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- ...according to business needs. Experience in: Ethylene oxide, steam, liquid chemical, and radiation sterilization methods Process Validation, Equipment IQ, and Computer software validation knowledge No sterile package design or pharma design The Personality Part...SugeridoContratoTrabajo por turnos
- ...education. Responsibilities: Responsibilities may include the following and other duties may be assigned. Conducts a compliant validation process for quality information technology systems which requires formal validation documentation (including standard operating...SugeridoTemporalTiempo completoTrabajo por turnos
- ...The Packaging Engineer will be responsible for designing, developing, validating, and optimizing packaging systems to support Product Transfer and New Product Introduction (NPI) initiatives. This role requires hands-on experience working with packaging lines, filling...SugeridoContrato
- ...Summary The Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment, process validation, and quality...SugeridoContrato
- ...The Quality Application Specialist supports product transfer activities with a primary focus on process validation, sterilization processes, and commercial release readiness. This role ensures compliant execution of validation activities and quality system requirements...SugeridoContrato
- ...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
- ...For packaging validation and testing activities in Product Transfer and New Product Introduction. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and a minimum of five (5) years of experience in the regulated industry. Excellent...SugeridoContratoTrabajo por turnos
- ...introduction of new products and manufacturing processes within a regulated medical device environment. The role focuses on equipment validation, process development, and ensuring manufacturing processes comply with regulatory and quality requirements. The engineer will...SugeridoContrato
- ...contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Must have knowledge in Process Validation, Equipment IQ and Computer software validation. Provides technical and sustaining engineering support in a manufacturing area...SugeridoTemporalTrabajo por turnos
- ...contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Conduct comprehensive packaging validation and testing activities in support of Product Transfer and New Product Introduction initiatives. Interaction with packaging...SugeridoTemporalTrabajo por turnos
- ...For Validation services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and (3) three years of experience within the Medical Devices Industry. Bilingual: Spanish and English Soft Skills: Excellent Technical...SugeridoContratoTrabajo por turnos
- ...relevant experience. ~ Experience in injection molding processes +PLUS ~ 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
- ...2 years of relevant experience in a regulated industry (medical device, pharmaceutical, or similar). Experience with process validation, equipment validation, and computer software validation (CSV). Bachelor’s degree in Engineering completed Ability to manage...SugeridoContrato
- ...skills Shift: 1st and according to business needs. Experience in: Investigation and Root Cause Analysis Skills. Process Validation, Equipment IQ, and Computer software validation knowledge Technical writing The Personality Part: ~ Our Next Piece...SugeridoContratoTrabajo por turnos
- ...Quality role to support product transfer activities. focused on process validation. WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with at least three (3) years of experience within the regulated industry. Bilingual (English &...SugeridoContratoTrabajo por turnos
- ...QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website qrcgroup.com / to learn more about our services and solutions! Job Description...ContratoTrabajar en la oficina
$73 939 - $96 116 por año
...unofficial transcripts submitted with your application. AND U.S. Coast Guard Issued Merchant Mariner Credentials (MMC): You must submit a valid, legible copy of your Merchant Mariner Credential at time of application. Your copies must include the expiration and capacity pages...Tiempo completoCASRemotoU.S. Customs and Border Protection
Ponce2 días atrás- ...Select sound techniques to solve problems and make design recommendations under direction of manager. Assess results for application, validity and conformance to specifications. Prepares and controls the capital working budget for Manufacturing Projects. Utilize...Temporal
- ...to support Manufacturing areas, New Product, Design, Introduction, Development, Transfer, Implementation, as well as Changes and Validations to existing or new products manufactured within Aibonito facilities. ~Lead and participate in multifunctional projects (ex. R&D...Temporal
- ...~Supervisar que el proceso de cancelación en el club se haga correctamente y asegurar que se escriban las notas en el sistema. ~Validar la cantidad de cobros colectados diariamente por el POS. REQUISITOS ~Bilingüe inglés/español ~1-3 años de experiencia en colecciones...ContratistaTiempo completoTrabajar en la oficinaHorario flexibleFin de semana
- ...Examine, diagnose, and correct operational problems related to the equipment in the process of manufacturing and plant building areas. Validate project to improve efficiency of the production machine. To perform this job successfully, an individual must be able to...TemporalTurno de nocheTrabajo por turnos
