10 Gmps Jobs

You will be responsible for overseeing all finished goods labeling, filling, packaging, and case sealing procedures in an efficient manner that complies with state regulations, GMPs, SOPs, and all applicable packaging procedures. You will create and oversee the packaging strategy, including sourcing equipment and materials. Additionally, your role will involve ensuring a clean environment by removing debris and processing waste after extraction activities are complete. Key Responsibilities: - Set any required activity performance counts - Supervise Packaging Associates as part of a high-performance team - Assist in preparing reports, planning budgets, setting production schedules, pricing pr...

Our vision is to transform how the world uses information to enrich life for all . Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. JR58138 GEL Staff engineer Develops, evaluates, revises, and applies technical quality assurance protocols/methods to inspect and test in-process raw materials, production equipment, and finished products. Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations. Performs analysis and identifies trends in the inspection o...

As the CMO Quality Head at Sun Pharmaceutical Industries Ltd, your primary responsibility will be to provide strong leadership and oversee the Quality operations for both India CMO and US CMO. This includes ensuring QA oversight for all contract manufacturing sites based in India and engaged in manufacturing SUN products for India, ROW, EM markets through various business models like LL, P2P, and In-licensing. Additionally, you will be responsible for QA oversight for all contract manufacturing sites based in India and engaged in manufacturing SUN products for the US market through various business models like LL. Your essential job functions will include ensuring the availability and period...

You will be responsible for overseeing the production of beverages at our manufacturing facility in Bhopal. Your main duties will include planning and directing the production process to ensure the products are made safely and consistently meeting quality standards. Your role will involve supervising and coordinating the activities of production supervisors to meet production requirements and ensure the efficient operation of their respective areas. You will be in charge of production planning, process control, troubleshooting, and ensuring compliance with regulatory requirements. Key responsibilities will include reviewing and approving production documents, ensuring compliance with GMP reg...

As a Machine (Tetra Pak) Operator in the Dairy Industry located in Bahjoi - 244410, Sambhal (U.P.), your role within the Production/Packaging department will involve operating Tetra Pak machinery to ensure efficient, hygienic, and high-quality production of milk and dairy products. You will be responsible for setting up, running, monitoring, and troubleshooting production/packaging lines. Your key responsibilities will include operating and monitoring Tetra Pak auto-mode processing machines, performing machine setup and routine adjustments, monitoring packaging quality, troubleshooting mechanical or process issues, maintaining accurate production records, performing daily cleaning and mainte...

At Lilly, you play a crucial role in uniting caring with discovery to enhance the lives of people worldwide. As a global healthcare leader based in Indianapolis, Indiana, our mission is to develop and deliver life-changing medicines, enhance disease management, and contribute to our communities through philanthropy and volunteerism. Our dedicated team prioritizes people and is committed to making a positive impact on a global scale. As an Engineer Serialization Lead within the Global Serialization Program (GSP), you will oversee the implementation of serialization systems on new packaging lines across existing and new sites. Your responsibilities will involve collaborating with Engineering a...

As a production worker, you will be responsible for ensuring the cleanliness and hygiene of the production areas. Your duties will include checking tanks and equipment to ensure they are clean before the production process begins. It is essential to label tanks with the FG material number, description, and batch number accurately. You will be required to weigh, blend, and record raw material numbers precisely on the shop floor paper. Additionally, you must use personal protective equipment (PPE) and adhere to HACCP/GMP requirements. You may also be assigned other tasks as needed. In this role, you will operate electric and/or gas sit-down and stand-up reach trucks as necessary. Operating var...

Job Description The scope of work for this role is to provide QA Validation support to validation activities associated with of Laboratory instruments and Manufacturing equipment in pharmaceutical industry. The responsibility includes review and approval of Qualification/Validation documentation DQ,IQ,OQ,PQ including Risk assessment, specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the sites data integrity initiative. Successful candidate requires a strong working knowledge of global cGMP with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 2...

Job Description REMOTE OPPORTUNITY!!!!!!!! Client: Technology GCC for Global Biotech Company 2+ years of relevant experience in leading teams in the development and support of IT systems Development in a GxP biotech or pharmaceutical environment 2+ years of process improvement experience, especially experience that leverages technology as part of the solution. 2+ years experience working in a regulated environment with knowledge of GMPs, GDPs. Exceptional Interpersonal, Verbal and Written Communication Strong Leadership Skills Including Ability to Inspire and Motivate Team Members Ability to Keep Track of Various Activities in Multiple Systems Task Delegation Strong Analytical / Problem-Solv...

Job Description The scope of work for this role is to provide QA Validation support to validation activities associated with of Laboratory instruments and Manufacturing equipment in pharmaceutical industry. The responsibility includes review and approval of Qualification/Validation documentation DQ,IQ,OQ,PQ including Risk assessment, specifications, executed protocols, summary reports, deviations, periodic reviews, procedures, and change controls. In addition, this role may provide support to the sites data integrity initiative. Successful candidate requires a strong working knowledge of global cGMP with an emphasis on validation lifecycle including computer system validation, 21 CFR Parts 2...