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- ...Experiencia en calidad Asociado en Ciencia Conocimiento en la industria de materia prima Capacidad para trabajar en ambiente de calor y polvo Conocimiento de idioma inglés Experiencia en documentación y manejo de programas de computadoras Enviar resume a: ******...Sugerido
- ...Expertise Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner. Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement...SugeridoTiempo completoContratoTrabajo por turnos
- ...Cyber Operations Specialist – Vulnerability Assessment Management General Description The Cybersecurity Vulnerability Specialist... ...to strengthen assessment capabilities. Reporting & Documentation Produce clear, detailed technical reports that describe vulnerabilities...SugeridoPrácticaPatrocinio de visaInicio inmediatoTrabajo híbrido
- ...Identify recurring issues and opportunities to improve remediation workflows, processes and tooling. Ensure remediations evidence is documented. Maintain dashboards and reporting on remediation status, aging risks, and trends. Support risk assessments evaluating...SugeridoPrácticaPatrocinio de visaInicio inmediatoTrabajo híbrido
- ...about our services and solutions! Job Description Validation Specialist with a strong knowledge of injection molding processes to support the development, execution, and documentation of validation activities (Protocols, Tests, Reports). Familiarized with...SugeridoContrato
- ...bring on Full Time- Grants Management Specialist II (GMS II) to join our team. The Grants... ...applications, reimbursement requests, reporting, documentation management, eligibility reviews,... ...level. Provided IT tools and document management tools to create, organize and...SugeridoContratistaTiempo completoTrabajar en la oficina
- ...execute validation protocols and reports in accordance with GMP and company standards. Generate and maintain change control documentation for equipment and process modifications. Perform t roubleshooting and root cause analysis for validation-related issues....SugeridoContratoTrabajo por turnos
- ...the job) Conducts a compliant validation process for quality information technology systems, which requires formal validation documentation. Coordinates activities with clients, programmers/developers, and operating personnel, domestic and, as appropriate, global....SugeridoContratoTrabajo por turnos
- ...business needs. Experience in: Validation (OQ/PQ/TMV/IPM) Validation lifecycle and documentation Regulated environments (FDA, ISO, GMP) Data analysis tools Document management systems The Personality Part: ~ Our Next Piece is someone who treats...SugeridoTrabajo por turnos
- ...IEM is searching for a Full Time- Data Analyst and Reporting Specialist to provide data analytics and reporting support to IEM's Disaster... ...to ensure data integrity and performance. * Outline and document data requirements and reporting needs for clients, programs, and...SugeridoTiempo completoTrabajar en la oficinaTrabajo por turnos
- ...collaborate with technical and management staff within manufacturing, process development, and quality. Proficiency in GDP (Good Documentation Practices) on a regulated environment Knowledge in systems/Tools: Trackwise, VEEVA, MES, Smart Sheet, ChatGPT, Copilot, Power...SugeridoContrato
- ...all events being conducted in the store. Assists other Event Specialists with event kits, materials and tools as needed. * Assist Supervisor... .... * Takes digital photos of Perfect Table Setup to document success stories for clients. This role is not expected to exceed...SugeridoPor horaTiempo parcial
- Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical...SugeridoTiempo completo
- Bachelor's degree in engineering is a plus Deviations management Deviation assessments Track wise Biotech and manufacturing experience Requirements Doctorate OR Master’s + 2 years of Manufacturing Operations experience Alternatively, Bachelors + ...SugeridoContratoTrabajo por turnos
- ...We are looking for an experienced Investigation Specialist to join a centralized team responsible for conducting investigations related... ...investigations. Perform investigations of QA events and document findings according Requirements Bachelor’s degree in a scientific...SugeridoContrato
- ...( A summary of the purpose of the position) Our Compliance Specialist will perform administrative tasks to ensure all compliance functions... .... Generate product certificate of compliance or test documents for required customer orders. Work with all necessary internal...Tiempo completoContratoTrabajar en la oficina
- ...OVERVIEW: We are seeking an Accounts Receivable Collection Specialist to join our Accounting team. This position requires knowledge... ...for accounts receivable Support audits by providing AR documentation as required What You’ll Have: ~2+ years of accounts receivable...Tiempo completoTrabajar en la oficina
- ...cleaning validation protocols using Kneat and Tulip platforms , while enhancing data integrity requirements and improving existing documentation and processes. 1. Active participation on Cleaning Validation team meetings to provide input on projects timeline...PrácticaContrato
- ...As the BioA Reagents & Consumables Specialist, you will be responsible for Reagents and Consumables sales to mid-size and large accounts... ...-on experience with SFDC or comparable CRM tools with strong documentation discipline Willingness and ability to travel frequently...CASTrabajar en la oficinaRemotoHorario flexible
- ...reports and environmental/CU data to identify areas for improvement ~ Hands on experience in electronic systems for instance: Documentation platforms such as Veeva, Spotfire, LIMS, Maximo. ~ Use of artificial intelligence tools such as data analytics and large language...ContratoTrabajo por turnos
- For Product Development Project Management services in the Manufacturing area WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s degree in Engineering/Business Administration and a minimum of five (5) years of exposure within the Medical Devices or Pharmaceutical...ContratoTrabajo híbridoTrabajo por turnos
$17 - $20 por hora
Responsible for executing, monitoring, and training inventory best practices and standard operating procedures for the entire store, including both front end and pharmacy. Supports pharmacy inventory management activities, including receiving, counting, ordering, and facilitating...Turno de tardeTrabajo por turnos- Education: Associate or Bachelor's degree in a computer-related field with 3-5 years of related experience. Minimum Years of Experience: 3-5 year in related experience Certifications: CompTIA CySA+ (plus) Required Technologies Experience...Trabajar en la oficina
- *Title: Validation Specialist III - ***** (Añasco)**Job Type*: Professional services contract... ...*: * Plans, develops, and implements documentation, procedures, and trainings necessary... ...criteria. Evaluate, investigate and document non-conformances incidents and/or protocol...Por horaContratistaTiempo completoContratoFin de semana
- Educational background preferred: Science, Engineering Experience in Manufacturing area working with procedures. CAPA/ CAPA EV, Change Control, develop new procedures, enhance currents process, Implement new process, modify the current SOP’s, Provide training to...ContratoTrabajo por turnos
- ...Description We are seeking a SAP Implementation Support Specialist to support the deployment of SAP within a regulated medical... ...(production, quality, warehouse) Create compliant documentation: Work Instructions (WIs), SOPs Job aids and training materialsm...ContratoTrabajo por turnos
- ...The Quality Application Specialist supports quality and product transfer activities within a regulated medical device manufacturing... ...regulatory requirements. Develop, review, and maintain validation documentation, including SOPs, validation plans, protocols, reports, and...ContratoTrabajo por turnosFin de semana
- ...The Senior IT Specialist is responsible for the administration, maintenance, monitoring, troubleshooting, and continuous improvement... ...network, and security upgrades Develop and maintain technical documentation, procedures, and knowledge base articles Participate in...Trabajar en la oficinaRemotoTrabajo híbrido
- ...Bilingual (Spanish and English) Shift: Administrative & according to business needs Experience in: EU MDR and Medical Device Documentation Gap Assessments and Compliance Reviews Execution of Remediation and Validation Activities The Personality Part: ~...ContratoTrabajo por turnos
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world...Trabajar en la oficinaRemoto