/ Accountabilities Enforce compliance of current Good Manufacturing Procedures standardsincluding proper identification, segregation and staging of materials. Interpret and enforce safety, quality, health and personnel regulations. Coach, direct, develop and train team members and supervisors. Effectively manage employee relations within assigned area. Facilitate team impr

/ Accountabilities Should have minimum 6 months experience independently operating a variety of coating pans Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Exe

Perform all functions according to current Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP). Perform installation, repair and troubleshooting of process equipment as required, including electrical, pneumatic & electronic and mechanical systems. Efficiently maintain operating machine and correct any malfunctions. Perform schedule preventi

/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record

/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record

/ Accountabilities Ensures that Packaging Operators under his/her lead render the highest productivity (Process Reliability). Ensure that operations are completed in the most efficient manner and so that final products meet the standards of quality required. Coordinate with Packaging Supervisor daily for production goals for his/her packaging line. Monitor and prepare dail

Project Management Lead, R&D Posting Date Apr 19, 2024 Country United States State New York Location Central Islip Req Id 84016 Central Islip, NY hypothesis driven investigations for quality events (planned and unplanned deviations) with recommendations of relevant corrective and preventative actions (CAPAs) to relevant stakeholders. Maintain effective and pro active comm

/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record

/ Accountabilities Conduct focused time studies to support packaging operations. Apply complete knowledge of process improvement strategies and lean techniques (e.g. Method analysis, work combination charts, ergonomics, visual controls, safety, 5S, Kanban, poka yoke) to analyze and improve overall packaging operations. Perform and direct data mining and analyze the results

This individual will manage and oversee Site Services support related tasks, vendor relationships, and managed services for non GMP business related support operations. The role will plan and manage projects, develop and implement documented processes to manage costs, and qualitatively improve the variety of services needed to keep the site operational and support the fac

/ Accountabilities Inspect carriers/trailers of inbound and outbound shipments and report to WH Coordinator any discrepancies. Escorts drivers always when in the facility and ensure gowning procedures are followed. Receives and unloads freight, checks for damaged goods, verifies items and quantities received with BOL, Packing List, PO, etc. Moves materials as required for

/ Accountabilities Must be willing to work in a pharmaceutical manufacturing setting. Must be able to know how to operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.) Execute procedures for manufacturing processes in accordance with batch manufacturing record

/ Accountabilities Inspect carriers/trailers of inbound and outbound shipments. Escorts drivers always when in the facility. Receives and unloads freight, checks for damaged goods, verifies items and quantities received with BOL, Packing List, PO, etc. Moves materials as required for sampling, inspection, status label changes, etc. Move materials from Quarantine to Release

/ Accountabilities The purpose of this position is to serve as an Analytical Quality Assurance (AQA) Associate. This role will report to the Section Head of Analytical QA or other senior leaders in the Quality organization at InvaGen Pharmaceuticals, Inc. This role will be part of the Cipla NY (Invagen) Quality Control (QC)/Analytical QA Team whose role is to ensure our pa