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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 completoRemotoTrabajo híbrido
- ...plazo. Funciones: Acercarse a la zona asignada por el supervisor para visitar diversos establecimientos comerciales. Validar que las tiendas cumplan con los requisitos establecidos por la compañía. Informar a los propietarios o gerentes de las tiendas...SugeridoLunes a viernes
- ...Prepare and maintain accurate documentation, schematics, and records of electrical systems, maintenance, and modifications. Support validation and qualification activities for electrical equipment in regulated environments. Participate in audits and inspections,...SugeridoTiempo completo
- ...from leader and team members, and commits to self-development; has an Individual Development Plan in place. Obtains and maintains valid pharmacy technician license as required by state. Communications Communicates regularly with team members through one-on-one...SugeridoPrácticaTemporalTrabajo por turnosFin de semana
- ...Shift Location: Villalba, PR Education: Bachelor's degree required in Engineering Preferred Qualifications: * Process Validation, Equipment IQ and Computer software validation knowledge * Technical writing knowledge and Communication skills *...SugeridoTiempo completoContratoTrabajo por turnos
- ...Puerto Rico & USA. Responsibilities: Change control of Medical Devices Equipment Commissioning / Qualification Process Validation Computer System Validation (CSV) Manufacturing, Packaging and Laboratory Equipment Technical experience (Trouble shooting...SugeridoTemporalTurno de tardeTrabajo por turnos
- ...~ 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
- ...deployment, and Control Plans for new products. * Define Receiving Inspection requirements as required and associated test method validation for all internal Test Methods. Shift: Administrative Location: Villalba, PR Education: Bachelors degree required in...SugeridoTiempo completoContratoTrabajo por turnos
- ...manufacturing industry in Puerto Rico & USA. Responsibilities: Support product transfer activities, mainly focus on process validation and release product up to commercial release. Conducts a compliant validation process for quality information technology...SugeridoTemporalTrabajo por turnos
$58 500 - $93 600 por año
...is complete! Ability and willingness to travel approximately 75% as required. Ability and willingness to possess and maintain a valid passport and driver's license. ABB is an Equal Employment Opportunity and Affirmative Action employer for protected Veterans and...SugeridoTemporalTiempo completoTrabajar en la oficinaRemotoLunes a viernes- ...and English Soft Skills: Excellent teamwork skills Shift: 1st, and according to business needs. Experience in: Process Validation Equipment IQ and Computer software validation knowledge Technical writing knowledge and Communication skills...SugeridoContratoTrabajo por turnos
- ...to business needs. Experience in: Knowledge of GMP in a manufacturing environment. Experience with equipment and process validation. Ability to perform risk assessments and risk analysis. The Personality Part: ~ Our Next Piece is someone who treats...SugeridoContratoTrabajo por turnos
- ...Shift: 1st, and according to business needs. Experience in: Knowledge on Sterilization Knowledge in Final Pack Process Validation, Statistical Analysis, Process Failure Mode and First Time Quality The Personality Part: ~ Our Next Piece is someone...SugeridoContratoTrabajo por turnos
- ...deployment, and Control Plans for new products. Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods. Qualifications: ~ Bachelor's degree in Engineering. ~2 years relevant experience...SugeridoTemporalInicio inmediatoTurno de mañana
- ...teamwork skills Shift: 1st, and according to business needs. Experience in: Process Development and documentation Equipment validation SOP Development Special Build Documentation and Line Support The Personality Part: ~ Our Next Piece is someone...SugeridoContratoTrabajo por turnos
- ...product transfer activities within a regulated medical device manufacturing environment, with primary responsibility for process validation and product commercialization efforts. This role ensures compliance of quality systems, manufacturing processes, and computerized...ContratoTrabajo por turnosFin de semana
- ...manufacturing sites. The most widely used are Equipment Controller (EC) and External Functions (EF). Both of these components are validated using the Global IT MSCM Procedure. All documentation from MSCM is leveraged into CSV. However, CSV has one extra step that is...TemporalTrabajo por turnos