CIPLA LTD Jobs in United States

Job summary · The QA Associate (IT) is responsible for review of batch production records to ensure their integrity, accuracy, and completeness. · QualificationsBachelor's degree in pharmacy or related field. · ...

The Quality Control Lab Technician performs sample withdrawal for all incoming raw materials and updates information in SAP as per company procedures. · ...

The purpose of this role is to assist in the warehouse operations of a pharmaceutical manufacturing company. · Responsible for receipt and dispensing of Raw materials and Packing materials. · Receiving and storing finished goods and miscellaneous items. · ...

The QA Specialist will drive strategic imperatives and operational performance of quality assurance function at external manufacturing site ensuring implementation of quality systems successful delivery of business strategy while adhering to regulatory compliance. · ...

About this role · This Packaging Operator II position is responsible for performing various tasks related to packaging operations in a cGMP environment. · Perform all functions according to current Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP ...

This is a highly visible individual contributor role that reports to the Director of Project Management. · The Project Manager position is responsible for end-to-end project leadership and management (scope, cost and time) deliverables for Cipla projects. · ...

The IT-QA Associate position is responsible for accurately reviewing electronic data related activities in a pharmaceutical manufacturing organization. · Function as SME for IT related activities of QMS platforms and other electronic systems. · Conduct regular audits of the audit ...

Job Summary: · This Manufacturing Specialist role involves assisting in coordinating daily packaging activities to meet production schedules of projects. · Monitor packaging processes for adherence to cGMP, FDA, and Cipla's quality standards.Identify and resolve operational ineff ...

The content and statements documented in this job description are designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. · Develops appropriate d ...

The purpose of this role is to assist in packaging manufactured metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. · The scope (content and statements) of this job description is designed to describe the general nature and level of work as well as p ...

The Site Services Administrator II (Vendor Relations and Payments) will reconcile vendor contracts and invoices, maintain daily logs and activities for services provided, process purchase requisitions (PRs) and purchase orders (POs), track and report vendor supplies, services, wo ...

The Environmental Health and Safety Site Manager develops implements oversees program changes for workplace health safety.Serve as subject matter expert in areas of environmental health safety specialization interact with internal external customers. · Develop hazardous chemical ...

The QA QMS Associate position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Quality Team. This role ensures compliance with both internal and external quality standards at Invagen Pharmaceuticals Inc. Fall River Facility. · ...

The purpose of this role is to assist in manufacturing and packaging metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. ...

The job of the Chemist is an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. · ...

Esta posición requiere un fuerte conocimiento en química analítica/laboratorio y experiencia. Las responsabilidades del puesto incluyen revisar e informar sobre la conformidad relacionada con materiales brutos, productos intermedios y documentos analíticos finales. · ...

The job of the “Chemist” is simple described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. · ...

+The purpose of this role is to be part of manufacturing metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. · ...

This IT specialist role is responsible for implementing IT solutions, AI automation and Infra & Security support including Cyber security. · Build technical understanding of MES applications, Serialization Software's, Quality Systems QC applications/software's and end to end busi ...

+ Manufacturing Process Associate · + Job Title: Manufacturing Process Associate · + Organization Name: InvaGen Pharmaceuticals, Inc., a Cipla subsidiary. · + Location: 550 South Research Place, Central Islip, NY 11722.Lead process capability improvement · Drive manufacturing ...