/ 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

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

The overall objective of the Production Planner is to prepare and execute production plans, coordinate, and expedite workflow across departments in conjunction with daily/weekly/monthly production schedules. This position solves day to day operational issues to facilitate delivery of the overall manufacturing business plan. Scope The Production Planner is an individual co

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

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. Scope InvaGen Pharmaceuticals is searching for experienced candidates for the position of Manufacturing Documentation

/ 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

/ 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

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. Scope Invagen Pharmaceuticals is searching for experienced candidates for the position of Human Resources intern. Inva

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

The purpose of this role is to assist in the mechanical/electrical maintenance, repairs and servicing of a pharmaceutical manufacturing facility. 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

The QC Intern is responsible for performing test of samples of various types using various techniques or equipment in the QC laboratory in compliance with established specifications. The role may be further modified based upon individual education, training, experience or a combination of all three. ESSENTIAL FUNCTIONS The responsibilities of the QC Intern include but are

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

The purpose of this role is to assist in manufacturing metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Manufacturing Line Lead (Requirement 3 10 years of MFG Experience or Management Approval) Scope The Manufacturing Line Leader position is a group contributor role and reporting to Supervisor or Manager of Manufacturing Operations at Inva

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

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 including but not limited to vendor relationships, and managed services for non GMP business related support operations. The role will hel