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- ...English & Spanish). Project Management skills. Shift: Administrative, and according to business needs. Experience in: CQV Validation Expert: Risk-based qualification methods (ASTM E 2500) for pharmaceutical manufacturing equipment and utilities Sterilization...SugeridoContratoTrabajo por turnos
- For Packaging services in the Engineering area WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree in Engineering with five (5) years of Engineering experience within the pharmaceutical or medical device industry. Bilingual (English & Spanish). ...SugeridoContratoTrabajo por turnos
- ...contributing in a world-class manufacturing industry in Puerto Rico & USA. Responsibilities: Perform and/or review process validation [PV: characterization, OQ, PQ] (not cleaning process) and equipment qualification [CSV: URS, FAT, IQ, OQ, PQ, TMV] (not laboratory...SugeridoTrabajo por turnosFin de semana
- ...more information on surrogacy please see the documents on the left side of this page. In Texas, there is a judicial process for validating the Gestational Contract (the contract between the intended parents and the surrogate). Included within the various requirements...SugeridoTiempo completoContrato
- Perform, Qualification life cycle. Protocol & Report Change Control Generation Troubleshooting Experience in GMP workplace. Experience in Manufacturing and Packaging equipment.SugeridoContrato
- ...For Validation services in the Sterile and Filling area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Science or Engineering and a minimum of five (5) years of experience in the regulated industry. Excellent written and verbal skills...SugeridoContratoTurno de tardeTrabajo por turnos
- ...For Validation services in the Sterile and Filling area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Life Science or Engineering and a minimum of five (5) years of experience in the regulated industry. Excellent written and verbal skills...SugeridoContratoTurno de tardeTrabajo por turnos
- ...systems, lighting optimization, optics o Image acquisition and defect detection logic • Knowledge of AVI system qualification and validation: o IQ/OQ/PQ o Performance qualification using defect kits • Experience developing or supporting: o Inspection recipes...SugeridoDe duración determinadaTiempo completoTrabajo por turnos
- ...complexity. Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance, and/or validation departments. Work under the direct supervision of project managers to complete design, engineering, and construction projects...SugeridoContratoTrabajo por turnos
- ...troubleshooting. Implementation of system, equipment or process modifications, experiments, process and/or capital projects. Process Validation and Qualification. Inspection Systems, Visual Inspection, and Machine Vision. The Personality Part: ~ Picture...SugeridoContratoTrabajo por turnos
- ...systems, lighting optimization, optics Image acquisition and defect detection logic Knowledge of AVI system qualification and validation: IQ/OQ/PQ Performance qualification using defect kits Experience developing or supporting: Inspection recipes...SugeridoContratoTrabajo por turnos
- ...Summary of Role: With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance...SugeridoDe duración determinadaTiempo completoTrabajar en la oficinaRemotoTrabajo 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...SugeridoDe duración determinadaTiempo completoInicio inmediatoTrabajo por turnos
- ...troubleshooting mentorship. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications. Support the execution of...SugeridoContratoTurno de nocheTrabajo por turnos
- ...start-up of new equipment to ensure it meets all mechanical design specifications. Assist with the development and execution of validation documents for mechanical equipment. WHO WE ARE: We are a Service Provider company different from the rest. We pride...SugeridoContratoTrabajo por turnos
- ...indicators and operations. Work with manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for process and/or system modifications. Support the execution of...ContratoTurno de nocheTrabajo por turnosFin de semana
- ...Summary: Prepare and validate load files to support conversion and testing. Understand payroll system integrations to and from multiple vendors and sources. Key Responsibilities: Analyze, audit, reconcile, and resolve complex payroll processing and employee...Contrato
- ...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...Contrato
- ...Administrative shift (8 hours) Job Description: Support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance...Tiempo completoTrabajar en la oficinaTrabajo por turnos
- ...The Associate Quality Application Specialist supports the validation, administration, and compliance of quality-related computerized systems in a regulated environment. This role assists with validation documentation, system configuration, and cross-functional coordination...Contrato
- ...industry in Puerto Rico & USA. Responsibilities: Support the execution of manufacturing such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge...ContratoTrabajar en la oficinaTrabajo por turnos
- ...Summary The Quality Engineer II supports manufacturing and validation activities within a regulated medical device environment. This role is responsible for executing and reviewing process validations, equipment qualification, and computer system validation activities...ContratoTurno de mañanaTurno de tardeTrabajo por turnosFin de semana
- ...precision compared against established specifications and recommends and implements corrective action where necessary. Develops, validates, and implements controlled environment methods. Applies existing techniques and procedures with recommendations and...Tiempo completoTrabajo 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...ContratoTrabajo por turnos
- ...English Soft Skills: Excellent Communication skills, and Positive attitude. Shift: 1st Shift Experience in: Process Validation and Computer Software Validation. Technical writing knowledge Organization and communication Investigation and Root Cause...PrácticaContratoTrabajo por turnos
- ...Engineering (Electrical, Chemical, Computer, Mechanical, Industrial) and at least three (3) years of experience in Automation and Validation activities within the Medical Device or Pharmaceutical industry. Bilingual: Spanish and English (verbal/ written) Shift:...ContratoTrabajo por turnos
- ...Skills: Excellent teamwork skills Shift: 12-hour night shift , and according to business needs. Experience in: Process Validation (IQ/PD/OQ/PQ) Root cause analysis and problem resolution Technical writting The Personality Part: ~ Our Next Piece...ContratoTurno de nocheTrabajo por turnos
- ...Bachelor’s degree in Engineering ~1-3 years of Engineering experience in Medical Device industry ~ Root Cause Analysis ~ Process Validation (IQ/PD/OQ/PQ) ~ Technical Writing ~12 Hour Night Shift Quality Consulting Group, LLC is an equal opportunity employer,...TemporalTurno de noche
- ...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...ContratoTrabajo por turnos
- ...production control, product evaluation and reliability, as they apply to product or process quality. Performs and/or review process validation (not cleaning processes) and equipment documents: URS, FAT, IQ, OQ, PQ, TMV (not laboratory). Qualifications: Bachelor's...TemporalTurno de tardeTrabajo por turnosFin de semana