document

Provide operational support for document and records management activities at a pharmaceutical manufacturing site. Maintaining accurate, organized and readily retrievable GMP and business records to support day to day operations, regulatory compliance and inspection readiness. Working in accordance with Good Documentation Practices (GDP) and site procedures....

Document Controller, Puerto RicoMace combines global delivery consultancy experience to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us on our journey.You'll be responsible for:Defines and delivers IM strategies, standards and ISO *****-aligned...

Document Controller, Puerto RicoMace combines global delivery consultancy experience to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us on our journey.You'll be responsible for: * Defines and delivers IM strategies, standards and ISO...

Document Controller, Puerto RicoMace combines global delivery consultancy experience to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us on our journey.You'll be responsible for:Defines and delivers IM strategies, standards and ISO *****-aligned...

Document Controller, Puerto RicoMace combines global delivery consultancy experience to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us on our journey.You'll be responsible for: * Defines and delivers IM strategies, standards and ISO...

Provide operational support for document and records management activities at a pharmaceutical manufacturing site. Maintaining accurate, organized and readily retrievable GMP and business records to support day to day operations, regulatory compliance and inspection readiness. Working in accordance with Good Documentation Practices (GDP) and site procedures....

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, biotechnology, and medical device safety and efficacy guidelines. With offices...

Document Control Associate will ensure that all manufacturing documentation for medical devices are properly created, maintained, and compliant with regulatory standards.Responsibilities: * Ensure that all documents are up to date, accurate, and in compliance with relevant regulatory standards. * Assist in the creation of documents for product...

Job ID R-****** Date posted 30 March ****Job Description SummarySummary of Position with General Responsibilities:The Documentation Specialist will work with the Document Control Group Leader to achieve an efficient operation of the Document Control area, assisting area personnel as necessary. Coordinates with other departments to provide the necessary...

Job ID R-****** Date posted 30 March ****JOB DESCRIPTION SUMMARYSummary of Position with General Responsibilities:The Documentation Specialist will work with the Document Control Group Leader to achieve an efficient operation of the Document Control area, assisting area personnel as necessary. Coordinates with other departments to provide the necessary...

I. Título de la Posición: Oficial Registro de DocumentosClasificación: No ExentoDepartamento: Manejo de Casos Reporta: Jefe de grupo de Manejo de CasosII. RESUMEN DEL PUESTOEl puesto de Oficial de Registro de Documentos tiene como propósito fungir como agente distribuidor de la compañía en el proceso de recibir toda la información necesaria...

Job ID R-****** Date posted 30 March ****Job Description SummarySummary of Position with General Responsibilities:The Documentation Specialist will work with the Document Control Group Leader to achieve an efficient operation of the Document Control area, assisting area personnel as necessary. Coordinates with other departments to provide the necessary...

Job ID R-****** Date posted 30 March ****JOB DESCRIPTION SUMMARYSummary of Position with General Responsibilities:The Documentation Specialist will work with the Document Control Group Leader to achieve an efficient operation of the Document Control area, assisting area personnel as necessary. Coordinates with other departments to provide the necessary...

I. Título de la Posición: Oficial Registro de DocumentosClasificación: No ExentoDepartamento: Manejo de Casos Reporta: Jefe de grupo de Manejo de CasosII. RESUMEN DEL PUESTOEl puesto de Oficial de Registro de Documentos tiene como propósito fungir como agente distribuidor de la compañía en el proceso de recibir toda la información necesaria...

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, biotechnology, and medical device safety and efficacy guidelines. With offices...

For Documentation services in the Quality areaWHAT MAKES YOU A FIT:The Technical Part:Bachelor's Degree and previous experience in compliance and/or document control activities within the Pharmaceutical or Medical Devices industry.Excellent reading, writing, and speaking skills in Spanish and English.Shift: Administrative, and according to business...

Document Control Associate will ensure that all manufacturing documentation for medical devices are properly created, maintained, and compliant with regulatory standards.*Responsibilities:** Ensure that all documents are up to date, accurate, and in compliance with relevant regulatory standards.* Assist in the creation of documents for product...

For Documentation services in the Quality areaWHAT MAKES YOU A FIT:The Technical Part: * Bachelor's Degree and previous experience in compliance and/or document control activities within the Pharmaceutical or Medical Devices industry. * Excellent reading, writing, and speaking skills in Spanish and English. * Shift: Administrative, and according to business...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.We are seeking a talented, dedicated...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.We are seeking a talented, dedicated...