Strides Pharma, Inc. Jobs in United States

The Lab Sample Coordinator performs QC laboratory sample receipt processing distribution for testing storage and reconciliation through to disposal Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. · ...

This role oversees and manages the daily operation of a packaging line. · Packaging OperationsC coordinates each Operator's responsibilities during each shift. · M monitors the packaging process to ensure schedule is met within standards. · C conducts final audit of Batch Records ...

This role oversees and manages the daily operation of a packaging line. · Coordinates each Operator's responsibilities during each shift. · Monitors the packaging process to ensure schedule is met within standards. · ...

The Manufacturing Operator III – Granulation performs functions relating to the processing of drug products. · Follows standard procedures to complete tasks; · Aplies skills and knowledge to recognize issues and increase efficiency, · throughtput and quality. · ...

Key Responsibilities · Lead and supervise operations in solid dosage manufacturing and packaging to ensure adherence to Master Formula and Master Packaging Records, SOP's, cGMP , FDA requirements. · ...

We are seeking an experienced and detail-oriented Analytical Quality Assurance Supervisor to lead our AQA operations in Chestnut Ridge, NY. · ...

Packaging Group Lead · As Packaging Group Lead at Strides Pharma Inc., you will oversee and manage daily operations of a packaging line. · Coordinates operator responsibilities during each shift. · Monitors packaging process to ensure schedule met within standards. · ...

The Senior Maintenance Technician will lead maintenance activities in a GMP-regulated pharmaceutical manufacturing environment. · ...

The Manufacturing Operator III performs functions relating to the processing of drug products, ensuring product compliance to established current Good Manufacturing Practices (cGMPs), customer requirements and in conjunction with all Standard Operating Procedures (SOPs) · Operate ...

Job Overview · The Analytical Quality Assurance Supervisor is responsible for leading our AQA operations in Chestnut Ridge, NY. This role will oversee the review and approval of analytical data, ensuring compliance with cGMP regulations. · Key Responsibilities · Manage all Analyt ...

The Manufacturing Operator III performs functions relating to the processing of drug products ensuring product compliance to established current Good Manufacturing Practices cGMPs customer requirements and in conjunction with all Standard Operating Procedures SOPs. · ...

The Chemist II performs QC laboratory chemical analyses of raw materials and finished products. · Conducts laboratory analyses according to approved test methods. · ...

The Operations Supervisor is responsible for overseeing solid dosage pharmaceutical manufacturing and packaging activities during 1st shift operations, · 7:00am to 3:30pm. · This role ensures that all production operations comply with cGMP, · safety standards,and production sched ...

The Senior Maintenance Technician will lead maintenance activities in a GMP-regulated pharmaceutical manufacturing environment ensuring reliable operation of production and facility systems. · ...

The entry-level associate supports the quality management system and documentation processes at the Chestnut Ridge site providing hands-on experience in maintaining compliance and supporting documentation workflows in a regulated environment. · ...

Job Overview · This Packaging Group Lead position oversees and manages daily operations within a packaging line ensuring compliance with cGMP regulations SOPs customer requirements quality control metrics reporting accurate record-keeping monitoring progress improving processes. ...