/ Accountabilities Enforce compliance of current Good Manufacturing Procedures standardsincluding proper identification, segregation and staging of materials. Interpret and enforce safety, quality, health and personnel regulations. Coach, direct, develop and train team members and supervisors. Effectively manage employee relations within assigned area. Facilitate team impr

/ Accountabilities Should have minimum 6 months experience independently operating a variety of coating pans 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.) Exe

Perform all functions according to current Good Manufacturing Practices (cGMP) and company Standard Operating Procedures (SOP). Perform installation, repair and troubleshooting of process equipment as required, including electrical, pneumatic & electronic and mechanical systems. Efficiently maintain operating machine and correct any malfunctions. Perform schedule preventi

InvaGen Pharmaceuticals, Inc. internship program is designed to offer a rewarding experience for the candidate, which will help add real world experience to their resume, as well as provide a fresh outlook and feedback on our current practices and processes. To be a strong candidate for an internship, you should understand the principles and concepts for the discipline fo

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

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

InvaGen Pharmaceuticals, Inc. internship program is designed to offer a rewarding experience for the candidate, which will help add real world experience to their resume, as well as provide a fresh outlook and feedback on our current practices and processes. To be a strong candidate for an internship, you should understand the principles and concepts for the discipline fo

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

The Manager, Humans Resources & Compliance will be instrumental in supporting the employee life cycle for Cipla USA employees and other groups as assigned. They will partner with the Key Business stakeholders, COEs, and the HR colleagues to deliver HR Strategies seamlessly in line with the business needs and priorities. In addition, the role will be to manage HR complianc

/ 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

/ 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

/ Accountabilities Ensures that Packaging Operators under his/her lead render the highest productivity (Process Reliability). Ensure that operations are completed in the most efficient manner and so that final products meet the standards of quality required. Coordinate with Packaging Supervisor daily for production goals for his/her packaging line. Monitor and prepare dail

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

/ 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

The purpose of this role is to assist in the warehouse operations of 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 assigned to perform the job. This jo