RECUBRIDOR/A MANUAL ALIMENTACIÓN - IMAN TEMPORING ETT - Santa Perpètua de Mogoda

En Santa Perpètua de Mogoda, se necesita personal para cubrir un puesto de mozo o moza de almacén en una empresa del sector farmacéutico.Las tareas principales incluyen carga y descarga de mercancías, movimiento de productos tanto manualmente como con transpaleta eléctrica, así como labores de

Se necesita una persona para trabajar en el almacén, con experiencia en el manejo de carretilla elevadora. Las funciones principales serán la recepción de mercancías, su correcta ubicación, la preparación de pedidos y la expedición de los mismos. Es fundamental tener un año de experiencia como carretillero. Aunque no se requieren estudios específicos, sí es indispensable contar con la formación pertinente para el manejo de maquinaria de almacén. Se busca a alguien que pueda trabajar en un entorno de ritmo ágil y que siga las pautas marcadas para garantizar la seguridad y la eficiencia. La jornada laboral será rotativa, con turnos de mañana y tarde, adaptándose a las necesidades de la producción. Se ofrece una oportunidad para formar parte de una empresa estable en el sector de la automoción, contribuyendo a sus operaciones logísticas.

¿Buscas trabajo en industria y producción? Este mes de julio surgen nuevas oportunidades para operarios en Santa Perpètua de Mogoda. ¡Inscríbete gratis hoy mismo!

ph3Quality Assurance Technician /h3 h3Main Activities And Responsibilities /h3 ul liReview and sign the Certificate of Analysis for Customers, checking CSO when applicable /li liReview and test preparation shipments /li liManage internal quality audits and Good housekeeping and propose improvement actions to achieve quality standards /li liPrepare reports which reflect relevant issues related to the quality of manufactured products /li liManage and participate in staff GMP training program from all departments /li liControl research documentation for investigating mistakes, process change and recovering process /li liDevelop and coordinate Validation Plan and Revalidation /li liSupervise the implementation of stability studies /li liTrack periodic calibrations of plant’s instrumentation /li liAchieve objectives related to GMP and Good Housekeeping improvements (internal quality audits, validation plans, document control) /li liPrepare annual product reviews according to the products manufactured /li liUpdate Sops for the Quality Management Department /li liReview methodical analytics /li liPrepare for new processes VMP /li liKey user of SAP and other IT quality systems (Quality environment) /li liParticipate in projects, committees and subcommittees representing QA role /li /ul h3Ideal Candidate /h3 ul liBachelor degree /li liFluent in both English and Spanish /li liKnowledge of audit quality procedures /li liKnowledge of Quality Control (QC), particularly in the management of OOS /li liMinimum of 2 years of experience in a similar role /li /ul h3Terms and Reward /h3 pWe offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals. The organization is very flat. You have a lot of freedom and responsibility in an open, direct, and informal atmosphere. /p /p #J-18808-Ljbffr

Centrient Pharmaceuticals is seeking a Quality Assurance Technician in Cataluña, Spain. The role involves reviewing COAs, signing off on CSOs, validating shipments, and managing internal quality audits to ensure GMP-compliant operation.

Centrient Pharmaceuticals is the leading manufacturer of beta‑lactam antibiotics, and a provider of next‑generation statins and anti‑fungals. We produce and sell intermediates, active pharmaceutical ingredients and finished dosage forms. La descripción completa del puesto cubre todas las habilidades asociadas, la experiencia previa y cualquier cualificación que se espera que tengan los solicitantes. We stand proudly at the centre of modern healthcare, as a maker of essential and life‑saving medicines. With our commitment to Quality, Reliability and Sustainability at the heart of everything we do, our over 1.600 employees work continuously to meet our customers’ needs. We work towards a sustainable future by actively participating in the fight against antimicrobial resistance. Founded 150 years ago as the ‘Nederlandsche Gist‑en Spiritusfabriek’, our company was known as Gist Brocades. Headquartered in Rotterdam (Netherlands), we have production facilities and sales offices in China, India, the Netherlands, Spain, the United States and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, a leading global private investment firm. Quality Assurance Technician The main activities and responsibilities • Review and sign the Certificate of Analysis for Customers, checking CSO when applicable., • Review and test preparation shipments., • Manage internal quality audits and Good housekeeping and propose improvements actions to achieve quality standards., • Prepare reports which reflect relevant issues related to quality of manufactured products., • Manage and participate to staff GMP's training program from all departments., • Control research documentation for investigating mistakes, process change and recovering process., • Develop and coordinate Validation's Plan and Revalidation., • Supervise the implementation of stability studies., • Tracking periodic calibrations of plant's instrumentation., • Achieve objectives related to the standards GMP and Good Housekeeping improvements (internal quality audits, validation plans, document control)., • Prepare annual product reviews according to the products manufactured., • Update Sop's Quality Management Department., • Review methodological analytics., • Prepare for new processes VMP., • Key user's SAP and other IT quality systems (Quality environment)., • Participate on project, committees and subcommittees representing QA role. The Ideal Candidate • Bachelor degree., • Fluent in both English and Spanish., • Knowledge of audit quality procedures., • Knowledge of Quality Control (QC), particularly in the management of OOS., • Minimum of 2 years of experience in a similar role. Terms and reward We offer a local contract in a challenging, comprehensive, operational environment, with many opportunities for personal input and growth and plenty of discussions with other professionals. The organization is very flat. xcskxlj You have a lot of freedom and responsibility in an open, direct, and informal atmosphere. #J-18808-Ljbffr