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
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 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
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 equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and
Job descriptions may display in multiple languages based on your language selection. What We Offer At Magna, you can expect an engaging and dynamic environment where you can help to develop industry-leading automotive technologies. We invest