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- ...our well-established clients in the healthcare industry is seeking an experienced physician executive to join its leadership team as Medical Vice President. This executive will provide strategic clinical leadership and operational oversight across multiple healthcare...SugeridoTiempo completo
- ...the Interpreters code of conduct. Be aware of the specific vocabulary of the industry the interpreter works with (healthcare and medical, specifically). Go into internal professional training. Communicate and report to your team leader. YOUR BACKGROUND AND...SugeridoTrabajo remotoTiempo completoInicio inmediato
- · Bachelor's degree in Mechanical, Electrical, Industrial, Manufacturing, Biomedical Engineering, or related technical field. ·5-7+ years in manufacturing engineering, process engineering, validation engineering, or quality engineering within an FDA-regulated environment...SugeridoContrato
- · knowledge of 21 CFR Part 820, GMP, ISO 13485, and documentation practices required in regulated manufacturing environments. · Electrical and mechanical engineering background applied to automated or semi-automated manufacturing systems. · knowledge of automation...SugeridoContrato
- Support multiple new line development projects by executing Tool Qualifications (TQFs), Operational Qualification (OQ), Performance Qualification (PQ), Test Method Validation (TMV), and In-Process Monitoring (IPM) by leveraging automated tools and site-level expertise...SugeridoContrato
- ...environments. • Familiarity with FAA governance, cybersecurity protocols, and safety regulations. • Certifications such as ETA... ...Benefits offered to all employees who work 30+ hours per week: Medical, Dental, Vision, Life Insurance, Short-Term Disability, Long-Term...SugeridoPor horaContratistaTemporalTiempo completoContratoTrabajar en la oficinaRemoto
- ...Process Validation. Writing technical protocols or reports. The Personality Part:... ...conducted in compliance with the respective protocol and applicable guidelines and... ...being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients...SugeridoContratoTrabajo por turnos
- ...than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients... ...addition, a Sterilization Microbiologist II will contribute to protocol and report writing, risk assessments, and continuous improvement...SugeridoPrácticaTemporalTrabajar en la oficinaInicio inmediato
- ...is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory... ...manufacturing site. Selected candidates may support QA oversight, protocol review and approval, CAPA, deviation investigations,...SugeridoContrato
- ...environments — escorts, training, GMP gowning, restricted-zone protocols. Drive HSE and quality compliance in live-plant conditions;... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality...SugeridoContratistaContratoTrabajo por turnos
- ...is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory... ...depending on project need. The role includes authoring and executing protocols, supporting field execution, documenting results, resolving...SugeridoContrato
- ...is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory... ...Key Responsibilities Support the execution of validation protocols for Molding processes and equipment. Collect, analyze, and document...SugeridoContrato
- ...degree in Engineering with (3) years within the Pharmaceutical or Medical Device Industry. Shift: Administrative and according to... ...documents. Support any method transfer, verification and validation protocols. Works with document owner to make appropriate revision....SugeridoContratoTrabajo por turnos
- ...activities within the Pharmaceutical & Medical Devices Industry. Bilingual: Spanish... ...Develop, execute, and document validation protocols and reports, including Installation Qualification... ...and recommendations. Support protocol deviations, investigations, corrective...SugeridoContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented,... ..., and campaign readiness activities. Generate technical protocols and related documentation as required. Support the creation...SugeridoContratoTrabajo por turnos
- ...is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory... ...and documentation processes in a highly regulated environment. Protocol Development and execution requirements. Additional Information...Contrato
- ...activities within the Pharmaceutical or Medical Devices industry. , Bilingual (Spanish... ...Matrices, FAT/SAT, IQ/OQ/PQ protocols, and Validation Reports. Participate... ...requirements gathering, risk assessments, protocol development, testing execution, deviation...ContratoTrabajo por turnos
- ...support for day-to-day manufacturing operations within a regulated medical device manufacturing environment. This role serves as the... ...engineering study, qualification, validation, and verification protocols and reports with minimal supervision. Support equipment, process...Tiempo completo
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented,... ...with generation and the implementation of process validation protocols and reports. Participate in regulatory inspections...ContratoTrabajo por turnos
- ...Experie nce in: Generation & Execution Protocols Commissioning, Qualification, and... ...Commissioning Qualification, Technical Writing, Protocol Drafting. Review and Execution of... ..., while providing our Pharmaceutical, Medical Device and Manufacturing industry...ContratoTrabajo por turnos
- ...Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality...ContratoTrabajo por turnos
- ...of 5-8 years of engineering experience within Pharmaceutical, Medical Device, Biotechnology, or Chemical Manufacturing environments.... ...manufacturing environments. Experience with IQ/OQ/PQ validation protocols and equipment commissioning. Knowledge of Statistical...ContratistaTemporal
- ...Engineer to support manufacturing operations within a regulated Medical Device or Pharmaceutical environment. The selected candidate... ...Generate, execute, review, and approve qualification and validation protocols and reports with minimal supervision. Serve as the technical...ContratistaTemporal
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented,... ...major changes, or campaign readiness. Generate technical protocols as needed. Assist and provide guidance during MBR (Master Batch...Contrato
- ...Engineer to support a product transfer project within a regulated medical device manufacturing environment. The ideal candidate will have... ...Qualification (PQ) Generate technical reports, validation protocols, and engineering documentation. Analyze manufacturing...Temporal
- ...of new equipment process. Engineering Project. Validation Protocols. AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch...ContratoTrabajo por turnos
- ...patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements. Your Profile: You will bring... ...of ICH-GCP guidelines and the expertise to review and evaluate medical data Excellent written and verbal communication in English...Tiempo completoTrabajo híbrido
- ...For Validation services in the Project Engineeirng/Medical Device Packaging area. WHAT MAKES YOU A FIT: The Technical Part:... ...Engineering documentation, data collection, technical reports, protocols, specifications, and change records. Manufacturing processes...ContratoTrabajo por turnosFin de semana
- ...consecutive, first-person interpretation. Follows interpreter protocols and procedures as required by Propio L.S. clients. Follows... ...subject matter knowledge, as required for various clients, such as medical, legal, social services, etc. Requirements: Submission of...ContratoRemoto
- ...proven experience in commissioning and qualification processes, protocol generation and execution. Bilingual (Spanish and English.)... ...our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch...ContratoTrabajo por turnos