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 Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets API...
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 Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. The USA subsidiary also markets API...
POSITION DESCRIPTION. Role / Position Title. Regulatory Affairs Manager - CANADA. Country. Canada. Region / City. Vaughan, Ontario. FLSA (Exempt/Non-Exempt). Exempt. POSITION SUMMARY. Reporting to the Associate Director, Regulatory Affairs, this position is responsible for managing functional activities to ensure that the companys goals and objectives are met. This position also manages compliance within the department and ensures that global, r...
Glenmark 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 Process/Packaging equipment including Factory Acceptance Testing, User Requirement Specification, System Impact Assessment, Design ...
Job Summary. Glenmark is actively seeking a Quality Control Analyst to join the growing team in Monroe, NC. The QC Chemistry Analyst position supports the Quality Control group to maintain process optimization and manufacturing activities. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with st...
POSITION DESCRIPTION. Role / Position Title. Associate Manager, Transportation and Analytics. Department/Function. Operations. Country. USA. Region / City. (within Country) - Mahwah, NJ. FLSA (Exempt/Non-Exempt). Exempt. Hours. 8 a.m. to 5 p.m. in office 3-5 days per week. POSITION SUMMARY. The Associate Transportation Manager is responsible for coordinating and managing all transportation related functions with goal to effectively track US Comme...
Position 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 product introductions into the Monroe site. This will include activities such as scale-up batches, equipment/systems ...
POSITION DESCRIPTION. Role / Position Title. Senior Payroll and Benefits Specialist. Department/Function. Human Resources. Region / City. (within Country) - Mahwah, NJ. FLSA (Exempt/Non-Exempt). Exempt. Hours. 8 a.m. to 5 p.m. in office 3 days per week. . POSITION SUMMARY. The Payroll & Benefits Senior Specialist will oversee the organizations payroll functions, ensuring pay is processed on time, accurately, and in compliance with government regu...
The Senior Manager Quality Assurance - Data Integrity Officer (DIO) is responsible for ensuring the accuracy and reliability of cGMP data and data supporting regulatory submissions. Generally, this requires implementing, as appropriate, and overseeing systems and processes to ensure complete, consistent, enduring, and accessible data is attributable, legible, contemporaneously recorded, original or a true copy, and accurate. The Senior Manager ...
Under 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 documents according procedures. . Maintain quality system controls to ensure state of compliance. . Take appropriate steps ...
Position Summary. The Microbiology Manager reports to the Associate Director, Microbiology and primary responsibilities will be to manage and coordinate staff performing microbiological testing in support the manufacturing of aseptically processed, terminally sterilized pharmaceutical products and oral solid dosage products. Provides technical leadership, daily oversight and subject matter expertise as needed to manage the QC microbiology laborat...
As an ideal candidate, you will be responsible for performing microbiological tests that support the environmental monitoring processes in support of product manufacturing. These include routine monitoring and reading of contact plates as well as gram staining. This position also contributes to the completion of routine technical tasks. This is a Tuesday - Saturday position. Monitoring (EM) Samples and understanding of grid monitoring. . Successf...
