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/ Accountabilities The QA Inspector is responsible for monitoring and ensuring product quality is maintained through all phases of manufacturing or packaging in compliance with established specifications. Perform in process testing (e.g., weight, thickness, hardness, disintegration, friability, etc.) as per manufacturing batch record instructions. Perform room and equipmen
Posted 1 day ago
Lead and execute the strategy for balancing supply and demand across the organization for selected portfolio of products. Manage and facilitate all facets of supply planning activities among departments and sites supporting the market. Support strategic plans to improve productivity, quality and efficiency. Responsibilities & Accountabilities Supply Chain Planning & Execu
Posted 1 day ago
Performs and oversees cGMP compliance based services (qualification, validation, APQR, etc.) on equipment and facilities and utilities associated with pharmaceutical manufacturing and drug product development. Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale up, engineering and validation studie
Posted 1 day ago
/ Accountabilities This position is an individual contributor role and a member of the InvaGen Pharmaceuticals Plant Manufacturing Operations Team. The position reports to the Manager of Production Planning and maybe matrixed to other functional leaders within Manufacturing Operations. The overall objective of this position is to prepare and execute production plans, coord
Posted 1 day ago
Develop and implement customer engagement strategy across the entire Federal Healthcare landscape, such as VA, Department of Defense (DoD), Indian Health Services (HIS), and BoP. Identify each major procurement facility for Federal Healthcare procurement, including the seven (7) main CMOPs for the VA. Ensure there is a clear communication chain laid out for each of those
Posted 1 day ago
Over the last eight decades, Cipla has strengthened leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the United States, and other economies of the emerging world. Driven by the vision, none shall be denied, Cipla's focus has alway
Posted 1 day ago
/ Accountabilities The job duties for this position include but are not limited to the following Operate as the subject matter expert (SME) on analytical methods for products that are under development, products that are commercialized and in support of process analytical technologies (PAT) for commercial manufacturing processes. Operate as the subject matter expert (SME)
Posted 1 day ago
/ Accountabilities Organize and oversee the activities related to the manufacturing of tablets and capsules to include delivery, in process samples in a defined schedule. Review and compile the documents generated during the production of tablets and capsules such as Batch Manufacturing Record (BMR), PQ protocol. Perform SAP entry during and finish batches product. Make eq
Posted 12 days ago
/ 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
Posted 12 days ago
This position provides support to the Site Services Department through the development of continuously improving processes, aggregating and analyzing data, managing vendor relationships through their entire life cycle including, onboarding, day to day transactions and assisting in the processing of data and financial requirements for critical to business operations. Respo
Posted 20 days ago
This position reports to the Head of Administration & Site Services. The individual performing this supervisory role will manage and oversee the daily field support for vendor managed services and other operational activities and tasks to include but not limited to vendor relationships, and managed services for non GMP business related support operations. The role will he
Posted 20 days ago
/ 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
Posted 21 days ago
Cipla USA
- Central Islip, NY
/ Accountabilities The 'R&D Scientist, Sterile Injectable/Parenteral/Solid Oral Formulations' position is an individual contributor role and reporting to the Director of Research & Development (R&D) at InvaGen/Cipla New York. The job duties for this position include but are not limited to the following Operate as the subject matter expert (SME) on pre formulation and formu
Posted 1 month ago
Cipla USA
- Central Islip, NY
The QA Validation Associate role is responsible for providing Quality Assurance support for receiving/ releases GMP documentation of bulk drug substances and finished drug products. Responsibilities include but are not limited to GMP documentation review and supporting other QA functions as needed. In this role, the individual is responsible for continuously monitoring sy
Posted 1 month ago
Project Management Lead, R&D Posting Date Apr 19, 2024 Country United States State New York Location Central Islip Req Id 84016 Project Management Lead, R&D Central Islip, NY Works under the supervision of the Director of Project Management. This position is responsible for handling R&D activities under Life Cycle Management, organizing meetings with all right stakeholder
Posted 2 months ago
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