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The purpose of this role is to assist in packaging manufactured metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Scope The scope (content and statements) of this job description is 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
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 2 days ago
Cipla USA
- Fall River, MA
The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes specific testing group. T
Posted 2 days ago
The purpose of the QA operation specialist (MDI) position is to monitor and ensure validation and qualification of facility, utilities, equipment's, processes and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs) and to provide guidance to QA associ
Posted 2 days 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 2 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 3 days ago
/ Accountabilities Manage shifts and controls activities in absence of the Packaging Manager. Supervises activities and work performed on the floor. Supporting Line Leaders and other employees when necessary. Maintaining and enforcing proper cGMP practices across all work areas. Responsible for working in all areas such as Pre check and office duties. Responsible for worki
Posted 3 days ago
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. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qual
Posted 4 days ago
Invagen Pharmaceuticals is searching for experienced candidates for the position of Lead Pharmaceutical Production Technologist. This person will manage the production staff and oversee the production processes. Scope The Lead Pharmaceutical Production Technologist ensures compliance with cGMP's, InvaGen Pharmaceutical's policies, standard operating procedures, and FDA re
Posted 4 days ago
The purpose of the Quality Assurance Production Lead (QMS) is to monitor and ensure product quality is maintained throughout all phases of the manufacturing process in compliance with established specifications and standard operating procedures (SOPs) and to [provide guidance to Quality Assurance associates. Scope The Quality Assurance Production Lead (QMS) is an individu
Posted 4 days ago
InvaGen Pharmaceuticals, Inc. is searching for experienced candidates for the position of Packaging Supervisor Scope The Packaging Supervisor ensures compliance with cGMP's, InvaGen Pharmaceutical's policies,standard operating procedures, and FDA requirements. The incumbent will serve as a key resource forconducting product complaints, supporting packaging, and packaging
Posted 4 days ago
of Responsibilities Dispensing raw material and primary packing materials as per work order. Ensure proper planning and execution of Batch Manufacturing Records and SOP. Monitoring, cleaning and sanitation of production area and machinery as per respective SOP. Conducting in process checks, on line documentation, and timely recording entries related to manufacturing and fi
Posted 4 days ago
Cipla USA
- Fall River, MA
The job of the Environmental Health and Safety Specialist "EHS Specialist" is described as an individual contributor who develops, implements, and oversees program changes for workplace health and safety. This person also interprets policies and procedures as they apply to environmental health and safety practices. Scope The scope (content and statements) of this job desc
Posted 4 days ago
/ 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 4 days ago
The purpose of this role is to assist in manufacturing and packaging metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Scope The scope of this job description is 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
Posted 4 days ago
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