Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr
Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Coordinator II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than
Salary Range:21.700,00 € - 40.300,00 € Job Description SummaryThe Equipment Operator ensures the execution of secondary packaging activities for ophthalmic products in compliance with GMP regulations, company procedures, and established quality, safety, and productivity requirements. Job
Salary Range:26.000,00 € - 48.400,00 € Job Description SummaryThe Equipment Specialist ensures the reliability, availability, and GMP compliance of the electronic, electrical, and automation systems installed on secondary packaging lines for ophthalmic products. The role is
Adecco Italia Spa cerca addetti/e al controllo qualità e confezionamento di abbigliamento di lusso presso Landriano (Lombardia). Le attività includono confezionamento, imballaggio e controllo qualità visivo; è richiesto impegno e manualità, con turni dal lunedì alla
Specific activities and responsibilities: - Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment - Preparation of validation protocols, reports and related documentation. - knowledge of GMP regulations - Ensure compliance
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipmentPreparation of validation protocols, reports and related documentation.knowledge of GMP regulationsEnsure compliance with GMP requirements and internal quality standards.Support
Tecnimont, società leader del gruppo MAIRE per le soluzioni integrate E&C, presente in numerosi Paesi, è una realtà consolidata e di riferimento nel settore dei servizi innovativi di ingegneria e costruzione, impegnata a realizzare le infrastrutture
Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary Of Responsibilities Responsible for all
About Us ProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as: Product Development, Market & Patient Access, Regulatory Affairs and Safety & Vigilance
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Job Function: Quality Job Sub Function: Quality Assurance Job Category: Business Enablement/Support All Job Posting Locations: Latina, Italy Job Description: At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to
Job Overview:The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA
Position Summary We are looking for a candidate that will join our team as a QC Laboratory Technician. The QC Laboratory Technician is responsible for assisting in administration of the quality functions at a site to assure adherence
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and
QA/QC Mechanical-Piping | Oil & GasLe informazioni riportate di seguito illustrano i requisiti del ruolo, lesperienza richiesta ai candidati e le qualifiche associate.Per importante progetto nel settore Oil & Gas, siamo alla ricerca di un QA/QC Mechanical-Piping con almeno
At Bryden Wood, we are expanding our team in Milan to work on large scale projects for the biggest names in Big Tech and Pharmaceutical sectors. We are looking for an Associate Electrical Engineer to lead the