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- ...Engineers with at least three (3) years of experience in Medical Device or Pharmaceutical industries. The role will focus on executing validation protocols (IQ, OQ, PQ), troubleshooting, and optimizing manufacturing processes. Responsibilities: Develop and execute...SugeridoContratistaTiempo completo
- ...with Microsoft Excel, Word, and Microsoft Office. Bilingual communication skills in English and Spanish, written and verbal. Valid driver's license. Ability to travel to customer and project sites as required. Willingness to work in both office and industrial...SugeridoTiempo completoTrabajar en la oficina
- ...issues, specifications, and inspection procedures questions at the incoming inspection area. Experience evaluating, selecting, validating and qualifying equipment / tools/ technologies for accurate inspection, including fulfilling financial requirements for capital...SugeridoContratistaTiempo completo
- ...Raw Materials, In-Process Materials, Finished Products, Stability Programs, and Method Transfers. You will also oversee laboratory validation activities, quality monitoring programs, and change control processes to support business priorities, quality objectives, and...SugeridoTemporal
- ...Troubleshoot daily quality and material issues to support safe and efficient product release. Participate in new product protocols and validation activities. Perform drug inventory head counts according to established procedures. Support Manufacturing operations in the...SugeridoTemporalHorario flexibleTrabajo por turnosFin de semana
- ...according to business needs. Experience in: Computer proficiency Problem-Solving Techniques Root Cause Analysis Process Validation and Computer Software. The Personality Part: ~ Our Next Piece is someone who treats everyone they meet like family,...SugeridoContratoTrabajo por turnos
- ...technical information, understand the impact of changes in values, and make sound decisions. Bilingual in Spanish and English. Valid Puerto Rico driver's license. Availability to work overtime, weekends, and night shifts, as operational needs require....SugeridoTemporalTiempo completoTurno de nocheFin de semana
- ...~ Bachelor’s degree in Engineering ~3+ years of relevant experience. ~ Process Development and documentation ~ Equipment validation ~ SOP Development ~ Special Build Documentation and Line Support ~ Experience in equipment IQ |Experience in OQ (Operational...SugeridoTemporalTrabajo por turnos
- ...enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating...SugeridoTemporalTrabajar en la oficinaTrabajo por turnos
- ...opportunities for improvement, efficiency, quality, and productivity. Support equipment installation, qualification, process validation, and implementation activities. Develop and maintain process documentation, procedures, and technical reports. Participate...SugeridoTemporalTurno de mañana
- ...Troubleshoot daily quality and material issues to support safe and efficient product release. Participate in new product protocols and validation activities. Perform drug inventory head counts according to established procedures. Support Manufacturing operations in the...SugeridoTemporalTrabajo por turnosFin de semana