Jobs: glenmark pharmaceuticals

Senior IT Associate Department: IT Location: Monroe, NC START YOUR APPLICATION (rmdirect.com/resumedirect/ApplyOnline/Apply.aspx?req\_id=3048620&source=3048620-CJB-0) Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules - both New Chemical Entities (NCE's) and New...

Job DescriptionJob DescriptionGlenmark is actively seeking a Senior Validation Specialist to join the growing team in Monroe, NC. Planning the site validation activities to meet organizational business requirements and regulatory specifications. Responsible for preparing and executing qualification documents for a variety of Utility, Facility and...

Job DescriptionJob DescriptionGlenmark is actively seeking a Senior Validation Specialist to join the growing team in Monroe, NC. Planning the site validation activities to meet organizational business requirements and regulatory specifications. Responsible for preparing and executing qualification documents for a variety of Utility, Facility and...

Job DescriptionJob DescriptionPosition Summary:Glenmark is actively seeking a Senior Specialist, MSAT to join the growing team in Monroe. The Sr. Specialist, MSAT will provide technical expertise to optimize commercial manufacturing processes and commercialize new products and technologies. This role is responsible for performing project activities for new...

Job DescriptionJob DescriptionGlenmark is a leading player in the discovery of new molecules both NCEs (new chemical entity) and NBEs (new biological entity) with eight molecules in various stages of clinical development. The company has a significant presence in branded generics markets across emerging economies including India. Its subsidiary, Glenmark...

Reporting to the Associate Director, Regulatory Affairs, this position is responsible for managing functional activities to ensure that the company s goals and objectives are met. This position also manages compliance within the department and ensure Regulatory Affairs, Manager, Regulatory, Health, Clinical, Pharmaceutical, Business Services

Job DescriptionJob DescriptionUnder the direction of the QA Document Control Supervisor, the QA Specialist – Document Control, will control the movement, filing, archiving, and securing of all documents with the objective of ensuring compliance to company policies and procedures. In addition, the QA Specialist will review, issue, and reconcile controlled...