05-Oct-2026 Departmen
Position: Regional Manager Company: Alembic Pharmaceuticals Limited Reference No: Field-Mgr9582 Location: Vijayawada, AP Experience: 5 to 21 years No. of Vacancies: 1 Published Date: 06-Oct-2026 Depar
Description: This role is responsible for conducting in-process and final product quality analyses and inspections within a quality control laboratory in strict compliance with established standards a
Perform line clearance before starting compression activities. Verify cleanliness and status labels of compression machine, tooling, and accessories. Ensure availability of approved Batch Manufacturin
Job Description: Scientific review of Protocol and related documents i.e ICF, CRF, Plans, logs and forms, etc. as per regulatory requirements. Review of SIV presentations prepared by CRO and check for
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment.
Job Responsibility: Responsible for all activities related to warehouse at Amneal Healthcare as per their respective SOPs & as per cGMP. Responsible for receipt & dispatch of Raw materials, Packaging
Description: This role is responsible for performing a variety of tasks related to the processing and assembly of ingredients and pharmaceutical products within a regulated manufacturing environment.
Required Skills: Strong knowledge of country specific regulatory labeling requirements Understanding of packaging materials and artwork processes Familiarity with labeling software/tools Attention to
1. Technology Implementation: 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 Automation.
Description: To perform all quality control activities with compliance to cGxP for instrumental, chemical and physical analysis. Essential Functions: Perform testing of in process, finished product an
A. Business Process Understanding & Documentation Understand existing (AS-IS) finance processes across: General Ledger Accounts Payable Accounts Receivable Asset Accounting Bank Accounting Period Clos
Description: This role is responsible for creating, reviewing, and maintaining technical documentation related to quality control processes and activities in compliance with established standards and
Good knowledge of US ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. Exposure of the Solid oral dosage form/Liquid Oral/Transdermal dosage form / topical-
Description: Responsible for managing regulatory affairs activities and regulatory strategy execution to ensure compliance with global regulatory requirements, industry standards, and ethical practice
Good knowledge of ANDA submission activities and post-approval procedures and related ICH and USFDA guidelines. API DMF and DMF Change Notification review with respect to USFDA regulatory requirement.
Looking for something specific?
Browse all job categories →