Cipla Usa Jobs in United States

The IT specialist role is responsible for implementing IT solutions, AI automation and Infra & Security support including Cyber security. · A minimum of a bachelor's degree in engineering, Information Technology or a related field. · ...

The QA operation specialist monitors and ensures validation and qualification of facility, utilities,equipment's processes. · QualificationsAdvanced vocational training or education in pharmaceutical manufacturing. · Bachelor's degree in pharmaceutical manufacturing or related fi ...

We are seeking an enthusiastic and detail-oriented Entry-Level EHS Specialist to join our growing pharmaceutical team.As part of the Environmental, Health, and Safety department, you will be responsible for supporting the development, implementation, and monitoring of safety prog ...

The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. · Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent recor ...

Pharma Packaging Specialist · The role requires overseeing packaging activities, ensuring adherence to quality and regulatory standards, and coordinating materials and workforce. · A bachelor's degree in pharmaceutical sciences is required for this position. · Candidates should h ...

The QA inspector is responsible for monitoring product quality through all phases of manufacturing and packaging in compliance with established procedures. · Verification of raw materials during dispensing process. · Dispensing printed packaging materials to packaging. · ...

The Analytical Quality Assurance (AQA) associate II and III position is a team or individual contributor role and reports to the Supervisor Analytical Quality Assurance for InvaGen Pharmaceuticals, Inc., a Cipla subsidiary located at Hauppauge, · New York.The job duties for this ...

A leading global pharmaceutical company is seeking an Analytical Senior Scientist for its Research & Development division in New York. The role involves developing and validating analytical test methods, overseeing analytical procedures, and collaborating with project teams. Cand ...

The job is for PLC/Electrical Automation Engineer at InvaGen Pharmaceuticals in Hauppauge, NY. · Manage all phases of electrical and control equipment throughout the plant.Diagnose and solve electrical problems for manufacturing and packaging equipment and systems.Install, servic ...

Cipla (InvaGen) Pharmaceuticals Inc. · is looking for an Analytical Senior Scientist position in Research & Development at our US facility in Central Islip, New York. · ...

The QC Sampling Associate is responsible for performing sample withdrawal for all incoming raw materials, packing materials, and updating sample information in SAP as per company procedures. · ...

A leading pharmaceutical company in Hauppauge, NY, is seeking a PLC/Electrical Automation Engineer to oversee electrical systems in manufacturing. This role involves diagnosing and solving problems with manufacturing and packaging equipment, developing maintenance procedures, and ...

The QC Chemist I will perform routine analytical testing of raw material, in-process samples and finished products to ensure they meet quality standards. · Strong analytical skills and knowledge of quality control procedures required. · ...

The Warehouse Operator III will perform various tasks including inspecting carriers/trailers of inbound and outbound shipments, escorting drivers when in the facility, receiving and unloading freight checking for damaged goods verifying items with BOL Packing List PO etc. · Moves ...

Job Title: Documentation Specialist II · Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist.The Documentation Specialist is responsible for the creation and revision of new and existing GMP batch production records as well ...

This IT specialist role is responsible for implementing IT solutions including AI automation and Infra & Security support. ...

Job summaryReconciling vendor contracts and invoices. Maintaining daily logs and activities for services provided. Processing purchase requisitions (PRs) and purchase orders (POs). Tracking and reporting vendor supplies, services, work schedules, and hours logged. · ...

QA Analyst I Role · A global pharmaceutical firm seeks a QA Analyst I to ensure analytical quality assurance compliance. · Main Responsibilities · Review laboratory documents ensuring adherence to Good Laboratory Practices · Coordinate with lab teams promoting effective collabora ...

Job Summary · A leading global pharmaceutical company is seeking a QA Associate (IT) with strong knowledge of batch documentation and attention to detail. · Reviewing batch production records for compliance with GMP and regulatory standards. · ...

The Section Head position involves controlling manufacturing activities in the respective section to ensure compliance with cGMP & safety standards. Key accountabilities include monitoring production schedules, ensuring availability of raw materials, and implementing quality cont ...