Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
Overview The Sr. Specialist, Computer System Validation (CSV), Quality is responsible for managing and supporting Computer System Validation activities for GxP global computerized systems, ensuring compliance with applicable regulatory requirements, industry standards and Alfasigma Quality Policies and Procedures. The role contributes to
Alfasigma is seeking a Sr. Specialist for Computer System Validation in Pomezia, Italy. This role is integral to managing and supporting validation activities for GxP global computerized systems, ensuring compliance with regulatory standards. Candidates should have 5-7 years of experience in
Overview The Sr. Specialist, Computer System Validation (CSV), Quality is responsible for managing and supporting Computer System Validation activities for GxP global computerized systems, ensuring compliance with applicable regulatory requirements, industry standards and Alfasigma Quality Policies and Procedures. The role contributes to
About usChiesi is an international research-focused biopharmaceutical group with 90 years experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular
ResponsibilitiesThe new employee, reporting directly to the Quality Validation Coordinator, will be part of a team of 4 people. As a Quality Validation Specialist, they will play a crucial role in ensuring compliance with GMP requirements by supporting
Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
Responsibilities The new employee, reporting directly to the Quality Validation Coordinator, will be part of a team of 4 people. As a Quality Validation Specialist, they will play a crucial role in ensuring compliance with GMP requirements by
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
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several
Fortil is an international engineering and technology consulting group built on an independent model, bringing together over 2,500 employees. With 30 offices across 14 countries, Fortil fosters entrepreneurial freedom and the empowerment of individual potential. We
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives
Job Description The QA Digital Compliance Manager is responsible for ensuring that all digital systems, records, instruments, processes and data handling within operations adhere to relevant regulatory, legal, best practices and industry standards. Key Responsibilities Monitoring and
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on